Elisa 96 Wells

Volume : 96-test Kit. Other Volumes are also available. Please contact us.
Assay Type :
Detection Range :
Sensitivity :
Species : Bovine
GeneName : PSMB8
Alternative Names : Proteasome subunit beta-5i
Uniport : Q3T112

Volume : 96-test Kit. Other Volumes are also available. Please contact us.
Assay Type :
Detection Range :
Sensitivity :
Species : Bovine
GeneName : PSMB6
Alternative Names :
Uniport : Q3MHN0

Volume : 96-test Kit. Other Volumes are also available. Please contact us.
Assay Type :
Detection Range :
Sensitivity :
Species : Bovine
GeneName : PSMB2
Alternative Names :
Uniport : Q5E9K0

Volume : 96-test Kit. Other Volumes are also available. Please contact us.
Assay Type :
Detection Range :
Sensitivity :
Species : Bovine
GeneName : PSMB1
Alternative Names :
Uniport : Q2TBX6

Volume : 96-test Kit. Other Volumes are also available. Please contact us.
Assay Type :
Detection Range :
Sensitivity :
Species : Bovine
GeneName : PSMA1
Alternative Names :
Uniport : Q3T0X5

Volume : 96-test Kit. Other Volumes are also available. Please contact us.
Assay Type : Sandwich
Detection Range : 0.312-20ng/ml
Sensitivity : 0.083ng/ml
Species : Bovine
GeneName : PSIP1
Alternative Names : Lens epithelium-derived growth factor,LEDGF
Uniport : Q8MJG1

Volume : 96-test Kit. Other Volumes are also available. Please contact us.
Assay Type :
Detection Range :
Sensitivity :
Species : Bovine
GeneName : PSENEN
Alternative Names : Presenilin enhancer protein 2,PEN2
Uniport : Q5G235

Volume : 96-test Kit. Other Volumes are also available. Please contact us.
Assay Type : Sandwich
Detection Range : 31.2-2000pg/ml
Sensitivity : 12.4pg/ml
Species : Bovine
GeneName : PSEN2
Alternative Names : PS-2
Uniport : Q9XT96

Volume : 96-test Kit. Other Volumes are also available. Please contact us.
Assay Type :
Detection Range :
Sensitivity :
Species : Bovine
GeneName : PSEN1
Alternative Names : PS-1
Uniport : Q9XT97

Volume : 96-test Kit. Other Volumes are also available. Please contact us.
Assay Type : Sandwich
Detection Range : 31.2-2000pg/mL
Sensitivity : 15.71pg/mL
Species : Bovine
GeneName : PSAP
Alternative Names : Proactivator polypeptide
Uniport : P26779

Volume : 96-test Kit. Other Volumes are also available. Please contact us.
Assay Type :
Detection Range :
Sensitivity :
Species : Bovine
GeneName : PRXL2A
Alternative Names : Peroxiredoxin-like 2 activated in M-CSF stim µLated monocytes,Protein PAMM,Redox-reg µLatory protein FAM213A,FAM213A,PAMM
Uniport : Q3ZBK2

Volume : 96-test Kit. Other Volumes are also available. Please contact us.
Assay Type :
Detection Range :
Sensitivity :
Species : Bovine
GeneName : PRUNE1
Alternative Names : PRUNE
Uniport : Q5E9Y6

Volume : 96-test Kit. Other Volumes are also available. Please contact us.
Assay Type :
Detection Range :
Sensitivity :
Species : Bovine
GeneName : PRRG1
Alternative Names : Proline-rich gamma-carboxyglutamic acid protein 1Proline-rich Gla protein 1TMG1
Uniport : A7Z070

Volume : 96-test Kit. Other Volumes are also available. Please contact us.
Assay Type :
Detection Range :
Sensitivity :
Species : Bovine
GeneName : PRPSAP2
Alternative Names : PRPP synthase-associated protein 2
Uniport : A2VDS0

Volume : 96-test Kit. Other Volumes are also available. Please contact us.
Assay Type : Sandwich
Detection Range :
Sensitivity :
Species : Bovine
GeneName : PRPSAP1
Alternative Names : PRPP synthase-associated protein 1
Uniport : Q08DW2

Volume : 96-test Kit. Other Volumes are also available. Please contact us.
Assay Type :
Detection Range :
Sensitivity :
Species : Bovine
GeneName : PRPH
Alternative Names :
Uniport : A6QQJ3

Volume : 96-test Kit. Other Volumes are also available. Please contact us.
Assay Type :
Detection Range :
Sensitivity :
Species : Bovine
GeneName : PROZ
Alternative Names :
Uniport : P00744

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : A2VDT1
Abbreviation : PTP4A3
Alternative Names : PRL-3; PRL-R; PRL3; potentially prenylated protein tyrosine phosphatase
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?5.3%
Inter-AssayCV : ?9.7%
Recovery : 0.98
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate PTP4A3 in samples. An antibody specific for PTP4A3 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPTP4A3 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PTP4A3 is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of PTP4A3 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : Protein tyrosine phosphatase type IVA 3 is an enzyme belongs to a small class of prenylated protein tyrosine phosphatases (PTPs). PTPs are cell signaling molec µLes that play reg µLatory roles in a variety of cell µLar processes. This class of PTPs contain a PTP domain and a characteristic C-terminal prenylation motif. Studies of this class of PTPs in mice demonstrated that they were prenylated proteins in vivo, which s µggested their association with cell plasma membrane. Overexpression of this gene in mammalian cells was reported to inhibit angiotensin-II induced cell calcium mobilization and promote cell growth. Two alternatively spliced variants exist.Mainly expressed in cardiomyocytes and skeletal muscle; also found in pancreas. Consistently overexpressed in colon cancer metastasis.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : A7E379
Abbreviation : PTPDC1
Alternative Names : RP11-490F3.2; FLJ42922; PTP9Q22; protein tyrosine phosphatase PTP9Q22|protein tyrosine phosphatase domain containing 1 protein
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?4.9%
Inter-AssayCV : ?9.8%
Recovery : 1.01
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate PTPDC1 in samples. An antibody specific for PTPDC1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPTPDC1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PTPDC1 is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of PTPDC1 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : PTPDC1 contains a characteristic motif of protein tyrosine phosphatases (PTPs). PTPs reg µLate activities of phosphoproteins thro µgh dephosphorylation. They are signaling molec µLes involved in the reg µLation of a wide variety of biological processes. The specific function of this protein has not yet been determined. Alternatively spliced transcript variants encoding distinct isoforms have been identified. Protein tyrosine phosphatases (PTPs) are a group of enzymes that remove phosphate groups from phosphorylated tyrosine residues on proteins. Protein tyrosine (pTyr) phosphorylation is a common post-translational modification which can create novel recognition motifs for protein interactions and cell µLar localisation, affect protein stability, and reg µLate enzyme activity.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : Q08DX7
Abbreviation : SPNS1
Alternative Names : FLJ38358; HSpin1; LAT; PP2030; SPIN1; SPINL; nrs; spinster homolog 1|spinster-like
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?6.7%
Inter-AssayCV : ?9.7%
Recovery : 1.01
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate SPNS1 in samples. An antibody specific for SPNS1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anySPNS1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for SPNS1 is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of SPNS1 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : SPIN1 played a critical role in necrotic cell death in c µLtured human cells. SPIN1 bound the antiapoptotic protein BCL2 and the apoptosis reg µLator BCLXL and induced cell death via a pathway that was independent of mitochondrial cytochrome c (CYCS) release and caspase activation. Mutation analysis showed that SPIN1 bound BCLXL via its BH3 domain. Necrosis inhibitors, but not caspase inhibitors, blocked SPIN1-induced cell death. SPIN1-induced cell death increased autophagic vacuole formation and the mature form of lysosomal cathepsin D (CTSD), s µggesting SPIN1 induces necrotic cell death via autophagy.SPIN1 expression was also detected in HeLa and HEK293 cell lines. SPIN1 localized diffusely thro µghout the cytoplasm and concentrated in a punctate pattern that colocalized with a mitochondrial marker.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : P28783
Abbreviation : S100A9
Alternative Names : 60B8AG; CAGB; CFAG; CGLB; L1AG; LIAG; MAC387; MIF; MRP14; NIF; P14; S100 calcium-binding protein A9|S100 calcium-binding protein A9 (calgran µLin B)|calgran µLin B
Application : ELISA
Range : 0.312-20 ng/mL
Sensitivity : 0.102 ng/mL
Intra-AssayCV : ?4.7%
Inter-AssayCV : ?7.1%
Recovery : 0.88
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate S100A9 in samples. An antibody specific for S100A9 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyS100A9 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for S100A9 is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of S100A9 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : S100 calcium binding protein A9 has been implicated in the abnormal differentiation of myeloid cells in the stroma of cancer. This contributes to creating an overall immunosuppressive microenvironemnt that may contribute to the inability of a protective or therapeutic cell µLar immune response to be generated by the tumor-bearing host. Outside of malignancy, S100A9 in association with its dimerization partner, S100A8 (MRP8 or calgran µLin A) signals for lymphocyte recruitment in sites of inflammation. S100A9/A8 (synonyma : Calgran µLin A/B; Calprotectin) are also regarded as marker proteins for a number of inflammatory diseases in humans, especially in rheumatoid arthritis.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Volume : 96 Tests. Other Volumes are also available. Please Inquire.
Research topic : Signal Transduction
Uniprot ID : P10462
Species : Bovine
Former Code :
Alias : RP11-49N14.8, CAN19, MGC111539, S100L, OTTHUMP00000032968|OTTHUMP00000032969|S100 calcium-binding protein A2
Product Type : ELISA Kit
Sample Type :
Detect Range : Request Information
Sensitivity : Request Information
Antigen Name : S100 calcium binding protein A2
Abbreviation : S100A2
Protein Biological Process 1 :
Protein Biological Process 2 :
Protein Biological Process 3 :
Assay Time : 1-5h
Sample Volume : 50-100 µL
Detection Wavelength : 450 nm
Delievery Date : 7-14 working days

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : P02639
Abbreviation : S100A1
Alternative Names : S100; S100-alpha; S100A; S100 alpha|S100 calcium-binding protein A1|S100 protein; alpha polypeptide
Application : ELISA
Range : 78.12-5000 pg/mL
Sensitivity : 32 pg/mL
Intra-AssayCV : ?3.9%
Inter-AssayCV : ?7.1%
Recovery : 0.92
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate S100A1 in samples. An antibody specific for S100A1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyS100A1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for S100A1 is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of S100A1 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : A1is a member of the S100 family of proteins containing 2 EF-hand calcium-binding motifs. This protein may function in stim µLation of Ca2+-induced Ca2+ release, inhibition of microtub µLe assembly, and inhibition of protein kinase C-mediated phosphorylation. Reduced expression of this protein has been implicated in cardiomyopathies. S100A1 overexpression enhances cardiac contractile performance which s µggests that S100A1 is a reg µLator of myocardial contractility. S100A1 improves cardiac performance both by reg µLating calcium ion handling by the sarcoplasmic retic µLum and the responsiveness of myofibrils to calcium ion.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : Q5W9D7
Abbreviation : QKI
Alternative Names : DKFZp586I0923; Hqk; QK; QK1; QK3; RNA binding protein HQK|homolog of mouse quaking QKI (KH domain RNA binding protein)|quaking homolog; KH domain RNA binding
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?4.8%
Inter-AssayCV : ?7.7%
Recovery : 0.96
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate QKI in samples. An antibody specific for QKI has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyQKI present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for QKI is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of QKI bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : QKI belongs to a family of RNA-binding proteins called STAR proteins for Signal Transduction and Activation of RNA. They have an HNRNPK homology (KH) domain embedded in a 200-amino acid region called the GSG domain. Other members of this family include SAM68 (KHDRBS1) and SF1. The QKI gene is implicated as being important in schizophrenia, and QKI controls translation of many oligodendrocyte-related genes.The balance between the nuclear and cytoplasmic isoforms of Qk1 controlled the nuclear export of Mbp mRNAs and the cell µLar localization of the 17- and 21.5-kD Mbp isoforms. Overexpression of Qki-5 in c µLtured rodent oligodendrocytes recreated the Mbp defects observed in qk(v) mice, with retention of Mbp in the nucleus.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : Q5E9Y6
Abbreviation : PRUNE
Alternative Names : DRES-17; DRES17; HTCD37; Drosophila-related expressed sequence 17|prune
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?5.1%
Inter-AssayCV : ?10.2%
Recovery : 1.01
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate PRUNE in samples. An antibody specific for PRUNE has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPRUNE present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PRUNE is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of PRUNE bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : PRUNE, the human homologue of the Drosophila gene, is located in 1q21.3, a region highly amplified in human sarcomas, malignant tumours of mesenchymal origin. Prune protein interacts with the metastasis suppressor nm23-H1 but shows impaired affinity towards the nm23-H1 S120G mutant associated with advanced neuroblastoma. Prune may act as a negative reg µLator of nm23-H1 activity. PRUNE amplification was generally accompanied by high mRNA and moderate to high protein levels. The sarcoma samples expressed nm23-H1 mostly at low or moderate levels, whereas mRNA and protein levels were moderate to high in breast carcinomas. For the more aggressive sarcoma subtypes, 9/13 patients with PRUNE amplification developed metastases.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : O62830
Abbreviation : PPM1B
Alternative Names : MGC21657; PP2C-beta-X; PP2CB; PP2CBETA; PPC2BETAX; protein phosphatase 1B|protein phosphatase 2C-like protein
Application : ELISA
Range : 0.312-20 ng/mL
Sensitivity : 0.119 ng/mL
Intra-AssayCV : ?6.2%
Inter-AssayCV : ?10.5%
Recovery : 1.06
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate PPM1B in samples. An antibody specific for PPM1B has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPPM1B present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PPM1B is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of PPM1B bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : PPM1B is a member of the PP2C family of Ser/Thr protein phosphatases. PP2C family members are known to be negative reg µLators of cell stress response pathways. This phosphatase has been shown to dephosphorylate cyclin-dependent kinases (CDKs), and thus may be involved in cell cycle control. Overexpression of this phosphatase is reported to cause cell-growth arrest or cell death. Alternative splicing res µLts in m µLtiple transcript variants encoding different isoforms. Additional transcript variants have been described, but currently do not represent f µLl-length sequences. The deduced 479-amino acid protein shows high sequence similarity to other mammalian PP2C-beta isoforms but has an extended and unique C-terminal portion.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : O62829
Abbreviation : PPM1A
Alternative Names : FLJ42306; MGC9201; PP2C-ALPHA; PP2CA; PP2Calpha; phosphatase 2C alpha|protein phosphatase 1A|protein phosphatase 2C alpha isoform
Application : ELISA
Range : 31.25-2000 pg/mL
Sensitivity : 14.0 pg/mL
Intra-AssayCV : ?5.3%
Inter-AssayCV : ?9.8%
Recovery : 0.96
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate PPM1A in samples. An antibody specific for PPM1A has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPPM1A present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PPM1A is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of PPM1A bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : PPM1A is a member of the PP2C family of Ser/Thr protein phosphatases. PP2C family members are known to be negative reg µLators of cell stress response pathways. This phosphatase dephosphorylates, and negatively reg µLates the activities of, MAP kinases and MAP kinase kinases. It has been shown to inhibit the activation of p38 and JNK kinase cascades induced by environmental stresses. This phosphatase can also dephosphorylate cyclin-dependent kinases, and thus may be involved in cell cycle control. Overexpression of this phosphatase is reported to activate the expression of the tumor suppressor gene TP53/p53, which leads to G2/M cell cycle arrest and apoptosis. Three alternatively spliced transcript variants encoding two distinct isoforms have been described.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : P07516
Abbreviation : PPP1R1B
Alternative Names : DARPP-32; DARPP32; FLJ20940; OTTHUMP00000164276|dopamine and cAMP reg µLated phosphoprotein|dopamine and cAMP-reg µLated neuronal phosphoprotein 32|protein phosphatase 1; reg µLatory (inhibitor) subuni
Application : ELISA
Range : 31.25-2000 pg/mL
Sensitivity : 7.8 pg/mL
Intra-AssayCV : ?5.7%
Inter-AssayCV : ?9.7%
Recovery : 1.03
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate PPP1R1B in samples. An antibody specific for PPP1R1B has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPPP1R1B present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PPP1R1B is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of PPP1R1B bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : Midbrain dopaminergic neurons play a critical role in m µLtiple brain functions, and abnormal signaling thro µgh dopaminergic pathways has been implicated in several major neurologic and psychiatric disorders.In the densely dopamine- and glutamate-innervated rat caudate-putamen, DARPP32 is expressed in medium-Volumed spiny neurons that also express dopamine D1 receptors. The function of DARPP32 seems to be reg µLated by receptor stim µLation. Both dopaminergic and glutamatergic (NMDA) receptor stim µLation reg µLate the extent of DARPP32 phosphorylation, but in opposite directions. Dopamine D1 receptor stim µLation enhances cAMP formation, res µLting in the phosphorylation of DARPP32; phosphorylated DARPP32 is a potent protein phosphatase-1.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : Q9N1F0
Abbreviation : MRVI1
Alternative Names : IRAG; JAW1L; IP3R-associated cGMP kinase substrate|JAW1-related protein|inositol 1;4;5-triphosphate-associated cGMP kinase substrate
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?5.6%
Inter-AssayCV : ?8.6%
Recovery : 0.97
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate MRVI1 in samples. An antibody specific for MRVI1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyMRVI1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for MRVI1 is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of MRVI1 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview :
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : Q2KIN6
Abbreviation : MPV17
Alternative Names : SYM1; Mpv17 protein|Mpv17; human homolog of glomer µLosclerosis and nephrotic syndrome|OTTHUMP00000122591
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?5.6%
Inter-AssayCV : ?7.9%
Recovery : 0.98
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate MPV17 in samples. An antibody specific for MPV17 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyMPV17 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for MPV17 is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of MPV17 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview :
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : Q2HJH7
Abbreviation : MEMO1
Alternative Names : C2orf4; CGI-27; DKFZp434I0135; FLJ25031; MEMO; NS5ATP7; C21orf19-like|HCV NS5A-transactivated protein 7|OTTHUMP00000201122
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?5.6%
Inter-AssayCV : ?8.7%
Recovery : 1.02
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate MEMO1 in samples. An antibody specific for MEMO1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyMEMO1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for MEMO1 is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of MEMO1 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview :
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : Q2HJ21
Abbreviation : MDM4
Alternative Names : RP11-430C7.1; DKFZp781B1423; HDMX; MDMX; MGC132766; MRP1; MDM4-related protein 1|Mdm4; transformed 3T3 cell double minute 4; p53 binding protein|double minute 4; human homolog of; p53-binding protei
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?6.2%
Inter-AssayCV : ?10.5%
Recovery : 1.12
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate MDM4 in samples. An antibody specific for MDM4 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyMDM4 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for MDM4 is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of MDM4 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview :
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : Q58DE2
Abbreviation : MRO
Alternative Names : B29; C18orf3; FLJ30140; OTTHUMP00000163544|beside the Ma29 deletion
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?4.7%
Inter-AssayCV : ?7.9%
Recovery : 1.04
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate MRO in samples. An antibody specific for MRO has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyMRO present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for MRO is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of MRO bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview :
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : Q32KV2
Abbreviation : MAEL
Alternative Names : FLJ14904; RP11-102C16.1; maelstrom homolog
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?6.5%
Inter-AssayCV : ?8.6%
Recovery : 0.99
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate MAEL in samples. An antibody specific for MAEL has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyMAEL present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for MAEL is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of MAEL bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : By excision of a P element insertion in the 5-prime UTR of the Drosophila maelstrom gene, Findley et al. (2003) isolated mael(M391), a n µLl allele of Drosophila maelstrom. They used database analysis to identify the human MAEL homolog. Confocal microscopy localized Drosophila maelstrom primarily to nuage, highly abundant particles within germline cells, and also to the nucleus and cytoplasm of germline cells. Nuclear shuttling assays showed that Drosophila maelstrom is transported between the cytoplasm and nucleus.By phenotypic characterization of Drosophila maelstrom mutants, which displayed axial patterning defects and other polarity defects, Findley et al. (2006) defined maelstrom as a spindle-class gene that affects Vasa modification.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : Q0IIL4
Abbreviation : TMEM167B
Alternative Names : AD-020; C1orf119; FLJ90710; protein x 013
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?4.1%
Inter-AssayCV : ?7.9%
Recovery : 0.96
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate TMEM167B in samples. An antibody specific for TMEM167B has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyTMEM167B present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for TMEM167B is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of TMEM167B bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : TMEM167B Belongs to the KISH family.A transmembrane protein (TP) protein that goes from one side of a membrane thro µgh to the other side of the membrane. Many TPs function as gateways or "loading docks" to deny or permit the transport of specific substances across the biological membrane, to get into the cell, or out of the cell as in the case of waste byproducts. As a response to the shape of certain molec µLes these "freight handling" TPs may have special ways of folding up or bending that will move a substance thro µgh the biological membrane. A transmembrane protein is a polytopic protein that spans an entire biological membrane. Transmembrane proteins aggregate and precipitate in water. They require detergents or nonpolar solvents for extraction, altho µgh some of them (beta-barrels) can be also extracted using denaturing agents.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Volume : 96 Tests. Other Volumes are also available. Please Inquire.
Research topic : Cancer
Uniprot ID : P05307
Species : Bovine
Former Code :
Alias : DSI, ERBA2L, GIT, P4Hbeta, PDI, PDIA1 PHDB, PO4DB, PO4HB, PROHB, collagen prolyl 4-hydroxylase beta|glutathione-ins µLin transhydrogenase|procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4
Product Type : ELISA Kit
Sample Type :
Detect Range : Request Information
Sensitivity : Request Information
Antigen Name : prolyl 4-hydroxylase, beta polypeptide
Abbreviation : P4HB
Protein Biological Process 1 :
Protein Biological Process 2 :
Protein Biological Process 3 :
Assay Time : 1-5h
Sample Volume : 50-100 µL
Detection Wavelength : 450 nm
Delievery Date : 7-14 working days

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : A4FV93
Abbreviation : DLK2
Alternative Names : EGFL9; MGC111055; MGC2487; EGF-like-domain; m µLtiple 9
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?3.8%
Inter-AssayCV : ?6.5%
Recovery : 1.01
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate DLK2 in samples. An antibody specific for DLK2 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyDLK2 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for DLK2 is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of DLK2 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : The Dlk1 gene appears to function as a reg µLator of adipogenesis. Ad µLt Dlk1-deficient mice are obese, but adipose tissue still develops in transgenic mice overexpressing an Fc-dlk1 fusion protein, and neither type of genetically modified mice displays serious abnormalities. EGFL9, encoding for a protein whose structural features are virtually identical to those of dlk1 s µggesting it may function in a similar way. As dlk1 does, the protein encoded by EGFL9/Dlk2 affects adipogenesis of 3T3-L1 preadipocytes and mesenchymal C3H10T1/2 cells; however, it does so in an opposite way to that of dlk1. In addition, expression levels of both genes appear to be inversely correlated in both cell lines. Moreover, enforced changes in the expression of one gene affect the expression levels of the other.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : P19782
Abbreviation : PRM2
Alternative Names : CT94.2; FLJ27447; Sperm protamine P2|cancer/testis antigen family 94; member 2
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?6.9%
Inter-AssayCV : ?10.9%
Recovery : 1.04
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate PRM2 in samples. An antibody specific for PRM2 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPRM2 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PRM2 is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of PRM2 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : Presumably PRM2 is located on human chromosome 16, close to PRM1 : in the mouse the corresponding 2 loci are closely linked, and in the Chinese hamster, probes specific for the 2 protamines hybridize to the same restriction fragments after digestion of hamster genomic DNA with any of 5 different restriction endonucleases (Reeves et al., 1987, 1989). The tight linkage may be of functional significance since PRM1 and PRM2 are among the limited number of genes known to be expressed postmeiotically in haploid cells. In mouse, only one P2 protamine has been detected, whereas in man, the P2 protamine family is represented by 3 protamines, HP2, HP3 and HP4, whose amino acid sequences are identical except at their amino terminal ends .
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : A4IFC9
Abbreviation : PTOV1
Alternative Names : ACID2; DKFZp586I111; MGC71475; prostate tumor overexpressed gene 1
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?5.1%
Inter-AssayCV : ?8.2%
Recovery : 0.97
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate PTOV1 in samples. An antibody specific for PTOV1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPTOV1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PTOV1 is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of PTOV1 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : PTOV1 was predicted to form alternating alpha helices and beta sheets. Normal prostate expressed low PTOV1 levels. Western blot analysis of prostate tumor tissue detected PTOV1 at an apparent molec µLar mass of 58 kD. Immunocytochemical analysis detected endogenous PTOV1 in the cytoplasm, concentrated around the nucleus.PTOV1 was overexpressed in 71% of 38 prostate carcinomas and in 80% of samples with prostate intraepithelial neoplasia. High levels of PTOV1 in tumors correlated significantly with proliferative index and localization of PTOV1 in the nucleus. In quiescent c µLtured prostate tumor cells, PTOV1 localized to the cytoplasm and was excluded from nuclei. After serum stim µLation, PTOV1 partially translocated to the nucleus at the beginning of S phase.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Volume : 96 Tests. Other Volumes are also available. Please Inquire.
Research topic : Metabolism
Uniprot ID : O02853
Species : Bovine
Former Code :
Alias : RP11-229P13.6, L-PGDS, LPGDS, PDS, PGD2, PGDS, PGDS2, PGD2 synthase|beta-trace protein|glutathione-independent PGD synthase|lipocalin-type prostaglandin D synthase|prostaglandin D synthase|prostagla
Product Type : ELISA Kit
Sample Type : serum, plasma, tissue homogenates
Detect Range : 93.75 pg/ml-6000 pg/ml
Sensitivity : 46.8pg/ml.
Antigen Name : prostaglandin D2 synthase 21kDa (brain)
Abbreviation : PTGDS
Protein Biological Process 1 : Biosynthesis/Metabolism
Protein Biological Process 2 : Lipogenesis and lipometabolism
Protein Biological Process 3 : Fatty acid biosynthesis
Assay Time : 1-5h
Sample Volume : 50-100 µL
Detection Wavelength : 450 nm
Delievery Date : 5-7 working days

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : O02853
Abbreviation : PTGDS
Alternative Names : RP11-229P13.6; L-PGDS; LPGDS; PDS; PGD2; PGDS; PGDS2; PGD2 synthase|beta-trace protein|glutathione-independent PGD synthase|lipocalin-type prostaglandin D synthase|prostaglandin D synthase|prostagla
Application : ELISA
Range : 93.75-6000 pg/mL
Sensitivity : 46.8 pg/mL
Intra-AssayCV : ?4.8%
Inter-AssayCV : ?10.2%
Recovery : 1.03
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate PTGDS in samples. An antibody specific for PTGDS has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPTGDS present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PTGDS is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of PTGDS bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : Prostaglandin D synthase catalyzes the conversion of prostaglandin H2 (PGH2) to postaglandin D2 (PGD2). Prostaglandin D synthase induces sleep, reg µLates nociception, inhibits platelet aggregation, and acts as an allergic mediator. Two distinct types of PGD synthase have been identified, namely the lipocalin type enzyme (b-trace) and the hematopoietic enzyme. Lipocalin type prostaglandin D synthase is localized in the central nervous system and male genital organs of various mammals and the human heart. This enzyme has been identified as b-trace, which is a major protein in human cerebrospinal fluid. Hematopoietic prostaglandin D synthase is widely distributed in the peripheral tissues and is localized in the antigen-presenting cells, mast cells, and megakaryocytes.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : Q32L99
Abbreviation : PTGR2
Alternative Names : DKFZp686P10120; FLJ39091; FLJ99229; PGR2; ZADH1; 15-oxoprostaglandin-delta13-reductase|zinc binding alcohol dehydrogenase; domain containing 1
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?6.9%
Inter-AssayCV : ?8.9%
Recovery : 1.03
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate PTGR2 in samples. An antibody specific for PTGR2 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPTGR2 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PTGR2 is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of PTGR2 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : PTGR2 is an enzyme involved in the metabolism of prostaglandins. The encoded protein catalyzes the NADPH-dependent conversion of 15-keto-prostaglandin E2 to 15-keto-13,14-dihydro-prostaglandin E2. This protein may also be involved in reg µLating activation of the peroxisome proliferator-activated receptor. Alternative splicing res µLts in m µLtiple transcript variants. ZADH1 has a domain characteristic of the zinc-containing ADH family , a proline-rich motif, and a putative NADP(+)-binding domain. RT-PCR detected ubiquitous expression of the shorter ZADH1 transcript (ZADH1b), with highest expression in kidney, liver, pancreas, prostate, and heart, followed by lung, skeletal muscle, testis, small intestine, and brain. Expression was low in all other tissues examined.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : Q3SZJ4
Abbreviation : PTGR1
Alternative Names : RP11-16L21.1; FLJ99229; LTB4DH; MGC34943; PGR1; ZADH3; 15-oxoprostaglandin 13-reductase|NADP-dependent leukotriene B4 12-hydroxydehydrogenase|leukotriene B4 12-hydroxydehydrogenase|zinc binding alco
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?5.3%
Inter-AssayCV : ?9.5%
Recovery : 0.97
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate PTGR1 in samples. An antibody specific for PTGR1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPTGR1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PTGR1 is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of PTGR1 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : PTGR1 isan enzyme that is involved in the inactivation of the chemotactic factor, leukotriene B4. The encoded protein specifically catalyzes the NADP+ dependent conversion of leukotriene B4 to 12-oxo-leukotriene B4. A pseudogene of this gene is found on chromosome 1. Alternative splicing res µLts in m µLtiple transcript variants. Leukotriene B(4) 12-hydroxydehydrogenase catalyzes the conversion of leukotriene B(4) into 12-oxo-leukotriene B(4), its less-active metabolite.The identity between the porcine and human sequences they obtained is 83.5% at the amino acid level and 84.7% at the nucleotide level. Both enzymes are highly homologous with a protein, AdRab-F, expressed only in ad µLt rabbit small intestine
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : O62664
Abbreviation : PTGS1
Alternative Names : RP11-542K23.6; COX1; COX3; PCOX1; PGG/HS; PGHS-1; PGHS1; PHS1; PTGHS; prostaglandin G/H synthase and cyclooxygenase|prostaglandin-endoperoxide synthase 1
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?6.3%
Inter-AssayCV : ?10.6%
Recovery : 1.06
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate PTGS1 in samples. An antibody specific for PTGS1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPTGS1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PTGS1 is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of PTGS1 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : There are two isozymes of PTGS : a constitutive PTGS1 and an inducible PTGS2, which differ in their reg µLation of expression and tissue distribution. PTGS1 which reg µLates angiogenesis in endothelial cells, and is inhibited by nonsteroidal anti-inflammatory dr µgs such as aspirin. Recent research has shown that the inhibition of COX-1 is the main reason why aspirin is effective at reducing cardiac events (as opposed to aspirin's anti-platelet aggregation effects). PTGS1 is tho µght to be involved in cell-cell signaling and maintaining tissue homeostasis. Alternative splicing of this gene generates two transcript variants called COX-1 and COX-3. The expression of these two transcripts is differentially reg µLated by relevant cytokines and growth factors.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : N/A
Abbreviation : PGF2a
Alternative Names : PGF2A; PGF2-A; PG-F2a
Application : ELISA
Range : 9.88-800 pg/mL
Sensitivity : 3.88 pg/mL
Intra-AssayCV : ?4.7%
Inter-AssayCV : ?7.3%
Recovery : 0.98
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate PGF2a in samples. An antibody specific for PGF2a has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPGF2a present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PGF2a is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of PGF2a bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : One of the prostaglandins, a group of hormone-like substances that participate in a wide range of body functions such as the contraction and relaxation of smooth muscle, the dilation and constriction of blood vessels, control of blood pressure, and mod µLation of inflammation. Prostaglandin F2-alpha(PGF-2 alpha) is a stable prostaglandin that stim µLates the contraction of uterine and bronchial smooth muscle and produces vasoconstriction (tightening) in some blood vessels. As a pharmaceutical, the generic name of PGF-2 alpha is dinoprost. It is used for the induction of abortion, for evacuation of the uterus after a missed abortion, and in the treatment of hydatidiform mole.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : Q29626
Abbreviation : PTGIS
Alternative Names : CYP8; CYP8A1; MGC126858; MGC126860; PGIS; PTGI; cytochrome P450; family 8; subfamily A; polypeptide 1|prostaglandin I2 synthase
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?5.1%
Inter-AssayCV : ?10.5%
Recovery : 1.06
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate PTGIS in samples. An antibody specific for PTGIS has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPTGIS present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PTGIS is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of PTGIS bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : Prostaglandin I2 (prostacyclin) synthase is a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in dr µg metabolism and synthesis of cholesterol, steroids and other lipids. However, this protein is considered a member of the cytochrome P450 superfamily on the basis of sequence similarity rather than functional similarity. This endoplasmic retic µLum membrane protein catalyzes the conversion of prostaglandin H2 to prostacyclin (prostaglandin I2), a potent vasodilator and inhibitor of platelet aggregation. An imbalance of prostacyclin and its physiological antagonist thromboxane A2 contribute to the development of myocardial infarction, stroke, and atherosclerosis.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : P79393
Abbreviation : PTGIR
Alternative Names : IP; MGC102830; PRIPR; PGI receptor|prostacyclin receptor|prostanoid IP receptor
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?5.6%
Inter-AssayCV : ?10.3%
Recovery : 1.02
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate PTGIR in samples. An antibody specific for PTGIR has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPTGIR present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PTGIR is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of PTGIR bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : Prostacyclin receptor is a member of the G-protein coupled receptor family. Prostacyclin, the major product of cyclooxygenase in macrovasc µLar endothelium, elicits a potent vasodilation and inhibition of platelet aggregation thro µgh binding to this receptor. When binding a prostacyclin-molec µLe, the receptor changes conformation and activates Gs, with its activation of cAMP and increase in protein kinase A (PKA) activity.In vasodilation, the PKA activity causes phosphorylation of MLCK, decreasing its activity, res µLting in dephosphorylation of MLC of myosin. The smooth muscle relaxation leads to vasodilation.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Volume : 96-test Kit. Other Volumes are also available. Please contact us.
Assay Type :
Detection Range :
Sensitivity :
Species : Bovine
GeneName : PROS1
Alternative Names : PROS
Uniport : P07224

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : Q9XTA2
Abbreviation : PREP
Alternative Names : RP3-355L5.1; MGC16060; PE; PEP; dJ355L5.1 (prolyl endopeptidase)|post-proline cleaving enzyme|prolyl oligopeptidase
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?6.8%
Inter-AssayCV : ?10.8%
Recovery : 1.08
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate PREP in samples. An antibody specific for PREP has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPREP present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PREP is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of PREP bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : Prolyl endopeptidase (PE) also known as prolyl oligopeptidase or post-proline cleaving enzyme is an enzyme that in humans is encoded by the PREP gene.Prolyl endopeptidase is a large cytosolic enzyme that belongs to a distinct class of serine peptidases. It was first described in the cytosol of rabbit brain as an oligopeptidase, which degrades the nonapeptide bradykinin at the Pro-Phe bond.[5] The enzyme is involved in the maturation and degradation of peptide hormones and neuropeptides such as alpha-melanocyte-stim µLating hormone, luteinizing hormone-releasing hormone (LH-RH), thyrotropin-releasing hormone, angiotensin, neurotensin, oxytocin, substance P and vasopressin. PREP cleaves peptide bonds at the C-terminal side of proline residues. Its activity is confined to action on oligopeptides of less than 10 kD and it has an absolute requirement for the trans-configuration of the peptide bond preceding proline. Prolyl endopeptidases are involved in the maturation and degradation of peptide hormones and neuropeptides.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : Q148G5
Abbreviation : PRODH
Alternative Names : FLJ33744; HSPOX2; MGC148078; MGC148079; PIG6; POX; PRODH1; PRODH2; SCZD4; TP53I6; proline dehydrogenase 1|proline oxidase 2|proline oxidase; mitochondrial|tumor protein p53 inducible protein 6
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?5.2%
Inter-AssayCV : ?7.8%
Recovery : 0.9
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate PRODH in samples. An antibody specific for PRODH has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPRODH present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PRODH is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of PRODH bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview :
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).