AFG3L2 rabbit pAb - 50 μL
This gene encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders. [provided by RefSeq, Jul 2008],
Référence interne:
ES8866
URL de site web:
/shop/afg3l2-rabbit-pab-50-ml-655256
Distributed by Gentaur

View the Technical Datasheet of the product below

View the Technical Datasheet of the product below
Our latest content
Check out what's new in our company !
Your Dynamic Snippet will be displayed here... This message is displayed because you did not provide both a filter and a template to use.