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HCCS rabbit pAb - 100 μL

HCCS rabbit pAb - 100 μL

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HoloCytochrome c synthase (HCCS) Homo sapiens The protein encoded by this gene is an enzyme that covalently links a heme group to the apoprotein of Cytochrome c. Defects in this gene are a cause of microphthalmia syndromic type 7 (MCOPS7). Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jan 2010],

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HCCS rabbit pAb
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