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HCCS
Holocytochrome c synthaseCCHL, MLS
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]
Top validated antibodies |
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| Proteintech Group |  15118-1-AP |
3 references | Polyclonal |
WB
EL
ICC
IP
IHC
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| Invitrogen Antibodies | 15118-1-AP |
Polyclonal |
WB
ICC
IP
IHC
OA
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| NSJ Bioreagents | RQ6486 |
Polyclonal |
WB
EL
ICC
IHC
FC
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| Atlas Antibodies | HPA002946 |
1 references | Polyclonal |
WB
ICC
IHC
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| Novus Biologicals | NBP1-86577 |
1 references | Polyclonal |
WB
ICC
IHC
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