HCCS Polyclonal Antibody

Background:
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],

Alternative Names:
HCCS, CCHL, Cytochrome c-type heme lyase, CCHL, Holocytochrome c-type synthase

Immunogen: The antiserum was produced against synthesized peptide derived from human Cytochrome c-type Heme Lyase. AA range:81-130

Isotype: Rabbit

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Concentration: 1 mg/ml

Observed band: 31

GeneID: HCCS

Storage: -20°C/1 year

NOTE: For Research Use Only