Cytochrome b5 Polyclonal Antibody

Background:
cytochrome b5 type A(CYB5A) Homo sapiens The protein encoded by this gene is a membrane-bound cytochrome that reduces ferric hemoglobin (methemoglobin) to ferrous hemoglobin, which is required for stearyl-CoA-desaturase activity. Defects in this gene are a cause of type IV hereditary methemoglobinemia. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2010],

Alternative Names:
CYB5A, CYB5, Cytochrome b5, Microsomal cytochrome b5 type A, MCB5

Immunogen: The antiserum was produced against synthesized peptide derived from human CYB5. AA range:61-110

Isotype: Rabbit

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

Concentration: 1 mg/ml

Observed band: 15

GeneID: CYB5A

Storage: -20°C/1 year

NOTE: For Research Use Only