Cytochrome b5 Polyclonal Antibody

Background:
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.

Research Area: Cancer, Metabolism, Signal Transduction

Synonyms:
CYB 5, CYB 5A, CYB5, CYB5, Cyb5a, Cytochrome b 5, Cytochrome b5 (microsomal), Cytochrome b5, Cytochrome b5 type A (microsomal), Cytochrome b5 type A, MCB 5, MCB5, Microsomal cytochrome b5, Microsomal cytochrome b5 type A, Type 1 cyt b5

Immunogen: Recombinant protein of human CYB5A

Swissprot: P00167
Gene Accession: NP_683725

Calculated MW: 15 kDa

Purification Method: Affinity purification

Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4

Concentration: 0.4 mg/mL
Dilution: WB 1:200-1:1000, IHC 1:50-1:200

Storage:
Store at -20°C. Avoid freeze / thaw cycles.

Alternative for product with catalog number:
sc-9513/sc-48470/sc-33174