Anti-CYB5R3 Antibody [JE63-51]
HA721008
ApplicationsWestern Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
TargetCYB5R3
Overview
- SupplierHUABIO
- Product NameAnti-CYB5R3 Antibody [JE63-51]
- Delivery Days Customer2
- ApplicationsWestern Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
- CertificationResearch Use Only
- ClonalityMonoclonal
- Clone IDJE63-51
- Concentration1 mg/ml
- ConjugateUnconjugated
- Gene ID1727
- Target nameCYB5R3
- Target descriptioncytochrome b5 reductase 3
- Target synonymsB5R, DIA1, NADH-cytochrome b5 reductase 3, NADH-cytochrome b5 reductase 3 membrane-bound form, NADH-cytochrome b5 reductase 3 soluble form, diaphorase-1, mutant NADH-cytochrome b5 reductase
- HostRabbit
- IsotypeIgG
- Protein IDP00387
- Protein NameNADH-cytochrome b5 reductase 3
- Scientific DescriptionNADH-cytochrome b5 reductase 3 is an enzyme that in humans is encoded by the CYB5R3 gene. Cytochrome b5 reductase is involved in the transfer of reducing equivalents from the physiological electron donor, NADH, via an FAD domain to the small molecules of cytochrome b5. Its also heavily involved in many oxidation and reduction reactions, such as the reduction of methemoglobin to hemoglobin.[8] Of the two forms of NADH-cytochrome b5 reductase, the membrane-bound form exists mainly on the cytoplasmic side of the endoplasmic reticulum and functions in desaturation and elongation of fatty acids, in cholesterol biosynthesis, and in drug metabolism. The erythrocyte form is located in a soluble fraction of circulating erythrocytes and is involved in methemoglobin reduction. Mutations in the CYB5R3 gene cause methemoglobinemia types I and II. This is a rare autosomal recessive disease due to a deficiency of isoform of NADH-cytochrome b5 reductase.
- Storage Instruction-20°C,2°C to 8°C
- UNSPSC41116161