CYB5R3 (C-term) Goat Polyclonal Antibody

CAT#: AP23662PU-N

CYB5R3 (C-term) goat polyclonal antibody, Aff - Purified

Product Images

Cyb5r3 antibody staining of Human Umbilical Cord lysate at 0.01 ug/ml (35ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.

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  Cyb5r3 antibody staining of paraffin embedded Human Adrenal Gland at 3.8 ug/ml. Steamed antigen retrieval with citrate buffer pH 6, AP-staining.

Specifications

Product Data

• Applications: ELISA, IHC, WB
• Recommended Dilution: Peptide ELISA: 1/32000 (Detection Limit).
  Western Blot: 0.01-0.03 µg/ml. Approx 37kDa band observed in Human Placenta, Testis and Umbilical Cord lysates.
  Immunohistochemistry on Paraffin Sections: 3-5 µg/ml. In paraffin embedded Human Adrenal Gland shows heavy vesicular/granular staining in the cytoplasm of medular cells.
• Reactivities: Human
• Host: Goat
• Clonality: Polyclonal
• Immunogen: Synthetic peptide from the C-terminus of human CYB5R3 (NP_000389.1; NP_001123291.1; NP_001165131.1).
• Specificity: This antibody is expected to recognize all three reported isoforms (NP_000389.1, NP_001123291.1 and NP_001165131.1).
• Formulation: Tris saline, pH~7.3
  State: Aff - Purified
  State: Liquid purified IgG fraction.
  Stabilizer: 0.5% BSA
  Preservative: 0.02% Sodium Azide
• Concentration: lot specific
• Purification: Ammonium Sulphate Precipitation followed by antigen Affinity Chromatography using the immunizing peptide.
• Storage: Store undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer.
  Avoid repeated freezing and thawing.
• Stability: Shelf life: one year from despatch.
• Gene Name: Homo sapiens cytochrome b5 reductase 3 (CYB5R3), transcript variant 1
• Database Link:
  Entrez Gene 1727 Human
• Background: CYB5R3 belongs to the flavoprotein pyridine nucleotide cytochrome reductase family and contains 1 FAD-binding FR-type domain. There are two isoforms, NADH-cytochrome b5 reductase 3 membrane bound form and NADH-cytochrome b5 reductase 3 soluble form. Its functions include desaturation and elongation of fatty acids, cholesterol biosynthesis, drug metabolism, and, in erythrocyte, methemoglobin reduction. Defects in CYB5R3 are the cause of hereditary methemoglobinemia (HM). There are three forms of this disease: type 1 (HM1) in which the enzyme is only deficient in erythrocytes with a mild cyanosis; type 2 (HM2), in which the enzyme is completely deficient; type 3 (HM3) where the deficiency is seen in all blood cells. Type 2 is a severe form accompanied with mental retardation and neurological impairment.
• Synonyms: NADH-cytochrome b5 reductase 3, B5R, DIA1, Diaphorase-1
• Note: Calculated Molecular Weight: 38.2kDa (NP_001165131.1).

Reference Data

• Protein Families: Druggable Genome
• Protein Pathways: Amino sugar and nucleotide sugar metabolism