CYB5R3 (C-term) Goat Polyclonal Antibody
CAT#: AP23662PU-N
CYB5R3 (C-term) goat polyclonal antibody, Aff - Purified
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CNY 5,371.00
货期*
4周
规格
Specifications
Product Data | |
Applications | ELISA, IHC, WB |
Recommend 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. |
Reactivity | 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. |
Conjugation | Unconjugated |
Storage Condition | Store undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer. Avoid repeated freezing and thawing. |
Gene Name | cytochrome b5 reductase 3 |
Database Link | |
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 |
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