CYP7B1 Rabbit Polyclonal Antibody
Other products for "CYP7B1"
Specifications
Product Data | |
Applications | IHC, WB |
Recommended Dilution | Western Blot: 1/500-1/1000. Immunohistochemistry on Paraffin Sections: 1/50-1/200. |
Reactivities | Human |
Host | Rabbit |
Clonality | Polyclonal |
Specificity | This antibody detects endogenous levels of CYP7B1 protein. (region surrounding Gln127) |
Formulation | PBS pH~7.2 with 0.05% Sodium Azide as preservative State: Aff - Purified State: Liquid purified Ig fraction (>95% pure by SDS-PAGE) |
Concentration | 1.0 mg/ml |
Purification | Affinity-Chromatography using epitope-specific immunogen |
Predicted Protein Size | ~ 58 kDa |
Gene Name | Homo sapiens cytochrome P450 family 7 subfamily B member 1 (CYP7B1), transcript variant 1 |
Database Link | |
Background | P450 enzymes constitute a family of monooxygenase enzymes that are involved in the metabolism of a wide array of endogenous and xenobiotic compounds including cholesterol. CYP8B1 moderates the ratio of cholic acid over chenodeoxycholic acid to control the solubility of cholesterol. P450 cholesterol 7-hydroxylase, CYP7A1, is the rate limiting enzyme of bile acid synthesis in the liver, and its expression is mediated by the bile acid receptor FXR. CYP27A1 catalyzes vitamin D3 25-hydroxylation and is localized to the mitochondria in kidney and liver. CYP7B1 (oxysterol 7-α-hydroxylase) functions as an enzyme in the alternate bile acid synthesis pathway. Specifically, CYP7B1 metabolizes 25-and 27-hydroxycholesterol. The gene encoding human CYP7B1 maps to chromosome 8q21.3. Mutations in the CYP7B1 gene may cause a metabolic defect in bile acid synthesis characterized by elevated urinary bile acid excretion, severe cholestasis, cirrhosis and liver synthetic failure. |
Synonyms | Cytochrome P450 7B1 |
Reference Data | |
Protein Families | Druggable Genome, P450, Transmembrane |
Protein Pathways | Primary bile acid biosynthesis |
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