CYP27A1 Polyclonal Antibody
| 规格： | / 20μL / 60μL / 120μL / 200μL |
| 价格： | / ￥420 / ￥1010 / ￥1640 / ￥2365 |
货号：E-AB-11121
宿主: Rabbit
反应性: H
应用: IHC
Overview
| Synonyms | 12-alpha-triol 27-hydroxylase,5-beta-cholestane-3-alpha,5-beta-cholestane-3-alpha,7-alpha,12-alpha-triol 26-hydroxylase,5-beta-cholestane-3-alpha,7-alpha,12-alpha-triol 27-hydroxylase,5-beta-cholestane-3-alpha,7-alpha,12-alpha-triol 27-hydroxylase,7-alpha,Cholestanetriol 26 monooxygenase,CP27,CP27A,CTX,CYP,CYP27,CYP27A1,Cytochrome P 450C27/25,Cytochrome P-450C27/25,Cytochrome P450 27,Cytochrome P450 27 mitochondrial,Cytochrome P450 family 27 subfamily A member 1,Cytochrome P450 family 27 subfamily A polypeptide 1,Cytochrome P450 subfamily XXVIIA (steroid 27-hydroxylase cerebrotendinous xanthomatosis) polypeptide 1,mitochondrial,Sterol 26 hydroxylase,Sterol 26 hydroxylase mitochondrial,Sterol 26-hydroxylase,Sterol 27 hydroxylase,Sterol 27-hydroxylase,Vitamin D(3) 25 hydroxylase,Vitamin D(3) 25-hydroxylase,CYP27A1抗体 |
| Swissprot | Q02318 |
| Source | Rabbit |
| Reactivity | Human |
| Immunogen | Recombinant protein of human CYP27A1 |
| Application | IHC(Detection kit: E-IR-R213) |
| Recommended dilution | IHC,,1:50-1:200 |
| Concentration | 0.6 mg/mL |
| Clonality | Polyclonal |
Properties
| Cellular localization | Mitochondrion membrane. |
| Isotype | IgG |
| Purification | Affinity purification |
| Conjugation | Unconjugated |
| Storage instructions | Store at -20℃. Avoid freeze / thaw cycles. |
| Storage buffer | PBS with 0.05% sodium azide, 50% glycerol, PH7.3 |
| Background | This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This mitochondrial protein oxidizes cholesterol intermediates as part of the bile synthesis pathway. Since the conversion of cholesterol to bile acids is the major route for removing cholesterol from the body, this protein is important for overall cholesterol homeostasis. Mutations in this gene cause cerebrotendinous xanthomatosis, a rare autosomal recessive lipid storage disease. |
