CYP11B1/2 rabbit pAb

CYP11B1/2 rabbit pAb

AO-06-ES3954-100

CYP11B1/2 rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES3954
Product nameCYP11B1/2 rabbit pAb
ReactivityHuman
ApplicationsWB;ELISA
Other nameCYP11B1; S11BH; Cytochrome P450 11B1, mitochondrial; CYPXIB1; Cytochrome P-450c11; Cytochrome P450C11; Steroid 11-beta-hydroxylase; CYP11B2;Cytochrome P450 11B2, mitochondrial; Aldosterone synthase; ALDOS; Aldosterone-synthesizing enzyme; CYPXIB2; Cytochrome P-450Aldo; Cytochrome P-450C18; Steroid 18-hydroxylase
Size100μL
Unit price ($)248
Human gene ID1584
Human Swiss-ProtP15538
SourceRabbit
IsotypeIgG
TargetCYP11B1/2
Fields>>Steroid hormone biosynthesis;>>Metabolic pathways;>>Cortisol synthesis and secretion;>>Cushing syndrome
Gene nameCYP11B1/CYP11B2
Protein nameCytochrome P450 11B1 mitochondrial/Cytochrome P450 11B2 mitochondrial
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID
Mouse gene link
Mouse Swiss-Prot
Mouse Swiss link
Rat gene ID
Rat gene link
Rat Swiss-Prot
Rat Swiss link
ImmunogenThe antiserum was produced against synthesized peptide derived from the N-terminal region of human CYP11B1/2. AA range:61-110
SpecificityCYP11B1/2 Polyclonal Antibody detects endogenous levels of CYP11B1/2 protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. ELISA: 1/20000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)58kD
Backgroundcytochrome P450 family 11 subfamily B member 1(CYP11B1) Homo sapiens 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 protein localizes to the mitochondrial inner membrane and is involved in the conversion of progesterone to cortisol in the adrenal cortex. Mutations in this gene cause congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency. Transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Jul 2008],
Functioncatalytic activity:A steroid + reduced adrenal ferredoxin + O(2) = an 11-beta-hydroxysteroid + oxidized adrenal ferredoxin + H(2)O.,cofactor:Heme group.,disease:An anti-Lepore-type fusion of the CYP11B1 and CYP11B2 genes is a cause of glucocorticoid-remediable aldosteronism (GRA) [MIM:103900].,disease:Defects in CYP11B1 are the cause of adrenal hyperplasia type 4 (AH4) [MIM:202010]. AH4 is a form of congenital adrenal hyperplasia, a common recessive disease due to defective synthesis of cortisol. Congenital adrenal hyperplasia is characterized by androgen excess leading to ambiguous genitalia in affected females, rapid somatic growth during childhood in both sexes with premature closure of the epiphyses and short adult stature. Four clinical types: "salt wasting" (SW, the most severe type), "simple virilizing" (SV, less severely affected patients), with normal aldosterone biosynthesis, "
Subcellular locationMitochondrion inner membrane ; Peripheral membrane protein .
ExpressionAdrenal gland,PCR rescued clones,Peripheral blood,

Additional Images

Image 1
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Western Blot analysis of HT29, HuvEc, K562 cells using CYP11B1/2 Polyclonal Antibody. Secondary antibody(catalog#:RS0002) was diluted at 1:20000
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Western blot analysis of lysate from HT29 cells, using CYP11B1/2 Antibody.
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: AO-06-ES3954-100
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