
Supplier:
Boster ImmunoleaderCat no: PA1699
Polyclonal Anti-CYP11B1
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SPECIFICATIONS
Price
200.00 USD
Catalog Number
PA1699
Size
100ug/vial
Applications
WB
Reactivities
Hum
Form
Lyophilized
Format
Each vial contains 5mg BSA, 0.9mg NaCl, 0.2mg Na2HPO4, 0.05mg Thimerosal, 0.05mg NaN3.
Gene Id
CYP11B1
References
1.Chua, S. C., Szabo, P., Vitek, A., Grzeschik, K.-H., John, M., White, P. C. Cloning of cDNA encoding steroid 11-beta-hydroxylase (P450C11). Proc. Nat. Acad. Sci. 84: 7193-7197, 1987. \n2.Cicila, G. T., Rapp, J. P., Wang, J. M., St. Lezin, E., Ng, S. C., Kurtz, T. W. Linkage of 11-beta-hydroxylase mutations with altered steroid biosynthesis and blood pressure in the Dahl rat. Nature Genet. 3: 346-353, 1993.\n3.Ezquieta, B., Luzuriaga, C. Neonatal salt-wasting and 11 beta-hydroxylase deficiency in a child carrying a homozygous deletion hybrid CYP11B2 (aldosterone synthase)-CYP11B1 (11 beta-hydroxylase). Clin. Genet. 66: 229-235, 2004.\n
Swiss Prot
P15538
Storage Temp
At -20 degree C for one year. After reconstitution, at 4 degree C for one month. It can also be aliquotted and stored frozen at -20 degree C for a longer time.Avoid repeated freezing and thawing.
Additional Info
A synthetic peptide corresponding to a sequence at the C-terminal of human CYP11B1.
Scientific Background
CYP11B1 (Cytochrome p450, family 11, subfamily B, polypeptide 1), also called Steroid 11-beta-hydroxylase or P450C11, is a steroid hydroxylase found in the zona fasciculata. The CYP11B1 gene functions primarily in mitochondria in the zona fasciculata of the adrenal cortex to convert 11-deoxycortisol to cortisol and 11-deoxycorticosterone to corticosterone. CYP11B1 is a member of the cytochrome P450 superfamily of enzymes. It is mapped on 8q24.3. The CYP11B1 gene contains 9 exons and spans 6.5 kb. Using RT-PCR, Kayes-Wandover and White detected CYP11B1 mRNA in human cardiac tissue samples from left and right atria, aorta, apex, intraventricular septum, and atrioventricular node, as well as whole adult and fetal heart. Ventricles did not express CYP11B1. In patients with 11-beta-hydroxylase deficiency leading to hypertension and congenital adrenal hyperplasia, Pascoe et al. identified mutations in the CYP11B1 gene.\n\n
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