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Browse our anti-CYP11B1 (CYP11B1) Antibodies

Full name:
anti-Cytochrome P450, Family 11, Subfamily B, Polypeptide 1 Antibodies (CYP11B1)
On are 47 Cytochrome P450, Family 11, Subfamily B, Polypeptide 1 (CYP11B1) Antibodies from 13 different suppliers available. Additionally we are shipping CYP11B1 Kits (10) and CYP11B1 Proteins (9) and many more products for this protein. A total of 74 CYP11B1 products are currently listed.
AA389061, Cp11ba, CPN1, Cyp11b, Cyp11b-1, FHI, P450c11, RATCP11BA
list all antibodies Gene Name GeneID UniProt
CYP11B1 1584 P15538
CYP11B1 110115  
CYP11B1 500892  

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anti-Human CYP11B1 Antibodies:

anti-Mouse (Murine) CYP11B1 Antibodies:

anti-Rat (Rattus) CYP11B1 Antibodies:

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Top referenced anti-CYP11B1 Antibodies

  1. Human Polyclonal CYP11B1 Primary Antibody for WB - ABIN611372 : Hassett, Aicher, Sidhu, Omiecinski: Human microsomal epoxide hydrolase: genetic polymorphism and functional expression in vitro of amino acid variants. in Human molecular genetics 1994 (PubMed)
    Show all 3 references for ABIN611372

More Antibodies against CYP11B1 Interaction Partners

Human Cytochrome P450, Family 11, Subfamily B, Polypeptide 1 (CYP11B1) interaction partners

  1. Data from a 19-year-old Chinese woman and her parents suggest congenital adrenal hyperplasia due to steroid 11beta-hydroxylase deficiency can be attributed to both a novel deletion mutation (g.9525_9526delCT, corresponding to p.L380V em leaderR420X) and a known missense mutation (g.5194G>C corresponding to p.D63H) in CYP11B1. [CASE-REPORT]

  2. Congenital adrenal hyperplasia caused by novel mutations in the CYP11B1 gene.

  3. Chimeric CYP11B2 (show CYP11B2 Antibodies)/CYP11B1 causing 11beta-hydroxylase deficiency in Chinese patients with congenital adrenal hyperplasia

  4. Seven novel CYP11B1 mutations identified in Chinese patients with 11 beta-hydroxylase deficiency.

  5. Mutations in the CYP11B1 gene are the cause of 11beta-hydroxylase deficiency.

  6. study of the functional consequences of 3 novel and 1 previously described CYP11B1 gene mutations (p.(Arg143Trp), p.(Ala306Val), p.(Glu310Lys) and p.(Arg332Gln)) detected in patients suffering from classical and non-classical 11beta-OHD

  7. Heterogenous immunolocalization of CYP11B2 (show CYP11B2 Antibodies) and diffuse immunoreactivity of CYP11B1 were detected.

  8. Data from recombinant proteins suggest three additional mutations in CYP11B1 (p.His125Thrfs*8; p.Leu463_Leu464dup; p.Ser150Leu) can account for congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency (classical/non-classical phenotype).

  9. Analysis of the CYP11B1 gene revealed two novel mutations, a small insertion in exon 7 (InsAG393) and a small deletion in exon 2 (DelG766), and three previously known missense mutations (T318M, Q356X, and R427H).

  10. Expression of P45011beta and StAR (steroidogenic acute regulatory protein (show STAR Antibodies)) is down-regulated in adrenocortical cells and neurons under oxidative stress by ALADIN (show AAAS Antibodies) (triple A syndrome protein, human) knockdown.

Mouse (Murine) Cytochrome P450, Family 11, Subfamily B, Polypeptide 1 (CYP11B1) interaction partners

  1. Cyp11b1 is induced in the murine gonad by luteinizing hormone/human chorionic gonadotropin and involved in the production of 11-ketotestosterone, a major fish androgen.

  2. 3-methylsulfonyl-DDE and related compounds did not alter Cyp11b1 gene expression in adrenocortical Y-1 cells indicating that compound-induced enzyme inhibition occurs on the protein level.

  3. These data showed that in the adrenal gland, PREB (show PREB Antibodies) regulates the transcription of the CYP11B1 gene via cAMP.

  4. Cyp11b1 null mouse, a model of congenital adrenal hyperplasia

Cow (Bovine) Cytochrome P450, Family 11, Subfamily B, Polypeptide 1 (CYP11B1) interaction partners

  1. A simultaneous analysis of the influence of CYP11B1 and DGAT1 (show DGAT1 Antibodies) on multiple variables of a German Holstein pedigree is presented.

CYP11B1 Antigen Profile

Antigen Summary

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.

Alternative names and synonyms associated with CYP11B1

  • cytochrome P450, family 11, subfamily B, polypeptide 1 (CYP11B1) antibody
  • cytochrome P450, family 11, subfamily b, polypeptide 1 (Cyp11b1) antibody
  • cytochrome P450, subfamily XI B, polypeptide 1 (CYP11B1) antibody
  • AA389061 antibody
  • Cp11ba antibody
  • CPN1 antibody
  • Cyp11b antibody
  • Cyp11b-1 antibody
  • FHI antibody
  • P450c11 antibody
  • RATCP11BA antibody

Protein level used designations for CYP11B1

cytochrome P450 11B1, mitochondrial , CYPXIB1 , cytochrome P-450c11 , cytochrome P450, subfamily XIB (steroid 11-beta-hydroxylase), polypeptide 1 , cytochrome P450C11 , cytochrome p450 XIB1 , steroid 11-beta-hydroxylase , steroid 11-beta-monooxygenase , steroid-11-beta-hydroxylase , Cytochrome P450, subfamily XIB, polypeptide 1 (steroid 11-beta-hydroxylase) , P450(11 beta)-DS , P450C11 , aldosterone synthase , cytochrome P450(11 beta)-DS , cytochrome P450, subfamily 11B, polypeptide 1 , 11-beta-hydroxylase , 11beta-hydroxylase

695793 Macaca mulatta
1584 Homo sapiens
110115 Mus musculus
500892 Rattus norvegicus
100135511 Cavia porcellus
767576 Ovis aries
282422 Bos taurus
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