Product Name
CYP11B1, Polyclonal Antibody
Full Product Name
CYP11B1 Polyclonal Antibody
Product Synonym Names
CPN1; CYP11B; FHI; P450C11
Product Gene Name
anti-CYP11B1 antibody
[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Immunogen Sequence
TVQLMFMPRS LSRWTSPKVW KEHFEAWDCI FQYGDNCIQK IYQELAFSRP QQYTSIVAEL LLNAELSPDA IKANSMELTA GSVDTTVFPL LMTLFELARN PNVQQALRQE SLAAAASISE HPQKATTELP LLRAALKETL RLYPVGLFLE RVASSDLVLQ NYHIPAGTLV RVFLYSLGRN PALFPRPERY NPQRWLDIRG SGRNFYHVPF GFGMRQCLGR RLAEAEMLLL LHHVLKHLQV ETLTQEDIKM VYSFI
3D Structure
ModBase 3D Structure for P15538
Purity/Purification
Affinity Purification
Immunogen
Recombinant protein of human CYP11B1
Storage Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Cellular Location
Mitochondrion membrane
Preparation and Storage
Store at -20 degree C. Avoid freeze / thaw cycles.
Other Notes
Small volumes of anti-CYP11B1 antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Related Product Information for
anti-CYP11B1 antibody
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.
Product Categories/Family for anti-CYP11B1 antibody
Polyclonal Antibodies
Applications Tested/Suitable for anti-CYP11B1 antibody
Immunofluorescence (IF)
Application Notes for anti-CYP11B1 antibody
IF: 1:50 - 1:200
NCBI/Uniprot data below describe general gene information for CYP11B1. It may not necessarily be applicable to this product.
NCBI Accession #
NP_000488.3
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NCBI GenBank Nucleotide #
NM_000497.3
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UniProt Primary Accession #
P15538
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UniProt Secondary Accession #
Q14095; Q4VAQ8; Q4VAQ9; Q9UML2[Other Products]
UniProt Related Accession #
P15538[Other Products]
Molecular Weight
49kDa/57kDa
NCBI Official Full Name
cytochrome P450 11B1, mitochondrial isoform 1
NCBI Official Synonym Full Names
cytochrome P450 family 11 subfamily B member 1
NCBI Official Symbol
CYP11B1 [Similar Products]
NCBI Official Synonym Symbols
FHI; CPN1; CYP11B; P450C11
[Similar Products]
NCBI Protein Information
cytochrome P450 11B1, mitochondrial
UniProt Protein Name
Cytochrome P450 11B1, mitochondrial
UniProt Synonym Protein Names
CYPXIB1; Cytochrome P-450c11; Cytochrome P450C11; Steroid 11-beta-hydroxylase (EC:1.14.15.4)
Protein Family
Cytochrome
UniProt Gene Name
CYP11B1 [Similar Products]
UniProt Synonym Gene Names
S11BH; Cytochrome P450C11 [Similar Products]
NCBI Summary for CYP11B1
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]
UniProt Comments for CYP11B1
Has steroid 11-beta-hydroxylase activity. In addition to this activity, the 18 or 19-hydroxylation of steroids and the aromatization of androstendione to estrone have also been ascribed to cytochrome P450 XIB.
Research Articles on CYP11B1
1. We conclude that 11 beta-OHD in Saudi Arabia has a unique genotype with a high rate of novel mutations. The novel p. R448P mutation is the most common mutation in this highly inbred population.
Precautions
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Disclaimer
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