Cytochrome P450 26B (CYP26B1) (NM_019885) Human Recombinant Protein
CAT#: TP762329
Purified recombinant protein of Human cytochrome P450, family 26, subfamily B, polypeptide 1 (CYP26B1), Pro229-End, with N-terminal His tag, expressed in E.coli, 50ug
Other products for "CYP26B1"
Specifications
Product Data | |
Species | Human |
Expression Host | E. coli |
Expression cDNA Clone or AA Sequence |
A DNA sequence encoding the region(Pro229-End) of CYP26B1
|
Tag | N-His |
Predicted MW | 31.8 kDa |
Concentration | >50 ug/mL as determined by microplate BCA method |
Purity | > 80% as determined by SDS-PAGE and Coomassie blue staining |
Buffer | 50mM Tris, pH8.0, 8M Urea |
Storage | Store at -80°C after receiving vials. |
Stability | Stable for at least 1 year from receipt of products under proper storage and handling conditions. Avoid repeated freeze-thaw cycles. |
Reference Data | |
RefSeq | NP_063938 |
Locus ID | 56603 |
UniProt ID | Q9NR63 |
Cytogenetics | 2p13.2 |
Refseq Size | 4567 |
Refseq ORF | 1536 |
Synonyms | CYP26A2; P450RAI-2; P450RAI2; RHFCA |
Summary | This gene encodes a member of the cytochrome P450 superfamily. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. The encoded protein is localized to the endoplasmic reticulum, and functions as a critical regulator of all-trans retinoic acid levels by the specific inactivation of all-trans retinoic acid to hydroxylated forms. Mutations in this gene are associated with radiohumeral fusions and other skeletal and craniofacial anomalies, and increased levels of the encoded protein are associated with atherosclerotic lesions. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2013] |
Protein Families | Druggable Genome, P450 |
Protein Pathways | Retinol metabolism |
Documents
FAQs |
SDS |
Resources
Recombinant Protein Resources |
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