366946
CYP26C1 (Cytochrome P450 26C1, Cytochrome P450, Family 26, Subfamily C, Polypeptide 1)

Size
£800.00
- SKU:
- 366946
- Purity:
- Purified by Protein G affinity chromatography.
- Storage Conditions:
- -20°C
- Supplier:
- United States Biological
- Host:
- Mouse
- Immunogen:
- Linear peptide corresponding to human CYP26C at C-terminal, Ovalbumin conjugated. Species sequence homology: rat
- Clone:
- T6P1C7*E7
- Format:
- Supplied as a liquid in 0.1M Tris-Glycine, pH 7.4, 150mM sodium chloride, 0.05% sodium azide.
- Extra Details:
- Cytochrome P450 26C1 (UniProt Q6V0L0; also known as CYP26C1, Cytochrome P450, family 26, subfamily C, polypeptide 1) is encoded by the CYP26C1 (also known as FFDD4) gene (Gene ID 340665) in human. Cytochromes P450 (CYP) proteins are primarily membrane-associated oxidases located either in the inner membrane of mitochondria or in the endoplasmic reticulum where they function as the terminal enzymes in electron transfer chains. In addition to processing endogenous substrates, CYPs also function to metabolize exogenous drugs and potentially toxic chemicals. The human CYP superfamily consisits of 57 genes and more than 59 pseudogenes divided into 18 families and 43 subfamilies. The CYP26 subfamily of enzymes (CYP26A1, CYP26B1/CYP26A2, CYP26C1) are retinoic acid hydroxylases responsible for the inactivation of all-trans-retinoic acid (atRA) to hydroxylated forms, such as 4-oxo-, 4-OH-, and 18-OH-atRA, with 4-oxo-RA being the most common metabolite. All-trans-RA represents the most active form of RA and plays a crucial role in the development of multiple organs via its gene regulatory function. 4-oxo-9-cis-retinoic acid (9-cis-RA) and 4-oxo-13-cis-retinoic acid (13-cis-RA) are two atRA stereo-isomers that also play an important role in RA signalling. Immunohistochemistry staining reveals moderate to strong expression of CYP26A1 and CYP26B1 in colon cancer tissues when compared with normal colonic epithelium, while CYP26C1 was not expressed in either type of colon tissue samples. CYP26C1 gene mutations are linked to focal facial dermal dysplasia 4 (FFDD4), a group of developmental defects characterized by bitemporal or preauricular skin lesions resembling aplasia cutis congenita. Applications: Suitable for use in Western Blot and Immunohistochemistry. Other applications not tested. Recommended Dilutions: Western Blot: 10ug/ml detects CYP26C1 in 50ug of human liver microsome lysate. Immunohistochemistry: paraffin sections Optimal dilutions to be determined by the researcher. Storage and Stability: May be stored at 4°C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20°C. Aliquots are stable for 12 months after receipt. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
- Shipping Conditions:
- Blue Ice
