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B3GAT2 Antibody (Center) Blocking Peptide
Synthetic peptide
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
| Primary Accession | Q9NPZ5 |
|---|---|
| Other Accession | NP_542780.1 |
| Clone Names | 90826058 |
| Gene ID | 135152 |
|---|---|
| Other Names | Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 2, Beta-1, 3-glucuronyltransferase 2, GlcAT-D, UDP-glucuronosyltransferase S, GlcAT-S, Glucuronosyltransferase S, B3GAT2, GLCATS, KIAA1963 |
| Format | Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed. |
| Storage | Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C. |
| Precautions | This product is for research use only. Not for use in diagnostic or therapeutic procedures. |
| Name | B3GAT2 |
|---|---|
| Synonyms | GLCATS, KIAA1963 |
| Function | Involved in the biosynthesis of L2/HNK-1 carbohydrate epitope on both glycolipids and glycoproteins. |
| Cellular Location | Golgi apparatus membrane; Single-pass type II membrane protein |
| Tissue Location | Expressed in the trachea, retina, spinal cord, hippocampus and other brain regions, and, at lower levels, in testis and ovary |
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Provided below are standard protocols that you may find useful for product applications.
Background
The product of this gene is a transmembrane proteinbelonging to the glucuronyltransferase family, and catalyzes thetransfer of a beta-1,3 linked glucuronic acid to a terminalgalactose in different glycoproteins or glycolipids containing aGal-beta-1-4GlcNAc or Gal-beta-1-3GlcNAc residue. The encodedprotein is involved in the synthesis of the human natural killer-1(HNK-1) carbohydrate epitope, a sulfated trisaccharide implicatedin cellular migration and adhesion in the nervous system. [providedby RefSeq].
References
Bailey, S.D., et al. Diabetes Care (2010) In press :Talmud, P.J., et al. Am. J. Hum. Genet. 85(5):628-642(2009)Shiba, T., et al. Proteins 65(2):499-508(2006)Kakuda, S., et al. Glycobiology 15(2):203-210(2005)Kakuda, S., et al. Protein Expr. Purif. 35(1):111-119(2004)
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