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ALG2 Antibody (Center) Blocking Peptide
Synthetic peptide
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
| Primary Accession | Q9H553 |
|---|---|
| Clone Names | 100623214 |
| Gene ID | 85365 |
|---|---|
| Other Names | Alpha-1, 3/1, 6-mannosyltransferase ALG2, Asparagine-linked glycosylation protein 2 homolog, GDP-Man:Man(1)GlcNAc(2)-PP-Dol alpha-1, 3-mannosyltransferase, GDP-Man:Man(1)GlcNAc(2)-PP-dolichol mannosyltransferase, GDP-Man:Man(2)GlcNAc(2)-PP-Dol alpha-1, 6-mannosyltransferase, ALG2 |
| 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 | ALG2 |
|---|---|
| Function | Mannosylates Man(2)GlcNAc(2)-dolichol diphosphate and Man(1)GlcNAc(2)-dolichol diphosphate to form Man(3)GlcNAc(2)-dolichol diphosphate. |
| Cellular Location | Membrane; Single-pass membrane protein |
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Provided below are standard protocols that you may find useful for product applications.
Background
This gene encodes a member of the glycosyltransferase 1family. The encoded protein acts as an alpha 1,3mannosyltransferase, mannosylating Man(2)GlcNAc(2)-dolicholdiphosphate and Man(1)GlcNAc(2)-dolichol diphosphate to formMan(3)GlcNAc(2)-dolichol diphosphate. Defects in this gene havebeen associated with congenital disorder of glycosylation type Ih(CDG-Ii). Alternative splicing results in multiple transcriptvariants.
References
Inuzuka, T., et al. BMC Struct. Biol. 10, 25 (2010) :Okumura, M., et al. Biochem. Biophys. Res. Commun. 386(1):237-241(2009)Hoj, B.R., et al. Biochem. Biophys. Res. Commun. 378(1):145-148(2009)Mahul-Mellier, A.L., et al. J. Biol. Chem. 283(50):34954-34965(2008)la Cour, J.M., et al. Mol Oncol 1(4):431-439(2008)
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