|Other Accession||NP_001071159.1, NP_001071160.1, NP_001071158.1, NP_079016.2|
|Other Names||Alpha-1, 2-mannosyltransferase ALG9, Asparagine-linked glycosylation protein 9 homolog, Disrupted in bipolar disorder protein 1, Dol-P-Man:Man(6)GlcNAc(2)-PP-Dol alpha-1, 2-mannosyltransferase, Dol-P-Man:Man(8)GlcNAc(2)-PP-Dol alpha-1, 2-mannosyltransferase, ALG9, DIBD1|
|Format||Synthetic peptide was lyophilized with 100% acetonitrile and is supplied as a powder. Reconstitute with 0.1 ml DI water for a final concentration of 1 mg/ml.|
|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.|
|Function||Catalyzes the transfer of mannose from Dol-P-Man to lipid-linked oligosaccharides.|
|Cellular Location||Endoplasmic reticulum membrane; Multi-pass membrane protein|
|Tissue Location||Ubiquitously expressed; with highest levels in heart, liver and pancreas.|
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This gene encodes an alpha-1,2-mannosyltransferase enzymethat functions in lipid-linked oligosaccharide assembly. Mutationsin this gene result in congenital disorder of glycosylation typeIl. Multiple transcript variants encoding different isoforms havebeen found for this gene.
Vleugels, W., et al. Glycobiology 19(8):910-917(2009)Baysal, B.E., et al. Behav Brain Funct 2, 25 (2006) :Weinstein, M., et al. Am. J. Med. Genet. A 136(2):194-197(2005)Frank, C.G., et al. Am. J. Hum. Genet. 75(1):146-150(2004)Baysal, B.E., et al. Neurogenetics 4(1):43-53(2002)
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