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Asparagine-Linked Glycosylation 1, beta-1,4-Mannosyltransferase Homolog (S. Cerevisiae) (ALG1) (Center) Peptide

Name

Asparagine-Linked Glycosylation 1, beta-1,4-Mannosyltransferase Homolog (S. Cerevisiae) (ALG1)
Synonyms HMT1, HMAT1, HMT-1, MGC18946, zgc:66221, wu:fi34b12
Binding Site

Center
3 references available
Certificates ISO 9001:2008
Catalog no. ABIN698922
Quantity 0.1 mg
Price 49.50 $   Plus shipping costs $45.00
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Characteristics Blocking peptide for ALG1 (Center) antibody ABIN653272
Comments

Background: The enzyme encoded by this protein catalyzes the first mannosylation step in the biosynthesis of lipid-linked oligosaccharides. This protein is mutated in congenital disorder of glycosylation type Ik.

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Storage Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles
Restrictions For Research Use only

Publications
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Product Grubenmann, Frank, Hülsmeier et al.: "Deficiency of the first mannosylation step in the N-glycosylation pathway causes congenital disorder of glycosylation type Ik." in: Human molecular genetics, Vol. 13, Issue 5, pp. 535-42, 2004 (PubMed).

Schwarz, Thiel, Lübbehusen et al.: "Deficiency of GDP-Man:GlcNAc2-PP-dolichol mannosyltransferase causes congenital disorder of glycosylation type Ik." in: American journal of human genetics, Vol. 74, Issue 3, pp. 472-81, 2004 (PubMed).

Kranz, Denecke, Lehle et al.: "Congenital disorder of glycosylation type Ik (CDG-Ik): a defect of mannosyltransferase I." in: American journal of human genetics, Vol. 74, Issue 3, pp. 545-51, 2004 (PubMed).