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Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase

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Adds the first glucose residue to the lipid-linked oligosaccharide precursor for N-linked glycosylation. Transfers glucose from dolichyl phosphate glucose (Dol-P-Glc) onto the lipid-linked oligosaccharide Man(9)GlcNAc(2)-PP-Dol (By similarity).

Below are the list of possible Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase products. If you cannot find the target and/or product is not available in our catalog, please click here to contact us and request the product or submit your request for custom elisa kit production, custom recombinant protein production or custom antibody production. Custom ELISA Kits, Recombinant Proteins and Antibodies can be designed, manufactured and produced according to the researcher's specifications.
 

Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase

 Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase ELISA Kit
 Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase Recombinant
 Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase Antibody
Also known as Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase (Asparagine-linked glycosylation protein 6 homolog) (Dol-P-Glc:Man(9)GlcNAc(2)-PP-Dol alpha-1,3-glucosyltransferase) (Dolichyl-P-Glc:Man9GlcNAc2-PP-dolichyl glucosyltransferas.
ALG6: Adds the first glucose residue to the lipid-linked oligosaccharide precursor for N-linked glycosylation. Transfers glucose from dolichy
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l phosphate glucose (Dol-P-Glc) onto the lipid-linked oligosaccharide Man(9)GlcNAc(2)-PP-Dol. Defects in ALG6 are the cause of congenital disorder of glycosylation type 1C (CDG1C); also known as carbohydrate-deficient glycoprotein syndrome type V. CDGs are metabolic deficiencies in glycoprotein biosynthesis that usually cause severe mental and psychomotor retardation. They are characterized by under-glycosylated serum glycoproteins. CDG1C patients have muscular hypotonia, show a delayed statomotor development and are mentally retarded. CDG1C is biochemically characterized by an accumulation of dolichyl pyrophosphate-linked Man(9)GlcNAc(2) in the endoplasmic reticulum. Belongs to the ALG6/ALG8 glucosyltransferase family.

Protein type: EC 2.4.1.267; Glycan Metabolism - N-glycan biosynthesis; Membrane protein, integral; Membrane protein, multi-pass; Transferase

Cellular Component: endoplasmic reticulum membrane; membrane

Molecular Function: dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase activity; glucosyltransferase activity

Biological Process: oligosaccharide-lipid intermediate assembly; protein amino acid N-linked glycosylation
 Alg6 ELISA Kit
 Alg6 Recombinant
 Alg6 Antibody
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