Mannosyl Alpha-1,6-Glycoprotein Beta-1,2-N-Acetylglucosaminyltransferase (MGAT2)

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CDGS2; GNT2; Beta-1,2-N-acetylglucosaminyltransferase II; Mannoside acetylglucosaminyltransferase 2; N-glycosyl-oligosaccharide-glycoprotein N-acetylglucosaminyltransferase II

Mannosyl Alpha-1,6-Glycoprotein Beta-1,2-N-Acetylglucosaminyltransferase (MGAT2)
MGAT2 is a Golgi enzyme catalyzing an essential step in the conversion of oligomannose to complex N-glycans. The enzyme has the typical glycosyltransferase domains: a short N-terminal cytoplasmic domain, a hydrophobic non-cleavable signal-anchor domain, and a C-terminal catalytic domain. Mutations in this gene may lead to carbohydrate-deficient glycoprotein syndrome, type II. The coding region of this gene is intronless. The predicted 447-amino acid GlcNAc-T II protein has the typical glycosyltransferase domains: a short (9-amino acid) N-terminal cytoplasmic domain, a 20-amino acid hydrophobic noncleavable signal-anchor domain, and a C-terminal catalytic domain. On Northern blots, GlcNAc-T II was transcribed as a major 3.0-kb mRNA, with minor bands at 2 and 4.5 kb, in all tissues tested.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Mannosyl Alpha-1,6-Glycoprotein Beta-1,2-N-Acetylglucosaminyltransferase (MGAT2) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Mannosyl Alpha-1,6-Glycoprotein Beta-1,2-N-Acetylglucosaminyltransferase (MGAT2) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Mannosyl Alpha-1,6-Glycoprotein Beta-1,2-N-Acetylglucosaminyltransferase (MGAT2) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Mannosyl Alpha-1,6-Glycoprotein Beta-1,2-N-Acetylglucosaminyltransferase (MGAT2) CLIA Kit Customized Service Offer
n/a ELISA Kit for Mannosyl Alpha-1,6-Glycoprotein Beta-1,2-N-Acetylglucosaminyltransferase (MGAT2) ELISA Kit Customized Service Offer

Organism species: Mus musculus (Mouse)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Mannosyl Alpha-1,6-Glycoprotein Beta-1,2-N-Acetylglucosaminyltransferase (MGAT2) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Mannosyl Alpha-1,6-Glycoprotein Beta-1,2-N-Acetylglucosaminyltransferase (MGAT2) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Mannosyl Alpha-1,6-Glycoprotein Beta-1,2-N-Acetylglucosaminyltransferase (MGAT2) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Mannosyl Alpha-1,6-Glycoprotein Beta-1,2-N-Acetylglucosaminyltransferase (MGAT2) CLIA Kit Customized Service Offer
n/a ELISA Kit for Mannosyl Alpha-1,6-Glycoprotein Beta-1,2-N-Acetylglucosaminyltransferase (MGAT2) ELISA Kit Customized Service Offer

Organism species: Rattus norvegicus (Rat)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Mannosyl Alpha-1,6-Glycoprotein Beta-1,2-N-Acetylglucosaminyltransferase (MGAT2) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Mannosyl Alpha-1,6-Glycoprotein Beta-1,2-N-Acetylglucosaminyltransferase (MGAT2) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Mannosyl Alpha-1,6-Glycoprotein Beta-1,2-N-Acetylglucosaminyltransferase (MGAT2) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Mannosyl Alpha-1,6-Glycoprotein Beta-1,2-N-Acetylglucosaminyltransferase (MGAT2) CLIA Kit Customized Service Offer
n/a ELISA Kit for Mannosyl Alpha-1,6-Glycoprotein Beta-1,2-N-Acetylglucosaminyltransferase (MGAT2) ELISA Kit Customized Service Offer
  1. "The human UDP-N-acetylglucosamine: alpha-6-D-mannoside-beta-1,2-N-acetylglucosaminyltransferase II gene (MGAT2). Cloning of genomic DNA, localization to chromosome 14q21, expression in insect cells and purification of the recombinant protein."Eur. J. Biochem. 231:317-328(1995) [PubMed] [Europe PMC] [Abstract]
  2. "Complete sequencing and characterization of 21,243 full-length human cDNAs." Nat. Genet. 36:40-45(2004) [PubMed] [Europe PMC] [Abstract]
  3. "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
  4. "Mutations in the MGAT2 gene controlling complex N-glycan synthesis cause carbohydrate-deficient glycoprotein syndrome type II, an autosomal recessive disease with defective brain development."Am. J. Hum. Genet. 59:810-817(1996) [PubMed] [Europe PMC] [Abstract]
  5. "Congenital disorders of glycosylation IIa cause growth retardation, mental retardation, and facial dysmorphism."J. Med. Genet. 37:875-877(2000) [PubMed] [Europe PMC] [Abstract]