This gene encodes a type II transmembrane protein that resides in the Golgi apparatus. It participates in O-mannosyl glycosylation and is specific for alpha linked terminal mannose. Mutations in this gene may be associated with muscle-eye-brain disease and several congenital muscular dystrophies. Alternatively spliced transcript variants that encode different protein isoforms have been described.
Immunogen Information
Immunogen
Fusion protein of human POMGNT1
Swissprot
Q8WZA1
Synonyms
2-N-acetylglucosaminyltransferase 12-N-acetylglucosaminyltransferase I.2GnT I.2GnTI.2MEBMGAT 1.2MGAT1.2O linked mannose beta1 2 N acetylglucosaminyltransferasePMGT1POMGNT 1POMGnT1Protein O linked mannose beta 1 2 N acetylglucosaminyltransferase
Calculated MW
75 kDa
Observed MW
Refer to figures
Gene Accession
BC001471
Applications
Reactivity
Human, Mouse, Rat
Tested Applications
WB,ELISA
Conjugation
Unconjugated
Dilution
WB 1:500-1:2000, ELISA 1:5000-1:10000
Concentration
0.72 mg/mL
Storage Buffer
PBS with 0.05% NaN3 and 40% Glycerol, pH7.4
Storage Instructions
Store at -20°C. Avoid freeze / thaw cycles.
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