Background：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.
仕様
Synonyms：2-N-acetylglucosaminyltransferase 1,2-N-acetylglucosaminyltransferase I.2,GnT I.2,GnTI.2,MEB,MGAT 1.2,MGAT1.2,O linked mannose beta1 2 N acetylglucosaminyltransferase,PMGT1,POMGNT 1,POMGnT1,Protein O linked mannose beta 1 2 N acetylglucosaminyltransferase 1,Protein O linked mannose beta1 2 N acetylglucosaminyltransferase,Protein O-linked-mannose beta-1,UDP GlcNAc,UDP GlcNAc：alpha D mannoside beta 1 2 N acetylglucosaminyltransferase I.2,UDP-GlcNAc：alpha-D-mannoside beta-1
Host：Rabbit
Reactivity：Human,Mouse,Rat
Applications：WB,IHC
Concentration：1mg/ml
Immunogen：Recombinant protein of human POMGNT1
Purification Method：Affinity purification
Clonality：Polyclonal
Conjugation：Unconjugated
Buffer：Buffer： PBS with 0.02％ sodium azide, 50％ glycerol, pH7.3.
