POMGNT1 Polyclonal Antibody

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.

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

Immunogen: Fusion protein of human POMGNT1

Swissprot: Q8WZA1
Gene Accession: BC001471

Calculated MW: 75 kDa
Observed MW: Refer to figures

Purification Method: Antigen affinity purification

Buffer: PBS with 0.05% NaN3 and 40% Glycerol, pH7.4

Concentration: 0.96 mg/mL
Dilution: WB 1:500-1:2000, IHC 1:30-1:150, ELISA 1:5000-1:10000

Storage:
Store at -20°C. Avoid freeze / thaw cycles.