Synthesized peptide derived from human PMGT1 AA range: 171-221
Storage:
-20C/1 year
Clonality:
Polyclonal
Isotype:
IgG
Concentration:
1 mg/ml
Molecular Weight:
73kD
GeneID:
55624
Human Swiss-Prot No:
Q8WZA1
Cellular localization:
Golgi apparatus membrane ; Single-pass type II membrane protein .
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. [provided by RefSeq, Feb 2014],