PMGT1 Rabbit Polyclonal Antibody

Ab type

Primary 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.

Reactivity

Human, Mouse, Rat

Clonality

Polyclonal

Host

Rabbit

Isotype

IgG

Immunogen

Synthesized peptide derived from human PMGT1

Storage Stability

-20°C for 1 year

Concentration

1 mg/ml

MolecularWeight_Da

72600

synonyms

PMGT1