PMGT1 rabbit pAb

Sizes: 50μL, 100μL

Catalogue Numbers: ES14054-50, ES14054-100

Citations, Manuals and MSDS Available upon request.

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],

Source: Rabbit

Applications: WB; IHC

Dilution: WB 1:500-2000; IHC-p 1:50-300

Reactivity: Human; Mouse; Rat

Immunogen: Synthesized peptide derived from human PMGT1 AA range: 171-221

Storage and Stability: -20°C/1 year

Clonality: Polyclonal

Isotype: IgG

Concentration: 1 mg/ml

Human Gene ID: 55624

Human SWISS Prot NO: Q8WZA1

Subcellular Location: Golgi apparatus membrane; Single-pass type II membrane protein.

Research Use Only