POMT1 Polyclonal Antibody

Background:
The protein encoded by this gene is an O-mannosyltransferase that requires interaction with the product of the POMT2 gene for enzymatic function. The encoded protein is found in the membrane of the endoplasmic reticulum. Defects in this gene are a cause of Walker-Warburg syndrome (WWS) and limb-girdle muscular dystrophy type 2K (LGMD2K). Several transcript variants encoding different isoforms have been found for this gene.

Research Area: Cancer, Neuroscience, Signal Transduction

Synonyms:
Dolichyl phosphate mannose protein mannosyltransferase 1, Dolichyl phosphate mannose protein mannosyltransferase1, Dolichyl-phosphate-mannose--protein mannosyltransferase 1, LGMD2K, MDDGA1, MDDGB1, MDDGC1, POMT 1, POMT1, POMT1, Protein O mannosyl transferase 1, Protein O mannosyl transferase1, Protein O-mannosyl-transferase 1, Rotate abdomen, Drosophila, homolog of, RT

Immunogen: Synthetic peptide of human POMT1

Swissprot: Q9Y6A1
Gene Accession: NP_001070833

Purification Method: Affinity purification

Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4

Concentration: 0.4 mg/mL
Dilution: IHC 1:50-1:200

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

Alternative for product with catalog number:
sc-48914/sc-48915/sc-98908