POMT1 polyclonal, anti-human, mouse

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.

Synonyms: LGMD2K, MDDGA1, MDDGB1, MDDGC1, RT

Cellular Location: Endoplasmic reticulum membrane Multi-pass membrane protein

Immunogen:
Recombinant protein of human POMT1

Gene Symbol: POMT1

Gene ID: 10585

Swiss prot: Q9Y6A1

Calculated MW: 85kDa

Recommended dilution:
WB 1:1000-2000

Purity:
Affinity purification

Storage Buffer:
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

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