ASAH1 polyclonal, anti-human, mouse, rat

Background:
This gene encodes a heterodimeric protein consisting of a nonglycosylated alpha subunit and a glycosylated beta subunit that is cleaved to the mature enzyme posttranslationally. The encoded protein catalyzes the synthesis and degradation of ceramide into sphingosine and fatty acid. Mutations in this gene have been associated with a lysosomal storage disorder known as Farber disease. Multiple transcript variants encoding several distinct isoforms have been identified for this gene.

Synonyms: AC, PHP, ASAH, PHP32, ACDase, SMAPME

Cellular Location: Cytoplasm

Immunogen:
Recombinant protein of human ASAH1

Gene Symbol: ASAH1

Gene ID: 427

Swiss prot: Q13510

Calculated MW: 45kDa

Recommended dilution:
WB 1:500-2000, IHC 1:20-100,

Purity:
Affinity purification

Storage Buffer:
Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3.

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