AGL polyclonal, anti-human, mouse

Background:
This gene encodes the glycogen debrancher enzyme which is involved in glycogen degradation. This enzyme has two independent catalytic activities which occur at different sites on the protein: a 4-alpha-glucotransferase activity and a amylo-1,6-glucosidase activity. Mutations in this gene are associated with glycogen storage disease although a wide range of enzymatic and clinical variability occurs which may be due to tissue-specific alternative splicing. Alternatively spliced transcripts encoding different isoforms have been described. 

Synonyms: GDE

Cellular Location: Cytoplasm

Immunogen:
A synthetic peptide of human AGL

Gene Symbol: AGL

Gene ID: 178

Swiss prot: P35573

Calculated MW: 175 kDa

Recommended dilution:
WB 1:200-1000, IHC 1:30-150,

Purity:
Affinity purification

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

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