AGL Polyclonal Antibody

Store at -20C. Avoid freeze / thaw cycles.

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.

PBS with 0.05% sodium azide and 50% glycerol, pH 7.4

IHC 1:25-1:100

Synthetic peptide of human AGL