Synonyms: Anti-4-alpha-glucanotransferase; Anti-Amylo-alpha-1,6-glucosidase; Anti-Glycogen debrancher; Anti-Glycogen debranching enzyme; Oligo-1,4-1,4-glucantransferase
Storage: -20C
UNSPSC Code: 12352203
General description: AGL is a 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 the AGL 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.
Immunogen: AGL (NP_000019, 1483-1520)This antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide selected from the C-terminal region of human AGL.
Physical form: Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide.
RIDADR: NONH for all modes of transport
WGK Germany: nwg