|Western Blot (WB)||1:1000|
|Tested Species reactivity||Human|
|Host / Isotype||Rabbit / IgG|
|Immunogen||KLH conjugated synthetic peptide between 1479-1510 amino acids from the C-terminal region of human AGL|
|Purification||Ammonium sulfate precipitation, Size-exclusion - Dialysis|
|Contains||0.09% sodium azide|
|Storage conditions||-20° C, Avoid Freeze/Thaw Cycles|
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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: 4-alpha-glucanotransferase; amylo-1, 6-glucosidase, 4-alpha-glucanotransferase; Amylo-1,6-glucosidase; amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferaseprovided; Amylo-alpha-1,6-glucosidase; Dextrin 6-alpha-D-glucosidase; GDE; Glycogen debrancher; Glycogen debranching enzyme; glycogen debranching protein; Oligo-1,4-1,4-glucantransferase
Gene Aliases: AGL; GDE
UniProt ID: (Human) P35573
Entrez Gene ID: (Human) 178
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