- Tel: 858.663.9055
Email: info@nsjbio.com
- Tel: 858.663.9055
- Email: info@nsjbio.com
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.
The stated application concentrations are suggested starting points. Titration of the Glycogen debranching enzyme antibody may be required due to differences in protocols and secondary/substrate sensitivity.
A portion of amino acids 1479-1510 from the human protein was used as the immunogen for the Glycogen debranching enzyme antibody.
Aliquot the Glycogen debranching enzyme antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
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