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NSJ Bioreagents

SKU:RQ8505

4-Alpha-glucanotransferase Antibody / AGL / Glycogen debranching enzyme

4-Alpha-glucanotransferase Antibody / AGL / Glycogen debranching enzyme

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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.

Specifications

Family Primary antibody
Formulation 0.5mg/ml if reconstituted with 0.2ml sterile DI water
Format Antigen affinity purified
Host Animal Rabbit
Clonality Polyclonal (rabbit origin)
Isotype Rabbit IgG
Species Reactivity Human, Mouse, Rat
Application WB, IHC-P, IF, FACS, ELISA
Application Details Western blot: 0.5-1ug/ml,Immunohistochemistry (FFPE): 2-5ug/ml,Immunofluorescence: 5ug/ml,Flow cytometry: 1-3ug/million cells,ELISA: 0.1-0.5ug/ml
Application Note Optimal dilution of the 4-Alpha-glucanotransferase antibody should be determined by the researcher.
Immunogen An E.coli-derived human recombinant protein (amino acids H3-K265) was used as the immunogen for the 4-Alpha-glucanotransferase antibody.
Buffer Lyophilized from 1X PBS with 2% Trehalose
Purity Antigen affinity purified
Storage After reconstitution, the 4-Alpha-glucanotransferase antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
Limitation This 4-Alpha-glucanotransferase antibody is available for research use only.
Uniprot # P35573
Status Available
PDF Link https://www.nsjbio.com/tds-pdf/4-alpha-glucanotransferase-antibody-agl-glycogen-debranching-enzyme-rq8505
Title 4-Alpha-glucanotransferase Antibody / AGL / Glycogen debranching enzyme
Description 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.
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