Anti-Human AGL Polyclonal Antibody

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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Properties

Data Sheet Click for Datasheet
Catalog Number PA09282
Size 100μl
Host Type Rabbit
Immunogen Synthetic peptide of human AGL
Specificity Liver, kidney and lymphoblastoid cells express predominantly isoform 1; whereas muscle and heart express not only isoform 1, but also muscle-specific isoform mRNAs (isoforms 2, 3 and 4). Isoforms 5 and 6 are present in both liver and muscle.
Isotype IgG
Reacitivity Human
Clone
Uniprot P35573
Concentration 0.2 mg/mL
Dilution IHC 1:25-1:100
Formulation
Application IHC,ELISA
Other Names 1110061O17Rik,4-1,4-glucantransferase,6-glucosidase,9430004C13Rik,9630046L06Rik,AGL,AI850929,Amylo 1 6 glucosidase 4 alpha glucanotransferase,Amylo-1,Amylo-alpha-1,C77197,Dextrin 6-alpha-D-glucosidase,GDE,GDE,Glycogen debrancher,Glycogen debranching enzyme,Glycogen storage disease type III,Oligo-1
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.

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