AGL Polyclonal Antibody

Rs. 16,500.00
SKU E-AB-13013


Synonyms 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
Swissprot P35573
Source Rabbit
Reactivity Human
Immunogen Synthetic peptide of human AGL
Application IHC,ELISA
Recommended dilution IHC 1:25-1:100
Concentration 0.2mg/mL
Clonality Polyclonal


Cellular localization  
Tissue specificity  
Isotype IgG
Purification Affinity purification
Conjugation Unconjugated
Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
Storage buffer PBS with 0.05% sodium azide, 50% glycerol, PH7.3
Background 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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