AGL, CT (AGL, GDE, Glycogen debranching enzyme, Glycogen debrancher, 4-alpha-glucanotransferase, Oligo-1,4-1,4-glucantransferase, Amylo-alpha-1,6-glucosidase, Dextrin 6-alpha-D-glucosidase)
Référence 031698-200ul
Conditionnement : 200ul
Marque : US Biological
031698 AGL, CT (AGL, GDE, Glycogen debranching enzyme, Glycogen debrancher, 4-alpha-glucanotransferase, Oligo-1,4-1,4-glucantransferase, Amylo-alpha-1,6-glucosidase, Dextrin 6-alpha-D-glucosidase)
Clone Type
PolyclonalHost
rabbitSource
humanSwiss Prot
P35573Isotype
IgGGrade
PurifiedApplications
E IF WBCrossreactivity
HuGene #
AGLShipping Temp
Blue IceStorage Temp
-20°CAGL 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.
Applications:
Suitable for use in Western Blot, Immunofluorescence, ELISA
Recommended Dilution:
ELISA: 1:1,000
Western Blot1:100-500
Immunofluorescence: 1:10-50
Storage and Stability:
May be stored at 4°C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20°C. Aliquots are stable for 12 months. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.

