兔抗AGL多克隆抗体

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.

Applications:

ELISA, WB

Name of antibody:

AGL

Immunogen:

Synthetic peptide of human AGL

Full name:

amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase

Synonyms：

GDE

SwissProt:

P35573

ELISA Recommended dilution:

1000-2000

WB Predicted band size:

175 kDa

WB Positive control:

Human fetal liver tissue

WB Recommended dilution:

200-1000