Search results for PYGL antibody

PYGL antibody, Genetex, GTX33448

Anti-PYGL antibody, Abcam, AB103419

Anti-PYGL antibody, Abcam, AB198268

Anti-PYGL antibody, Abcam, AB223788

Glycogen Phosphorylase, Liver (PYGL) Antibody, Abbexa, abx103000

Polyclonal Antibody to Glycogen Phosphorylase, Liver (PYGL).

Glycogen Phosphorylase, Liver (PYGL) Antibody, Abbexa, abx405488

This product is currently in development. The lead time for this product may be several months. Please contact us at [email protected] for an updated lead time before purchasing this product. Rat Glycogen Phosphorylase, Liver (PYGL) Antibody is a Mouse monoclonal against Glycogen Phosphorylase, Liver (PYGL).

Glycogen Phosphorylase, Liver (PYGL) Antibody, Abbexa, abx236975

PYGL Antibody is a Rabbit Polyclonal against PYGL.

Glycogen Phosphorylase, Liver (PYGL) Antibody, Abbexa, abx103002

Polyclonal Antibody to Glycogen Phosphorylase, Liver (PYGL).

Glycogen Phosphorylase, Liver (PYGL) Antibody, Abbexa, abx405489

This product is currently in development. The lead time for this product may be several months. Please contact us at [email protected] for an updated lead time before purchasing this product. Rat Glycogen Phosphorylase, Liver (PYGL) Antibody is a Mouse monoclonal against Glycogen Phosphorylase, Liver (PYGL).

Glycogen Phosphorylase, Liver (PYGL) Antibody, Abbexa, abx005147

PYGL Antibody is a Rabbit Polyclonal antibody against PYGL. This gene encodes a homodimeric protein that catalyses the cleavage of alpha-1,4-glucosidic bonds to release glucose-1-phosphate from liver glycogen stores. This protein switches from inactive phosphorylase B to active phosphorylase A by phosphorylation of serine residue 15. Activity of this enzyme is further regulated by multiple allosteric effectors and hormonal controls. Humans have three glycogen phosphorylase genes that encode distinct isozymes that are primarily expressed in liver, brain and muscle, respectively. The liver isozyme serves the glycemic demands of the body in general while the brain and muscle isozymes supply just those tissues. In glycogen storage disease type VI, also known as Hers disease, mutations in liver glycogen phosphorylase inhibit the conversion of glycogen to glucose and results in moderate hypoglycemia, mild ketosis, growth retardation and hepatomegaly. Alternative splicing results in multiple transcript variants encoding different isoforms.