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Invitrogen™ PYGL Polyclonal Antibody

Rabbit Polyclonal Antibody
Brand: Invitrogen™ PA5100029
This item is not returnable.
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Description
Antibody detects endogenous levels of total 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.
Specifications
| PYGL | |
| Polyclonal | |
| Unconjugated | |
| PYGL | |
| glycogen liver; Glycogen phosphorylase, liver form; GPLL; GSD6; Lgp; liver glycogen phosphorylase; phosphorylase, glycogen, liver; PYGL | |
| Rabbit | |
| Affinity chromatography | |
| RUO | |
| 110095, 5836, 64035 | |
| -20°C | |
| Liquid |
| Immunohistochemistry (Paraffin), Western Blot | |
| 1 mg/mL | |
| PBS with 50% glycerol and 0.02% sodium azide; pH 7.4 | |
| P06737, P09811, Q9ET01 | |
| PYGL | |
| A synthesized peptide derived from human PYGL(Accession P06737), corresponding to amino acid residues G205-L255. | |
| 100 μL | |
| Primary | |
| Human, Mouse, Rat | |
| Antibody | |
| IgG |
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