PYGL Polyclonal Antibody | G-AB-01159

PYGL Polyclonal Antibody | G-AB-01159 | Gentaur Antibodies

Overview: 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.

Category Type: Polyclonal Antibody

Research Areas: Cancer, Metabolism, Signal Transduction

Synonyms: Glycogen phosphorylase, Glycogen phosphorylase L, Glycogen phosphorylase liver, Glycogen phosphorylase liver form, GSD6, Hers disease, glycogen storage disease type VI, liver form, OTTHUMP00000233649, OTTHUMP00000233651, Phosphorylase glycogen liver, Pygl, PYGL

Reactivity: Human, Mouse, Rat

Host: Rabbit

Isotype: IgG

Gene ID:

Accession #: BC082229

Clonality: Polyclonal

Immunogen: Recombinant protein of human PYGL

Clone #:

Conjugation: Unconjugated

Swissprot: P06737

Santa Cruz: sc-46347/sc-66913

Calculated MW: 97 kDa

Observed MW:

Concentration: 0.4 mg/mL

Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4

Purification method: Affinity purification

Application: WB, IHC, ELISA

Dilution: WB 1:500-1:2000, IHC 1:30-1:150

Storage: Store at -20°C. Avoid freeze / thaw cycles.

PYGL Polyclonal Antibody DataSheet