PYGM antibody

Catalog No. ABIN2430685

Product Details anti-PYGM Antibody

Target: PYGM (Phosphorylase, Glycogen, Muscle (PYGM))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PYGM antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (IHC), ELISA

Purification: Affinity purification

Immunogen: Recombinant protein of human PYGM

Isotype: IgG

Application Details

Application Notes: WB 1:500-1:2000, IHC 1:30-1:150

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.4 mg/mL

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

Preservative: Sodium azide

Handling Advice: Avoid freeze / thaw cycles.

Storage: -20 °C

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

Target Details for PYGM

Target: PYGM (Phosphorylase, Glycogen, Muscle (PYGM))

Alternative Name: PYGM (PYGM Products)

Synonyms: pygb antibody, im:7150327 antibody, zgc:110706 antibody, AI115133 antibody, PG antibody, Muscpho antibody, zgc:63642 antibody, phosphorylase, glycogen, muscle L homeolog antibody, glycogen phosphorylase, muscle associated antibody, phosphorylase, glycogen, muscle A antibody, glycogen phosphorylase, muscle form antibody, muscle glycogen phosphorylase antibody, phosphorylase, glycogen, muscle b antibody, pygm.L antibody, PYGM antibody, pygma antibody, THA_70 antibody, Pygm antibody, pygmb antibody

Background: This gene encodes a muscle enzyme involved in glycogenolysis. Highly similar enzymes encoded by different genes are found in liver and brain. Mutations in this gene are associated with McArdle disease (myophosphorylase deficiency), a glycogen storage disease of muscle. Alternative splicing results in multiple transcript variants.

Molecular Weight: Calculated MW: 97 kDa

Pathways: Cellular Glucan Metabolic Process