PYGM Polyclonal 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.

• Description :

  This is a PYGM Polyclonal Antibody from Reddot Biotech. This product is for Research Use Only.

• Synonyms :

  Glycogen phosphorylase, Glycogen phosphorylase muscle form, muscle form, Muscpho, Myophosphorylase, Phosphorylase glycogen muscle (McArdle syndrome glycogen storage disease type V), Pygm, PYGM

• Swiss Prot :

  P11217

• Accession Number :

  BC126392

• Reactivity :

  Human, Mouse, Rat

• Immunogen :

  Recombinant protein of human PYGM

• Clonality :

  Polyclonal

• Conjugation :

  Unconjugated

• Type :

  Polyclonal Antibody

• Applications :

  WB, IHC, ELISA

• Purification Method :

  Affinity purification

• Assay Type :

  Antibody

• Concentration :

  0.4 mg/mL

• Dilution :

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

• Buffer :

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

• Storage Conditions :

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

• Calculated Molecular Weight :

  97 kDa

• Host or Source :

  Rabbit

• Isotype :

  IgG