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