PYGM 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.

• NCBI Gene ID :

  5837

• Swiss Prot :

  P11217

• Host :

  Rabbit

• Reactivity :

  Human, Mouse, Rat

• Immunogen :

  A synthetic peptide corresponding to a sequence within amino acids 700 to the C-terminus of human PYGM (NP_005600.1) .

• Clonality :

  Polyclonal

• Conjugation :

  Unconjugated

• Type :

  Primary Antibodies

• Field of Research :

  Cancer, Signal Transduction

• Purification :

  Affinity purification

• Positive Control :

  Mouse skeletal muscle

• Concentration :

  Batch dependent

• Buffer :

  PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

• Modification :

  None

• Shipping Conditions :

  Blue Ice

• Storage Conditions :

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

• Calculated Molecular Weight :

  Observed: 100kDa

• Fragment :

  IgG

• Applications Notes :

  WB: 1:500 - 1:2000

• Symbol :

  PYGM

• Positive Control 2 :

  Mouse brain

• Positive Control 3 :

  Mouse lung

• Positive Control 4 :

  Rat skeletal muscle

• NCBI Official Name :

  Phosphorylase, glycogen, muscle

• NCBI Organism :

  Homo sapiens

• Other Product Names :

  PYGM, GPMM, Myophosphorylase, Phosphorylase, glycogen muscle

• Tested Applications :

  WB

• Physical Properties :

  Liquid