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