AMPD1 polyclonal, anti-human

Background:
Adenosine monophosphate deaminase 1 catalyzes the deamination of AMP to IMP in skeletal muscle and plays an important role in the purine nucleotide cycle. Two other genes have been identified, AMPD2 and AMPD3, for the liver- and erythocyte-specific isoforms, respectively. Deficiency of the muscle-specific enzyme is apparently a common cause of exercise-induced myopathy and probably the most common cause of metabolic myopathy in the human. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.

Synonyms: MAD, MADA

Cellular Location: Cytoplasm

Immunogen:
A synthetic peptide of human AMPD1

Gene Symbol: AMPD1

Gene ID: 270

Swiss prot: P23109

Calculated MW: 90kDa

Recommended dilution:
WB 1:1000-5000, IHC 1:100-300,

Purity:
Affinity purification

Storage Buffer:
Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3.

Storage:
Store at -20℃. Avoid freeze / thaw cycles.