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Rabbit Anti-AMPD1 PAb

Product Description

  • Type:
  • Polyclonal Antibody
  • Source:
  • Rabbit
  • Species:
  • Human
  • Application:
  • ELISA; WB; IHC
  • Description:
  • Swissprot P23109; Gene Accession NP_000027
  • Format:
  • Liquid
  • Concentration:
  • Please refer to the vial lable for the specific concentration.
  • Purification:
  • Protein A/G
  • Buffer:
  • Supplied in PBS.
  • Storage:
  • Short Term: 2-8 degree. Long Term: -20 degree. Avoid multiple freeze-thaw cycles.

General Information

  • 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:
  • adenosine monophosphate deaminase 1,MAD; MADA

Documents

Order Details

Cat No:ABSPA-0620

Conjugate:ABSPA-0620

Size:1 mg

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  • +1 929 202 3014
  • info@abvigenus.com