AMPD1 Polyclonal Antibody

Sizes: 50μL, 100μL

Catalogue Numbers: RA21841-50, RA21841-100

Citations, Manuals and MSDS Available upon request.

Background: adenosine monophosphate deaminase 1 (AMPD1) Homo sapiens 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.[provided by RefSeq, Feb 2010],

Condition: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

Storage Instructions: -20°C/1 year

Recommended dilutions: Immunohistochemistry: 1/100 - 1/300. ELISA: 1/40000. Not yet tested in other applications.

Alternative Names: AMPD1; AMP deaminase 1; AMP deaminase isoform M; Myoadenylate deaminase

Applications: IHC-p; IF (paraffin section) ; ELISA

Species Cross-Reactivity: Human; Mouse; Rat

GeneID (Human): 270

SWISS: P23109

Source: Rabbit

Research Use Only