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