Description
AMPD1 Polyclonal Antibody | E-AB-12967 | Gentaur UK, US & Europe Distribution
Type: Polyclonal Antibody
Synonyms: Adenosine monophosphate deaminase 1 (isoform M), Adenosine monophosphate deaminase 1, AMP deaminase 1, AMP deaminase isoform M, AMPD 1, AMPD, Ampd01, MAD, MADA, Myoadenylate deaminase, RATAMPD01, Skeletal muscle AMPD
Application: WB, IHC, ELISA
Reactivity: Human
Host: Rabbit
Isotype: IgG
Reserch Areas: Cancer, Metabolism, Signal Transduction
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.
Concentration: 1 mg/mL
Storage: Store at -20°C. Avoid freeze / thaw cycles.
Immunogen: Synthetic peptide of human AMPD1
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Purification Method: Affinity purification
Dilution: WB 1:1000-1:5000, IHC 1:100-1:300
Clone: N/A
Conjugation: Unconjugated
Molecular Weight(Calculated): 90 kDa
Molecular Weight(Observed): N/A