AMPD1 Polyclonal Antibody | G-AB-10350

AMPD1 Polyclonal Antibody | G-AB-10350 | Gentaur Antibodies

Overview: 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.

Category Type: Polyclonal Antibody

Research Areas: Cancer, Metabolism, Signal Transduction

Synonyms: AMPD1, MAD, MADA, MMDD

Reactivity: Human, Mouse, Rat

Host: Rabbit

Isotype: IgG

Gene ID: 270

Accession #:

Clonality:

Immunogen: Recombinant fusion protein of human AMPD1 (NP_001166097.1) .

Clone #:

Conjugation: Unconjugated

Swissprot: P23109

Santa Cruz:

Calculated MW: 89 kDa/90 kDa

Observed MW: 80 kDa

Concentration: 1 mg/mL

Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3

Purification method: Affinity purification

Application: WB

Dilution: WB 1:500-1:2000

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

AMPD1 Polyclonal Antibody DataSheet