AMPD1 Polyclonal Antibody | G-AB-02996

AMPD1 Polyclonal Antibody | G-AB-02996 | 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: 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

Reactivity: Human

Host: Rabbit

Isotype: IgG

Gene ID:

Accession #: NP_000027

Clonality: Polyclonal

Immunogen: Synthetic peptide of human AMPD1

Clone #:

Conjugation: Unconjugated

Swissprot: P23109

Santa Cruz: sc-160043

Calculated MW: 90 kDa

Observed MW:

Concentration: 0.5 mg/mL

Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4

Purification method: Affinity purification

Application: WB, IHC, ELISA

Dilution: WB 1:500-1:2000, IHC 1:100-1:300

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

AMPD1 Polyclonal Antibody DataSheet