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AMPD1 Polyclonal Antibody

Product Specifications

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.

Abbreviation

AMPD1

UniProt

P23109

Host

Rabbit

Reactivity

Human

Immunogen

Synthetic peptide of human AMPD1

Target

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

Clonality

Polyclonal

Conjugation

Unconjugated

Applications

WB; IHC

Field of Research

Cancer; Metabolism; Signal Transduction

Purification

Affinity purification

Concentration

1 mg/mL

Dilution

WB 1:1000-1:5000; IHC 1:100-1:300

Buffer

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

Shipping Conditions

The product is shipped with ice pack, upon receipt, store it immediately at the temperature recommended.

Storage Conditions

Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.

Calculated Molecular Weight

90kDa

Isotype

IgG

Available Sizes

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