AMPD1 rabbit pAb - ES5526

AMPD1 rabbit pAb

Sizes: 50μL, 100μL

Catalogue Numbers: ES5526-50, ES5526-100

Citations, Manuals and MSDS Available upon request.

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.[provided by RefSeq, Feb 2010],

Alternate Name: AMPD1; AMP deaminase 1; AMP deaminase isoform M; Myoadenylate deaminase

Source: Rabbit

Applications: IHC; IF; ELISA

Dilution: Immunohistochemistry: 1/100 - 1/300. ELISA: 1/40000. Not yet tested in other applications.

Reactivity: Human; Mouse; Rat

Immunogen: The antiserum was produced against synthesized peptide derived from human AMPD1. AA range:261-310

Storage and Stability: -20°C/1 year

Clonality: Polyclonal

Isotype: IgG

Concentration: 1 mg/ml

Human Gene ID: 270

Human SWISS Prot NO: P23109

Subcellular Location: cytosol,

Research Use Only