AMPD3 rabbit pAb - ES5545

AMPD3 rabbit pAb

Sizes: 50μL, 100μL

Catalogue Numbers: ES5545-50, ES5545-100

Citations, Manuals and MSDS Available upon request.

Background: This gene encodes a member of the AMP deaminase gene family. The encoded protein is a highly regulated enzyme that catalyzes the hydrolytic deamination of adenosine monophosphate to inosine monophosphate, a branch point in the adenylate catabolic pathway. This gene encodes the erythrocyte (E) isoforms, whereas other family members encode isoforms that predominate in muscle (M) and liver (L) cells. Mutations in this gene lead to the clinically asymptomatic, autosomal recessive condition erythrocyte AMP deaminase deficiency. Alternatively spliced transcript variants encoding different isoforms of this gene have been described. [provided by RefSeq, Jul 2008],

Alternate Name: AMPD3; AMP deaminase 3; AMP deaminase isoform E; Erythrocyte AMP 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: Synthesized peptide derived from AMPD3 . at AA range: 280-360

Storage and Stability: -20°C/1 year

Clonality: Polyclonal

Isotype: IgG

Concentration: 1 mg/ml

Human Gene ID: 272

Human SWISS Prot NO: Q01432

Subcellular Location: cytosol,

Research Use Only