AMPD3 antibody (AA 280-360)

Catalog No. ABIN8119596

The Rabbit Polyclonal anti-AMPD3 antibody is suitable to detect AMPD3 in samples from Human, Mouse and Rat. It has been validated for IF, IHC and ELISA.

Quick Overview for AMPD3 antibody (AA 280-360) (ABIN8119596)

Target: AMPD3 (Adenosine Monophosphate Deaminase 3 (AMPD3))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This AMPD3 antibody is un-conjugated

Application: Immunofluorescence (IF), Immunohistochemistry (IHC), ELISA

Product Details anti-AMPD3 Antibody

Binding Specificity: AA 280-360

Purpose: AMPD3 Antibody

Specificity: AMPD3 Polyclonal Antibody detects endogenous levels of AMPD3 protein.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogen: Synthesized peptide derived from AMPD3 . at AA range: 280-360

Isotype: IgG

Application Details

Application Notes: IHC 1:100 - 1:300. ELISA: 1:40000.. IF 1:50-200

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C/1 year

Expiry Date: 12 months

Target Details for AMPD3

Target: AMPD3 (Adenosine Monophosphate Deaminase 3 (AMPD3))

Alternative Name: AMPD3

Background:

Synonyms: AMPD3, AMP deaminase 3, AMP deaminase isoform E, Erythrocyte AMP deaminase

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],

Gene Name: AMPD3

Protein Name: AMP deaminase 3

Gene ID: 272

UniProt: Q01432