AMPD3 anticorps (AA 280-360)

N° du produit ABIN8119596

L’anticorps anti-AMPD3 Polyclonal Lapin est utilisé pour la détection de AMPD3 dans des échantillons de Humain, Souris et Rat. Il a été validé pour IF, IHC et ELISA.

Aperçu rapide pour AMPD3 anticorps (AA 280-360) (ABIN8119596)

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp AMPD3 est non-conjugé

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

Détail du produit anti-AMPD3 anticorps

Épitope: AA 280-360

Fonction: AMPD3 Antibody

Specificité: 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.

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

Isotype: IgG

Information d'application

Indications d'application: IHC 1:100 - 1:300. ELISA: 1:40000.. IF 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

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

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C/1 year

Date de péremption: 12 months

Détails sur AMPD3

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

Autre désignation: AMPD3

Sujet:

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

ID gène: 272

UniProt: Q01432