AMPD1 anticorps (AA 261-310)

N° du produit ABIN1534626

Cet anticorps Lapin Polyclonal détecte spécifiquement AMPD1 dans ELISA, IHC et IF. Il présente une réactivité avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour AMPD1 anticorps (AA 261-310) (ABIN1534626)

Antigène: AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp AMPD1 est non-conjugé

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

Détail du produit anti-AMPD1 anticorps

Épitope: AA 261-310

Fonction: AMPD1 Antibody

Specificité: AMPD1 Polyclonal Antibody detects endogenous levels of AMPD1 protein.

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

Pureté: > 95 %

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

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

Concentration: 1 mg/mL

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 AMPD1

Antigène: AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))

Autre désignation: AMPD1

Sujet:

Synonyms: AMPD1, AMP deaminase 1, AMP deaminase isoform M, Myoadenylate deaminase

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],

Gene Name: AMPD1

Protein Name: AMP deaminase 1

Poids moléculaire: 86 kDa

ID gène: 270

OMIM: 102770

UniProt: P23109