AMPD1 anticorps

N° du produit ABIN7672634

Cet anticorps Lapin Polyclonal détecte spécifiquement AMPD1 dans ELISA et WB. Il présente une réactivité envers Humain, Souris et Rat.

Aperçu rapide pour AMPD1 anticorps (ABIN7672634)

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp AMPD1 est non-conjugé

Application: ELISA, Western Blotting (WB)

Détail du produit anti-AMPD1 anticorps

Fonction: AMPD1-Specific antibody

Purification: Immunogen affinity purified

Pureté: ≥95 % as determined by SDS-PAGE

Immunogène: adenosine monophosphate deaminase 1(isoform M)

Isotype: IgG

Information d'application

Indications d'application: WB: 1:500-1:5000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,

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.

Conseil sur la manipulation: Avoid repeated freeze / thaw cycles.

Stock: -20 °C

Stockage commentaire: -20°C for 12 months (Avoid repeated freeze / thaw cycles.)

Date de péremption: 12 months

Détails sur AMPD1

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

Autre désignation: AMPD1

Sujet:

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

Background: AMPD1, also named as MAD and MADA, belongs to the adenosine and AMP deaminases family. AMP deaminase plays a critical role in energy metabolism. It catalyzes the reaction: AMP + H2O = IMP + NH3. Defects in AMPD1 are the cause of adenosine monophosphate deaminase deficiency muscle type(AMPDDM) which is a metabolic disorder resulting in exercise-related myopathy. The antibody is specific to AMPD1.

Poids moléculaire: 80 kDa

ID gène: 270

UniProt: P23109