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AMPD3 anticorps

Cet anticorps anti-AMPD3 est un anticorps Lapin Polyclonal détectant AMPD3 dans IF. Adapté pour Humain.
N° du produit ABIN7257022

Aperçu rapide pour AMPD3 anticorps (ABIN7257022)

Antigène

Voir toutes AMPD3 Anticorps
AMPD3 (Adenosine Monophosphate Deaminase 3 (AMPD3))

Reactivité

  • 47
  • 23
  • 20
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 33
  • 14
Lapin

Clonalité

  • 32
  • 14
Polyclonal

Conjugué

  • 19
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp AMPD3 est non-conjugé

Application

  • 25
  • 13
  • 12
  • 11
  • 10
  • 8
  • 7
  • 7
  • 5
  • 2
  • 1
  • 1
  • 1
Immunofluorescence (IF)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogène

    Recombinant fusion protein of human AMPD3 (NP_000471.1).

    Isotype

    IgG
  • Indications d'application

    IF 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    PBS with 0.02 % sodium azide, 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.

    Stock

    -20 °C

    Stockage commentaire

    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène

    AMPD3 (Adenosine Monophosphate Deaminase 3 (AMPD3))

    Autre désignation

    AMPD3

    Sujet

    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.

    ID gène

    272

    UniProt

    Q01432
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