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YTHDF2 anticorps

Cet anticorps Lapin Polyclonal détecte spécifiquement YTHDF2 dans IHC. Il présente une réactivité envers Humain, Souris et Rat.
N° du produit ABIN7258512

Aperçu rapide pour YTHDF2 anticorps (ABIN7258512)

Antigène

Voir toutes YTHDF2 Anticorps
YTHDF2 (YTH Domain Family, Member 2 (YTHDF2))

Reactivité

  • 24
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 23
  • 2
Lapin

Clonalité

  • 24
  • 1
Polyclonal

Conjugué

  • 15
  • 3
  • 2
  • 2
  • 2
  • 1
Cet anticorp YTHDF2 est non-conjugé

Application

  • 21
  • 14
  • 5
  • 4
  • 2
  • 1
  • 1
  • 1
Immunohistochemistry (IHC)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogène

    Recombinant fusion protein of human YTHDF2 (NP_057342.2).

    Isotype

    IgG
  • Indications d'application

    IHC 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

    YTHDF2 (YTH Domain Family, Member 2 (YTHDF2))

    Autre désignation

    YTHDF2

    Sujet

    This gene encodes a member of the YTH (YT521-B homology) superfamily containing YTH domain. The YTH domain is typical for the eukaryotes and is particularly abundant in plants. The YTH domain is usually located in the middle of the protein sequence and may function in binding to RNA. In addition to a YTH domain, this protein has a proline rich region which may be involved in signal transduction. An Alu-rich domain has been identified in one of the introns of this gene, which is thought to be associated with human longevity. In addition, reciprocal translocations between this gene and the Runx1 (AML1) gene on chromosome 21 has been observed in patients with acute myeloid leukemia. This gene was initially mapped to chromosome 14, which was later turned out to be a pseudogene. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.

    ID gène

    51441

    UniProt

    Q9Y5A9
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