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TMEM2 anticorps

Cet anticorps anti-TMEM2 est un anticorps Lapin Polyclonal détectant TMEM2 dans WB. Adapté pour Humain.
N° du produit ABIN7270962

Aperçu rapide pour TMEM2 anticorps (ABIN7270962)

Antigène

Voir toutes TMEM2 Anticorps
TMEM2 (Transmembrane Protein 2 (TMEM2))

Reactivité

  • 9
  • 6
  • 4
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
Humain

Hôte

  • 11
Lapin

Clonalité

  • 11
Polyclonal

Conjugué

  • 8
  • 1
  • 1
  • 1
Cet anticorp TMEM2 est non-conjugé

Application

  • 6
  • 4
  • 1
  • 1
Western Blotting (WB)
  • Fonction

    TMEM2 Rabbit pAb

     Réactivité croisée

    Souris, Rat

    Attributs du produit

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogène

    Recombinant protein of human TMEM2.

    Isotype

    IgG
  • Indications d'application

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    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

    TMEM2 (Transmembrane Protein 2 (TMEM2))

    Autre désignation

    TMEM2

    Sujet

    This gene encodes a type II transmembrane protein that belongs to the interferon-induced transmembrane (IFITM) protein superfamily. The encoded protein functions as a cell surface hyaluronidase that cleaves extracellular high molecular weight hyaluronan into intermediate size fragments before internalization and degradation in the lysosome. It also has an interferon-mediated antiviral function in humans through activation of the JAK STAT signaling pathway. The activation of this gene by transcription factor SOX4 in breast cancer cells has been shown to mediate the pathological effects of SOX4 on cancer progression. Naturally occurring mutations in this gene are associated with autosomal recessive non-syndromic hearing loss. [provided by RefSeq, Mar 2017],TMEM2,Cell Biology & Developmental Biology,TMEM2

    ID gène

    23670

    UniProt

    Q9UHN6
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