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TMEM2 Antikörper

This anti-TMEM2 antibody (ABIN7270962) is a Rabbit Polyclonal antibody detecting TMEM2 in WB. Suitable for Human.
Produktnummer ABIN7270962

Kurzübersicht für TMEM2 Antikörper (ABIN7270962)

Target

Alle TMEM2 Antikörper anzeigen
TMEM2 (Transmembrane Protein 2 (TMEM2))

Reaktivität

  • 10
  • 6
  • 4
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
Human

Wirt

  • 12
Kaninchen

Klonalität

  • 12
Polyklonal

Konjugat

  • 9
  • 1
  • 1
  • 1
Dieser TMEM2 Antikörper ist unkonjugiert

Applikation

  • 6
  • 5
  • 2
  • 2
Western Blotting (WB)
  • Verwendungszweck

    TMEM2 Rabbit pAb

    Kreuzreaktivität

    Maus, Ratte

    Produktmerkmale

    Polyclonal Antibodies

    Aufreinigung

    Affinity purification

    Immunogen

    Recombinant protein of human TMEM2.

    Isotyp

    IgG
  • Applikationshinweise

    WB,1:500 - 1:2000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Lagerung

    -20 °C

    Informationen zur Lagerung

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

    TMEM2 (Transmembrane Protein 2 (TMEM2))

    Andere Bezeichnung

    TMEM2

    Hintergrund

    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

    Gen-ID

    23670

    UniProt

    Q9UHN6
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