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WDR4 Antikörper

Dieses Anti-WDR4-Antikörper ist ein Kaninchen Monoklonal-Antikörper zur Detektion von WDR4 in WB und IHC. Geeignet für Human.
Produktnummer ABIN7271355

Kurzübersicht für WDR4 Antikörper (ABIN7271355)

Target

Alle WDR4 Antikörper anzeigen
WDR4 (WD Repeat Domain 4 (WDR4))

Reaktivität

  • 31
  • 12
  • 5
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Wirt

  • 29
  • 2
Kaninchen

Klonalität

  • 28
  • 3
Monoklonal

Konjugat

  • 19
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser WDR4 Antikörper ist unkonjugiert

Applikation

  • 23
  • 9
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Verwendungszweck

    WDR4 Rabbit mAb

    Kreuzreaktivität

    Human, Maus, Ratte

    Produktmerkmale

    Monoclonal Antibodies

    Aufreinigung

    Affinity purification

    Immunogen

    A synthesized peptide derived from human WDR4

    Isotyp

    IgG
  • Applikationshinweise

    WB,1:500 - 1:2000,IHC,1:50 - 1:200

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,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

    WDR4 (WD Repeat Domain 4 (WDR4))

    Andere Bezeichnung

    WDR4

    Hintergrund

    This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This gene is excluded as a candidate for a form of nonsyndromic deafness (DFNB10), but is still a candidate for other disorders mapped to 21q22.3 as well as for the development of Down syndrome phenotypes. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, May 2012],TRM82, TRMT82,Epigenetics & Nuclear Signaling,WDR4

    Molekulargewicht

    45kDa

    Gen-ID

    10785

    UniProt

    P57081
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