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WDR4 Antikörper

Dieser 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

  • 40
  • 12
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Wirt

  • 38
  • 2
Kaninchen

Klonalität

  • 28
  • 12
Monoklonal

Konjugat

  • 19
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser WDR4 Antikörper ist unkonjugiert

Applikation

  • 32
  • 15
  • 13
  • 11
  • 11
  • 10
  • 3
  • 3
  • 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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