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WRB Antikörper

WRB Reaktivität: Maus, Ratte IHC Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7262941
  • Target Alle WRB Antikörper anzeigen
    WRB (Tryptophan Rich Basic Protein (WRB))
    Reaktivität
    • 13
    • 2
    • 1
    Maus, Ratte
    Wirt
    • 8
    • 5
    • 1
    Kaninchen
    Klonalität
    • 12
    • 2
    Polyklonal
    Konjugat
    • 10
    • 2
    • 1
    • 1
    Dieser WRB Antikörper ist unkonjugiert
    Applikation
    • 10
    • 8
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Immunohistochemistry (IHC)
    Produktmerkmale
    Polyclonal Antibody
    Aufreinigung
    Affinity purification
    Immunogen
    Recombinant fusion protein of human WRB (NP_004618.2).
    Isotyp
    IgG
    Top Product
    Discover our top product WRB Primärantikörper
  • Applikationshinweise
    IHC 1:50-1:200
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 mg/mL
    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
    WRB (Tryptophan Rich Basic Protein (WRB))
    Andere Bezeichnung
    WRB (WRB Produkte)
    Synonyme
    pwi antikoerper, wu:ft06h05 antikoerper, zgc:101856 antikoerper, chd5 antikoerper, MGC89989 antikoerper, WRB antikoerper, UCP-1 antikoerper, DKFZp469L094 antikoerper, wrb antikoerper, mCHD5 antikoerper, MGC115192 antikoerper, CHD5 antikoerper, 5530402J05Rik antikoerper, C030018G21Rik antikoerper, Chd5 antikoerper, tryptophan rich basic protein antikoerper, tryptophan rich basic protein L homeolog antikoerper, WRB antikoerper, wrb antikoerper, wrb.L antikoerper, Wrb antikoerper
    Hintergrund
    This gene encodes a basic nuclear protein of unknown function. The gene is widely expressed in adult and fetal tissues. Since the region proposed to contain the gene(s) for congenital heart disease (CHD) in Down syndrome (DS) patients has been restricted to 21q22.2-22.3, this gene, which maps to 21q22.3, has a potential role in the pathogenesis of Down syndrome congenital heart disease. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
    Gen-ID
    7485
    UniProt
    O00258
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