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SNX29 Antikörper

RUNDC2A Reaktivität: Human IHC, ELISA Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7192586
  • Target Alle SNX29 (RUNDC2A) Produkte
    SNX29 (RUNDC2A) (RUN Domain Containing 2A (RUNDC2A))
    Reaktivität
    • 29
    • 4
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human
    Wirt
    • 27
    • 2
    Kaninchen
    Klonalität
    • 27
    • 2
    Polyklonal
    Konjugat
    • 12
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser SNX29 Antikörper ist unkonjugiert
    Applikation
    • 21
    • 17
    • 16
    • 3
    • 2
    Immunohistochemistry (IHC), ELISA
    Kreuzreaktivität
    Human, Maus
    Aufreinigung
    Antigen affinity purification
    Immunogen
    Synthetic peptide of Human SNX29
    Isotyp
    IgG
  • Applikationshinweise
    ELISA:1:1000-1:2000, IHC:1:20-1:100,
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Buffer
    -20 °C, pH 7.4 PBS, 0.05 % Sodium azide, 40 % Glycerol
    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,-80 °C
    Informationen zur Lagerung
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • Target
    SNX29 (RUNDC2A) (RUN Domain Containing 2A (RUNDC2A))
    Andere Bezeichnung
    SNX29 (RUNDC2A Produkte)
    Synonyme
    RUNDC2A antikoerper, 4933437K13Rik antikoerper, ENSMUSG00000079738 antikoerper, Gm11170 antikoerper, Gm1737 antikoerper, Gm930 antikoerper, Rundc2a antikoerper, RGD1565890 antikoerper, A-388D4.1 antikoerper, RUN domain containing 2A antikoerper, sorting nexin 29 antikoerper, sorting nexin-29 antikoerper, RUNDC2A antikoerper, Snx29 antikoerper, SNX29 antikoerper, LOC104975843 antikoerper
    Hintergrund

    Background: SNX29 also known as RUNDC2A, is a 375 amino protein that contains one RUN domain. RUNDC2A is encoded by a gene that maps to human chromosome 16p13.13, which encodes over 900 genes and comprises nearly 3 % of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.

    Aliases: SNX29 antibody, RUNDC2A antibody, Sorting nexin-29 antibody, RUN domain-containing protein 2A antibody

    UniProt
    Q8TEQ0
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