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NLRP2 Antikörper (AA 425-475)

NLRP2 Reaktivität: Human WB, IP, IHC (fp) Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7453735
  • Target Alle NLRP2 Antikörper anzeigen
    NLRP2 (NLR Family, Pyrin Domain Containing 2 (NLRP2))
    Bindungsspezifität
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 425-475
    Reaktivität
    • 33
    • 10
    • 6
    • 1
    • 1
    • 1
    • 1
    Human
    Wirt
    • 24
    • 7
    • 2
    • 1
    Kaninchen
    Klonalität
    • 28
    • 6
    Polyklonal
    Konjugat
    • 34
    Dieser NLRP2 Antikörper ist unkonjugiert
    Applikation
    • 30
    • 10
    • 6
    • 6
    • 5
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunoprecipitation (IP), Immunohistochemistry (Formalin-fixed Paraffin-embedded Sections) (IHC (fp))
    Verwendungszweck
    Rabbit anti-NBS1 Antibody, Affinity Purified
    Homologie
    Orangutan
    Aufreinigung
    Affinity Purified
    Immunogen
    between AA 425 and 475
    Isotyp
    IgG
    Top Product
    Discover our top product NLRP2 Primärantikörper
  • Applikationshinweise

    IHC: 1:100 - 1:500. Epitope retrieval with citrate buffer pH 6.0 is recommended for FFPE tissue sections.

    IP: 2 - 5 μg/mg lysate

    WB: 1:2,000 - 1:10,000

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Konzentration
    200 μg/mL
    Buffer
    Tris-buffered Saline containing 0.1 % BSA and 0.09 % Sodium Azide
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    4 °C
    Haltbarkeit
    12 months
  • Target
    NLRP2 (NLR Family, Pyrin Domain Containing 2 (NLRP2))
    Andere Bezeichnung
    NBS1 (NLRP2 Produkte)
    Hintergrund
    Background: Mutations in NBS1 (Nijmegen Breakage Syndrome 1), also known as nibrin, are associated with the autosomal recessive syndrome, Nijmegen breakage syndrome, characterized by microcephaly, growth retardation, immunodeficiency, and cancer predisposition. At the cellular level, NBS1 is part of the MRE11/RAD50 double-strand break repair complex that is critical to the DNA damage response, DNA recombination, telomere integrity, and cell cycle checkpoint control.
    Gen-ID
    4683
    NCBI Accession
    NP_002476
    UniProt
    O60934
    Pathways
    Production of Molecular Mediator of Immune Response, Positive Regulation of Endopeptidase Activity, Inflammasome
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