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NLRP3 Antikörper (Biotin)

Dieses Anti-NLRP3-Antikörper ist ein Maus Monoklonal-Antikörper zur Detektion von NLRP3 in WB, IHC, IP, ICC und ChIP. Geeignet für Human und Maus.
Produktnummer ABIN7566438

Kurzübersicht für NLRP3 Antikörper (Biotin) (ABIN7566438)

Target

Alle NLRP3 Antikörper anzeigen
NLRP3 (NLR Family, Pyrin Domain Containing 3 (NLRP3))

Reaktivität

  • 75
  • 32
  • 18
  • 6
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Maus

Wirt

  • 75
  • 11
  • 2
  • 1
Maus

Klonalität

  • 69
  • 20
Monoklonal

Konjugat

  • 57
  • 7
  • 5
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
Dieser NLRP3 Antikörper ist konjugiert mit Biotin

Applikation

  • 55
  • 42
  • 16
  • 14
  • 10
  • 9
  • 6
  • 5
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunoprecipitation (IP), Immunocytochemistry (ICC), Chromatin Immunoprecipitation (ChIP)

Klon

Cryo-2
  • Verwendungszweck

    anti-NLRP3/NALP3, mAb (Cryo-2) (Biotin)

    Produktmerkmale

    Monoclonal Antibody. Recognizes mouse and human NLRP3/NALP3. Applications: IHC, IP, WB. Clone: Cryo-2. Isotype: Mouse IgG2b. Liquid. In PBS containing 0.02 % Proclin300. The inflammasome is a multiprotein complex that mediates the activation of caspase-1, which promotes, amongst others, the secretion of the proinflammatory cytokines interleukin (IL)-1beta and IL-18. Members of the Nod-like receptor family, including NLRP3/NALP3, are critical components of the inflammasome that link danger-signals to caspase-1 activation. Defects in NLRP3 are the cause of familial cold autoinflammatory syndrome type 1 (FCAS1), Muckle-Wells syndrome (MWS) and of chronic infantile neurologic cutaneous and articular syndrome (CINCA).

    The inflammasome is a multiprotein complex that mediates the activation of caspase-1, which promotes, amongst others, the secretion of the proinflammatory cytokines interleukin (IL)-1beta and IL-18. Members of the Nod-like receptor family, including NLRP3/NALP3, are critical components of the inflammasome that link danger-signals to caspase-1 activation. Defects in NLRP3 are the cause of familial cold autoinflammatory syndrome type 1 (FCAS1), Muckle-Wells syndrome (MWS) and of chronic infantile neurologic cutaneous and articular syndrome (CINCA).

    Aufreinigung

    Puified

    Reinheit

    >95 % (SDS-PAGE)

    Immunogen

    Recombinant mouse NLRP3/NALP3 (pyrin domain/aa 1-93).

    Isotyp

    IgG2b
  • Applikationshinweise

    Optimal working dilution should be determined by the investigator.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    1 mg/mL

    Buffer

    In PBS containing 0.02 % Proclin300.

    Handhabung

    After opening, prepare aliquots and store at -20 °C.Avoid freeze/thaw cycles.

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    +4°C

    Stable for at least 1 year after receipt when stored at -20°C.

  • Target

    NLRP3 (NLR Family, Pyrin Domain Containing 3 (NLRP3))

    Andere Bezeichnung

    NLRP3/NALP3

    Pathways

    Cellular Response to Molecule of Bacterial Origin, Positive Regulation of Endopeptidase Activity, Inflammasome
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