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NLRP3 anticorps (Biotin)

Cet anticorps anti-NLRP3 est un anticorps Souris Monoclonal détectant NLRP3 dans WB, IHC, IP, ICC et ChIP. Adapté pour Humain et Souris.
N° du produit ABIN7566438

Aperçu rapide pour NLRP3 anticorps (Biotin) (ABIN7566438)

Antigène

Voir toutes NLRP3 Anticorps
NLRP3 (NLR Family, Pyrin Domain Containing 3 (NLRP3))

Reactivité

  • 90
  • 43
  • 30
  • 14
  • 5
  • 2
  • 1
  • 1
  • 1
Humain, Souris

Hôte

  • 82
  • 16
  • 2
  • 1
Souris

Clonalité

  • 77
  • 24
Monoclonal

Conjugué

  • 54
  • 8
  • 7
  • 6
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp NLRP3 est conjugé à/à la Biotin

Application

  • 56
  • 40
  • 19
  • 15
  • 15
  • 11
  • 9
  • 5
  • 5
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunoprecipitation (IP), Immunocytochemistry (ICC), Chromatin Immunoprecipitation (ChIP)

Clone

Cryo-2
  • Fonction

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

    Attributs du produit

    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).

    Purification

    Puified

    Pureté

    >95 % (SDS-PAGE)

    Immunogène

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

    Isotype

    IgG2b
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    In PBS containing 0.02 % Proclin300.

    Conseil sur la manipulation

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

    Stock

    4 °C,-20 °C

    Stockage commentaire

    +4°C

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

  • Antigène

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

    Autre désignation

    NLRP3/NALP3

    Pathways

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