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NLRP3 antibody (Biotin)

This anti-NLRP3 antibody is a Mouse Monoclonal antibody detecting NLRP3 in WB, IHC, IP, ICC and ChIP. Suitable for Human and Mouse.
Catalog No. ABIN7566438

Quick Overview for NLRP3 antibody (Biotin) (ABIN7566438)

Target

See all NLRP3 Antibodies
NLRP3 (NLR Family, Pyrin Domain Containing 3 (NLRP3))

Reactivity

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

Host

  • 75
  • 11
  • 2
  • 1
Mouse

Clonality

  • 69
  • 20
Monoclonal

Conjugate

  • 57
  • 7
  • 5
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
This NLRP3 antibody is conjugated to Biotin

Application

  • 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)

Clone

Cryo-2
  • Purpose

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

    Characteristics

    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

    Purity

    >95 % (SDS-PAGE)

    Immunogen

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

    Isotype

    IgG2b
  • Application Notes

    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.

    Handling Advice

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

    Storage

    4 °C,-20 °C

    Storage Comment

    +4°C

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

  • Target

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

    Alternative Name

    NLRP3/NALP3

    Pathways

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