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

AdipoGen Life Sciences

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

10

ImmunoPrecipitation, Western Blot, ChIP Chromatin ImmunoPrecipitation, ImmunoCytoChemistry, ImmunoHistoChemistry

Research Use Only

Monoclonal

Cryo-2

1 mg/ml

>95%

Nlrp3

NLR family, pyrin domain containing 3

AGTAVPRL, AII/AVP, Cias1, FCAS, FCU, MWS, Mmig1, NALP3, Pypaf1, NACHT, LRR and PYD domains-containing protein 3, NACHT/LRR/pyrin domain-containing protein 3, PYRIN-containing APAF1-like protein 1, cold autoinflammatory syndrome 1 protein homolog, cryopyrin, mast cell maturation-associated-inducible protein 1

Mouse

IgG2b

NACHT, LRR and PYD domains-containing protein 3

Monoclonal Antibody. Recognizes mouse and human NLRP3/NALP3. Isotype: Mouse IgG2b. Clone: Cryo-2. Applications: IHC, IP, WB. Liquid. In PBS containing 10% glycerol and 0.02% sodium azide. 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).

-20°C,2°C to 8°C

12352203