NLRP3 Recombinant Rabbit mAb
Cat No.: ARM2558
Size:
Product Name: | NLRP3 Recombinant Rabbit mAb |
Cat No.: | ARM2558 |
source: | Rabbit |
reactivity: | Human, Mouse, Rat |
applications: | WB |
clonality: | Monoclonal |
recommended dilution: | WB |
format: | Liquid |
isotype: | IgG |
immunogen: | Recombinant protein of human NLRP3 |
calculated molecular weight: | 118 kDa |
observed molecular weight: | 118 kDa |
genbank accession number: | Q96P20 |
gene id (ncbi): | 114548 |
purification method: | Affinity Purification |
conjugate: | Un-conjugated |
storage: | Store at -20°C. Supplied in 50nM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide and 0.05% BSA. Stable for 12 months from date of receipt. |
synonyms: | AII; AVP; FCU; MWS; FCAS; CIAS1; FCAS1; NALP3; C1orf7; CLR1.1; PYPAF1; AGTAVPRL |
category: | Primary Ab |
concentration: | 1mg/ml |
background: | This gene encodes a pyrin-like protein containing a pyrin domain, a nucleotide-binding site (NBS) domain, and a leucine-rich repeat (LRR) motif. This protein interacts with the apoptosis-associated speck-like protein PYCARD/ASC, which contains a caspase recruitment domain, and is a member of the NALP3 inflammasome complex. This complex functions as an upstream activator of NF-kappaB signaling, and it plays a role in the regulation of inflammation, the immune response, and apoptosis. Mutations in this gene are associated with familial cold autoinflammatory syndrome (FCAS), Muckle-Wells syndrome (MWS), chronic infantile neurological cutaneous and articular (CINCA) syndrome, and neonatal-onset multisystem inflammatory disease (NOMID). Multiple alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. Alternative 5-- UTR structures are suggested by available data; however, insufficient evidence is available to determine if all of the represented 5-- UTR splice patterns are biologically valid. [provided by RefSeq, Oct 2008] |