NLRP3 Polyclonal antibody proteintech 19771-1-AP

$449.00
In stock
SKU
19771-1-AP

 

Angiotensin/vasopressin receptor AII/AVP-like, C1orf7, CIAS1, Cold-induced autoinflammatory syndrome 1 protein, EC:3.6.4.-

Host / Isotype: Rabbit / IgG Class: Polyclonal
Reactivity: Human And More (3) Immunogen: Peptide Predict reactive species
 Applications: WB, IHC, IF/ICC, FC (Intra), IP, CoIP, ELISA, Cell treatment Observed Molecular Weight: 118 kDa
Formulation: PBS, Azide, Glycerol GenBank Accession Number: NM_001127461
Conjugate: Unconjugated Gene Symbol: NLRP3
Tested Applications: Positive WB detected in Gene ID (NCBI): 114548
Application: Western Blot (WB) RRID: AB_10646484
Dilution: WB : 1:500-1:2000 Conjugate: Unconjugated
Tested Reactivity: Human Form: Liquid
Host / Isotype: Rabbit / IgG Background Information: NALP3, also named C1orf7, CIAS1, and PYPAF1, belongs to the NLRP family. NLRP3, a key and eponymous component of the NLRP3 inflammasome, plays a crucial role in innate immunity and inflammation. NALP3 may function as an inducer of apoptosis. It interacts selectively with ASC and this complex may function as an upstream activator of NF-kappa-B signaling.NALP3 inhibits TNF-alpha-induced activation and nuclear translocation of RELA/NF-KB p65. Also inhibits transcriptional activity of RELA. NALP3 activates caspase-1 in response to a number of triggers including bacterial or viral infection which leads to processing and release of IL1B and IL18. Defects in NLRP3 are the cause of familial cold autoinflammatory syndrome type 1 (FCAS1) which is also known as familial cold urticaria. Defects in NLRP3 are a cause of Muckle-Wells syndrome (MWS) which is urticaria-deafness-amyloidosis syndrome. Defects in NLRP3 are the cause of chronic infantile neurologic cutaneous and articular syndrome (CINCA) which is also known as neonatal onset multisystem inflammatory disease (NOMID). The antibody recognizes the C-term of NALP3.

 

 

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