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Rabbit anti nlrp3 antibodies

Manufactured by Cell Signaling Technology
Sourced in United States

Rabbit anti-NLRP3 antibodies are primary antibodies that specifically recognize the NLRP3 protein, a key component of the NLRP3 inflammasome. These antibodies can be used to detect and study the expression and localization of NLRP3 in various biological samples.

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2 protocols using rabbit anti nlrp3 antibodies

1

Immunoblotting Analysis of Lung Proteins

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Lung tissues were homogenized to obtain protein samples with RIPA lysis buffer containing PMSF after washing with cold PBS. Then, the protein (25 μg) was separated by SDS-PAGE and transferred to PVDF membranes. The membranes were incubated overnight with appropriated primary antibody at 4°C after being blocked with 5% bovine serum albumin (BSA). Rabbit anti-ICAM-1 antibodies (1: 1000), rabbit anti-CXCR4 antibodies (1: 1000), rabbit anti-SDF-1 antibodies (1: 1000), rabbit anti-Bcl2 antibodies (1: 1000), rabbit anti-bax antibodies (1: 1000), rabbit anti-cleaved caspase3 antibodies (1: 500), rabbit anti-NLRP3 antibodies (1: 1000), rabbit anti-ASC antibodies (1: 1000), rabbit anti-pro-IL-1β antibodies (1: 1000), rabbit anti-IL-1β antibodies (1: 1000), rabbit anti-pro-caspase1 antibodies (1: 1000), and rabbit anti-caspase1 antibodies (1: 1000) were purchased from Cell Signaling Technology (Danvers, USA). Subsequently, PVDF membranes were incubated with the corresponding secondary antibodies and visualized using a Tanon-5200 Chemiluminescence Imager (Tanon, Shanghai, China) with enhanced chemiluminescence (ECL) method.
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2

Immunoprecipitation and Western Blot for ADAM8

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Equal amounts of proteins (1 mg) were precleared with protein A + G-Sepharose beads for 1 hour at 4°C and were then incubated with 2 mg rabbit anti-ADAM8 antibodies (Abbexa, Cambridge, UK) and anti-ADAM8 antibodies (Cell Signaling Technology, Massachusetts, USA) overnight at 4°C. Immune complexes were precipitated using protein A + G-Sepharose beads and were washed four times with 100 mM sodium phosphate buffer (pH 7.4). Following boiling in SDS/PAGE loading buffer, proteins were analyzed by western blot with rabbit anti-ADAM8 (Proteintech, Illinois, USA) and rabbit anti-NLRP3 antibodies (Cell Signaling Technology, Massachusetts, USA).
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