Mouse Peroxisome Proliferator Activated Receptor Gamma (PPAR-γ) ELISA Kit

PPAR-G ELISA Kit, PPARG1 ELISA Kit, PPARG2 ELISA Kit, NR1C3 ELISA Kit, Glitazone Receptor ELISA Kit, Nuclear Receptor Subfamily 1 Group C Member 3 ELISA Kit

Runhong Zhou 1, Ruifeng Huang 2, Shaofen Zhou 2, Shengsheng Lu 2, Haixing Lin 2, Jingnan Qiu 2, Shuaiqi Ma 2, Jian He Sorbicillinoid HSL-2 inhibits the infection of influenza A virus via interaction with the PPAR-γ/NF-κB pathway J Infect Chemother, (2024), Haiwei Ni # 1, Zachary J Reitman # 2, Wei Zou 1, Md Naushad Akhtar 1, Ritama Paul 1, Menggui Huang 1, Duo Zhang 1, Hao Zheng 1, Ruitao Zhang 1, Ruiying Ma 1, Gina Ngo 1, Lin Zhang 3, Eric S Diffenderfer 1, S Azar Oliaei Motlagh 1, Michele M Kim 1, Andy J Minn 1 4, Jay F Dorsey 1, Jessica B Foster 5, James Metz 1, Constantinos Koumenis 1 4, David G Kirsch 6 7 8 9, Yanqing Gong 10, Yi Fan FLASH radiation reprograms lipid metabolism and macrophage immunity and sensitizes medulloblastoma to CAR-T cell therapy Nat Cancer ., (2025)

Standard: 10 ng/mL. Test principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Mouse PPAR-γ. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Mouse PPAR-γ. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Mouse PPAR-γ, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Mouse PPAR-γ in the samples is then determined by comparing the OD of the samples to the standard curve