cl097 Search Results


cl097  (InvivoGen)
95
InvivoGen cl097
Cl097, supplied by InvivoGen, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/cl097/product/InvivoGen
Average 95 stars, based on 1 article reviews
cl097 - by Bioz Stars, 2026-03
95/100 stars
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cl097  (MedChemExpress)
93
MedChemExpress cl097
(A) iBMDMs were primed with LPS and stimulated with 5 mM ATP over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation and GSDMD cleavage. (B) iBMDMs were primed with LPS and stimulated with 70 μM <t>CL097</t> over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation and GSDMD cleavage. (C) WT and caspase-1 knockout (CASP1 −/− ) iBMDMs were primed with LPS and stimulated with 10 μM nigericin over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation and GSDMD cleavage. (D) WT and GSDMD knockout (GSDMD −/− ) iBMDMs were primed with LPS and stimulated with 10 μM nigericin over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation. (E) Primary BMDMs were generated from WT and GSDMD knockout (GSDMD −/− ) C57BL/6 mice. BMDMs were then primed with LPS and stimulated with 10μM nigericin over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation. (F) Primary BMDMs were generated from WT and NLRP3 knockout (NLRP3 −/− ) C57BL/6 mice. BMDMs were then primed with LPS and stimulated with 10 μM nigericin over a time course of 45 min. Cellular lysates were examined by western blot for changes in signaling pathway phosphorylation. (G) iBMDMs were primed with LPS and stimulated with 10 μM nigericin or 10 μM rotenone over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation and GSDMD cleavage. (H) iBMDMs were primed with LPS and stimulated with 10 μM nigericin or 10 μM carbonyl cyanide- p -trifluoromethoxyphenylhydrazone (FCCP) over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation and GSDMD cleavage. All western blots are representative of at least three independent experiments.
Cl097, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/cl097/product/MedChemExpress
Average 93 stars, based on 1 article reviews
cl097 - by Bioz Stars, 2026-03
93/100 stars
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cl097  (Autogen-Bioclear ltd)
90
Autogen-Bioclear ltd cl097
(A) iBMDMs were primed with LPS and stimulated with 5 mM ATP over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation and GSDMD cleavage. (B) iBMDMs were primed with LPS and stimulated with 70 μM <t>CL097</t> over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation and GSDMD cleavage. (C) WT and caspase-1 knockout (CASP1 −/− ) iBMDMs were primed with LPS and stimulated with 10 μM nigericin over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation and GSDMD cleavage. (D) WT and GSDMD knockout (GSDMD −/− ) iBMDMs were primed with LPS and stimulated with 10 μM nigericin over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation. (E) Primary BMDMs were generated from WT and GSDMD knockout (GSDMD −/− ) C57BL/6 mice. BMDMs were then primed with LPS and stimulated with 10μM nigericin over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation. (F) Primary BMDMs were generated from WT and NLRP3 knockout (NLRP3 −/− ) C57BL/6 mice. BMDMs were then primed with LPS and stimulated with 10 μM nigericin over a time course of 45 min. Cellular lysates were examined by western blot for changes in signaling pathway phosphorylation. (G) iBMDMs were primed with LPS and stimulated with 10 μM nigericin or 10 μM rotenone over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation and GSDMD cleavage. (H) iBMDMs were primed with LPS and stimulated with 10 μM nigericin or 10 μM carbonyl cyanide- p -trifluoromethoxyphenylhydrazone (FCCP) over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation and GSDMD cleavage. All western blots are representative of at least three independent experiments.
Cl097, supplied by Autogen-Bioclear ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/cl097/product/Autogen-Bioclear ltd
Average 90 stars, based on 1 article reviews
cl097 - by Bioz Stars, 2026-03
90/100 stars
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tlrl c97  (InvivoGen)
94
InvivoGen tlrl c97
(A) iBMDMs were primed with LPS and stimulated with 5 mM ATP over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation and GSDMD cleavage. (B) iBMDMs were primed with LPS and stimulated with 70 μM <t>CL097</t> over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation and GSDMD cleavage. (C) WT and caspase-1 knockout (CASP1 −/− ) iBMDMs were primed with LPS and stimulated with 10 μM nigericin over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation and GSDMD cleavage. (D) WT and GSDMD knockout (GSDMD −/− ) iBMDMs were primed with LPS and stimulated with 10 μM nigericin over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation. (E) Primary BMDMs were generated from WT and GSDMD knockout (GSDMD −/− ) C57BL/6 mice. BMDMs were then primed with LPS and stimulated with 10μM nigericin over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation. (F) Primary BMDMs were generated from WT and NLRP3 knockout (NLRP3 −/− ) C57BL/6 mice. BMDMs were then primed with LPS and stimulated with 10 μM nigericin over a time course of 45 min. Cellular lysates were examined by western blot for changes in signaling pathway phosphorylation. (G) iBMDMs were primed with LPS and stimulated with 10 μM nigericin or 10 μM rotenone over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation and GSDMD cleavage. (H) iBMDMs were primed with LPS and stimulated with 10 μM nigericin or 10 μM carbonyl cyanide- p -trifluoromethoxyphenylhydrazone (FCCP) over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation and GSDMD cleavage. All western blots are representative of at least three independent experiments.
Tlrl C97, supplied by InvivoGen, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/tlrl c97/product/InvivoGen
Average 94 stars, based on 1 article reviews
tlrl c97 - by Bioz Stars, 2026-03
94/100 stars
  Buy from Supplier

Image Search Results


(A) iBMDMs were primed with LPS and stimulated with 5 mM ATP over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation and GSDMD cleavage. (B) iBMDMs were primed with LPS and stimulated with 70 μM CL097 over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation and GSDMD cleavage. (C) WT and caspase-1 knockout (CASP1 −/− ) iBMDMs were primed with LPS and stimulated with 10 μM nigericin over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation and GSDMD cleavage. (D) WT and GSDMD knockout (GSDMD −/− ) iBMDMs were primed with LPS and stimulated with 10 μM nigericin over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation. (E) Primary BMDMs were generated from WT and GSDMD knockout (GSDMD −/− ) C57BL/6 mice. BMDMs were then primed with LPS and stimulated with 10μM nigericin over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation. (F) Primary BMDMs were generated from WT and NLRP3 knockout (NLRP3 −/− ) C57BL/6 mice. BMDMs were then primed with LPS and stimulated with 10 μM nigericin over a time course of 45 min. Cellular lysates were examined by western blot for changes in signaling pathway phosphorylation. (G) iBMDMs were primed with LPS and stimulated with 10 μM nigericin or 10 μM rotenone over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation and GSDMD cleavage. (H) iBMDMs were primed with LPS and stimulated with 10 μM nigericin or 10 μM carbonyl cyanide- p -trifluoromethoxyphenylhydrazone (FCCP) over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation and GSDMD cleavage. All western blots are representative of at least three independent experiments.

Journal: Cell reports

Article Title: Restraint of inflammasome-driven cytokine responses through the mRNA stability protein TTP

doi: 10.1016/j.celrep.2025.115340

Figure Lengend Snippet: (A) iBMDMs were primed with LPS and stimulated with 5 mM ATP over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation and GSDMD cleavage. (B) iBMDMs were primed with LPS and stimulated with 70 μM CL097 over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation and GSDMD cleavage. (C) WT and caspase-1 knockout (CASP1 −/− ) iBMDMs were primed with LPS and stimulated with 10 μM nigericin over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation and GSDMD cleavage. (D) WT and GSDMD knockout (GSDMD −/− ) iBMDMs were primed with LPS and stimulated with 10 μM nigericin over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation. (E) Primary BMDMs were generated from WT and GSDMD knockout (GSDMD −/− ) C57BL/6 mice. BMDMs were then primed with LPS and stimulated with 10μM nigericin over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation. (F) Primary BMDMs were generated from WT and NLRP3 knockout (NLRP3 −/− ) C57BL/6 mice. BMDMs were then primed with LPS and stimulated with 10 μM nigericin over a time course of 45 min. Cellular lysates were examined by western blot for changes in signaling pathway phosphorylation. (G) iBMDMs were primed with LPS and stimulated with 10 μM nigericin or 10 μM rotenone over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation and GSDMD cleavage. (H) iBMDMs were primed with LPS and stimulated with 10 μM nigericin or 10 μM carbonyl cyanide- p -trifluoromethoxyphenylhydrazone (FCCP) over a time course of 45 min. Cellular lysates were examined by western blot for changes in ERK1/2 phosphorylation and GSDMD cleavage. All western blots are representative of at least three independent experiments.

Article Snippet: CL097 , MedChemExpress , Cat#: HY-128799.

Techniques: Western Blot, Knock-Out, Generated

Journal: Cell reports

Article Title: Restraint of inflammasome-driven cytokine responses through the mRNA stability protein TTP

doi: 10.1016/j.celrep.2025.115340

Figure Lengend Snippet:

Article Snippet: CL097 , MedChemExpress , Cat#: HY-128799.

Techniques: Recombinant, CyQUANT Assay, LDH Cytotoxicity Assay, Enzyme-linked Immunosorbent Assay, Software