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stx  (MedChemExpress)


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    Structured Review

    MedChemExpress stx
    Stx, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 93/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/stx/product/MedChemExpress
    Average 93 stars, based on 3 article reviews
    stx - by Bioz Stars, 2026-02
    93/100 stars

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    Millipore stx-0119
    Genetic and pharmacological STAT3 inhibition in glioma cells: ( A ) representative immunoblots of p-STAT3, STAT3, PML, SOX9, and SOX2 in U251-MG and GNS166 cells in STAT3 knockdown (“ sh41 ” and “ sh43 ”) and control (“ pLKO ”) cells ( n = 3); ( B ) quantification of cell growth in sh41 and sh43 cells compared with controls ( n = 2); ( C ) quantification of SA-β-gal + cells in STAT3 knockdown cells ( n = 2); ( D ) quantification of tumorspheres (primary and secondary) in sh41 and sh43 U251-MG cells relative to pLKO condition ( n = 2); ( E ) tumor volume representation at indicated time points after subcutaneous injection of U251-MG cells ( n = 4); ( F ) ELDA plot of limiting dilution assay of sh41, sh43 , and control U251-MG cells; ( G ) cytotoxicity exhibited by indicated glioma cells after treatment with increasing doses of <t>STX-0119</t> for 72 h ( n = 6); ( H ) quantification of tumorspheres in indicated cells after treatment with 50 and 100 µM STX-0119 ( n = 3). Calculations were relative to untreated cells; ( I ) representative immunoblot of p-STAT3, STAT3, PML, SOX9, and SOX2 expression in U251-MG cells after treatment with 50 and 100 µM STX-0119 for 72 h ( n = 3). * p < 0.05, ** p < 0.01, *** p < 0.001.
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    Genetic and pharmacological STAT3 inhibition in glioma cells: ( A ) representative immunoblots of p-STAT3, STAT3, PML, SOX9, and SOX2 in U251-MG and GNS166 cells in STAT3 knockdown (“ sh41 ” and “ sh43 ”) and control (“ pLKO ”) cells ( n = 3); ( B ) quantification of cell growth in sh41 and sh43 cells compared with controls ( n = 2); ( C ) quantification of SA-β-gal + cells in STAT3 knockdown cells ( n = 2); ( D ) quantification of tumorspheres (primary and secondary) in sh41 and sh43 U251-MG cells relative to pLKO condition ( n = 2); ( E ) tumor volume representation at indicated time points after subcutaneous injection of U251-MG cells ( n = 4); ( F ) ELDA plot of limiting dilution assay of sh41, sh43 , and control U251-MG cells; ( G ) cytotoxicity exhibited by indicated glioma cells after treatment with increasing doses of <t>STX-0119</t> for 72 h ( n = 6); ( H ) quantification of tumorspheres in indicated cells after treatment with 50 and 100 µM STX-0119 ( n = 3). Calculations were relative to untreated cells; ( I ) representative immunoblot of p-STAT3, STAT3, PML, SOX9, and SOX2 expression in U251-MG cells after treatment with 50 and 100 µM STX-0119 for 72 h ( n = 3). * p < 0.05, ** p < 0.01, *** p < 0.001.
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    Key Organics Inc UK stx- 0119
    Genetic and pharmacological STAT3 inhibition in glioma cells: ( A ) representative immunoblots of p-STAT3, STAT3, PML, SOX9, and SOX2 in U251-MG and GNS166 cells in STAT3 knockdown (“ sh41 ” and “ sh43 ”) and control (“ pLKO ”) cells ( n = 3); ( B ) quantification of cell growth in sh41 and sh43 cells compared with controls ( n = 2); ( C ) quantification of SA-β-gal + cells in STAT3 knockdown cells ( n = 2); ( D ) quantification of tumorspheres (primary and secondary) in sh41 and sh43 U251-MG cells relative to pLKO condition ( n = 2); ( E ) tumor volume representation at indicated time points after subcutaneous injection of U251-MG cells ( n = 4); ( F ) ELDA plot of limiting dilution assay of sh41, sh43 , and control U251-MG cells; ( G ) cytotoxicity exhibited by indicated glioma cells after treatment with increasing doses of <t>STX-0119</t> for 72 h ( n = 6); ( H ) quantification of tumorspheres in indicated cells after treatment with 50 and 100 µM STX-0119 ( n = 3). Calculations were relative to untreated cells; ( I ) representative immunoblot of p-STAT3, STAT3, PML, SOX9, and SOX2 expression in U251-MG cells after treatment with 50 and 100 µM STX-0119 for 72 h ( n = 3). * p < 0.05, ** p < 0.01, *** p < 0.001.
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    Genetic and pharmacological STAT3 inhibition in glioma cells: ( A ) representative immunoblots of p-STAT3, STAT3, PML, SOX9, and SOX2 in U251-MG and GNS166 cells in STAT3 knockdown (“ sh41 ” and “ sh43 ”) and control (“ pLKO ”) cells ( n = 3); ( B ) quantification of cell growth in sh41 and sh43 cells compared with controls ( n = 2); ( C ) quantification of SA-β-gal + cells in STAT3 knockdown cells ( n = 2); ( D ) quantification of tumorspheres (primary and secondary) in sh41 and sh43 U251-MG cells relative to pLKO condition ( n = 2); ( E ) tumor volume representation at indicated time points after subcutaneous injection of U251-MG cells ( n = 4); ( F ) ELDA plot of limiting dilution assay of sh41, sh43 , and control U251-MG cells; ( G ) cytotoxicity exhibited by indicated glioma cells after treatment with increasing doses of STX-0119 for 72 h ( n = 6); ( H ) quantification of tumorspheres in indicated cells after treatment with 50 and 100 µM STX-0119 ( n = 3). Calculations were relative to untreated cells; ( I ) representative immunoblot of p-STAT3, STAT3, PML, SOX9, and SOX2 expression in U251-MG cells after treatment with 50 and 100 µM STX-0119 for 72 h ( n = 3). * p < 0.05, ** p < 0.01, *** p < 0.001.

    Journal: International Journal of Molecular Sciences

    Article Title: High SOX9 Maintains Glioma Stem Cell Activity through a Regulatory Loop Involving STAT3 and PML

    doi: 10.3390/ijms23094511

    Figure Lengend Snippet: Genetic and pharmacological STAT3 inhibition in glioma cells: ( A ) representative immunoblots of p-STAT3, STAT3, PML, SOX9, and SOX2 in U251-MG and GNS166 cells in STAT3 knockdown (“ sh41 ” and “ sh43 ”) and control (“ pLKO ”) cells ( n = 3); ( B ) quantification of cell growth in sh41 and sh43 cells compared with controls ( n = 2); ( C ) quantification of SA-β-gal + cells in STAT3 knockdown cells ( n = 2); ( D ) quantification of tumorspheres (primary and secondary) in sh41 and sh43 U251-MG cells relative to pLKO condition ( n = 2); ( E ) tumor volume representation at indicated time points after subcutaneous injection of U251-MG cells ( n = 4); ( F ) ELDA plot of limiting dilution assay of sh41, sh43 , and control U251-MG cells; ( G ) cytotoxicity exhibited by indicated glioma cells after treatment with increasing doses of STX-0119 for 72 h ( n = 6); ( H ) quantification of tumorspheres in indicated cells after treatment with 50 and 100 µM STX-0119 ( n = 3). Calculations were relative to untreated cells; ( I ) representative immunoblot of p-STAT3, STAT3, PML, SOX9, and SOX2 expression in U251-MG cells after treatment with 50 and 100 µM STX-0119 for 72 h ( n = 3). * p < 0.05, ** p < 0.01, *** p < 0.001.

    Article Snippet: Cells were seeded in 96-well plates at a density of 2.5 × 10 3 cells per well and treated 24 h later with the indicated concentrations of STX-0119 (Sigma-Aldrich) for 72 h or arsenic trioxide (ATO; Sigma-Aldrich) for 48 h, in sextuplicates.

    Techniques: Inhibition, Western Blot, Injection, Limiting Dilution Assay, Expressing