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mtecs  (ATCC)


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    Structured Review

    ATCC mtecs
    ( A ) The thermal effect of LIPUS with different duty cycles on <t>MTECs.</t> ( B and C ) Flow cytometry of apoptosis of MTECs treated with LIPUS at varying duty cycles ( B ) and intensities ( C ) and quantification of apoptotic cells (Q2 + Q3). ( n = 3). ( D ) Protein levels of α-SMA in MTECs induced with 15 <t>ng/mL</t> <t>TGF-β1</t> ( n = 6). ( E ) Protein levels of α-SMA in MTECs treated with LIPUS at varying intensities ( n = 4). ( F ) Protein levels of α-SMA in MTECs treated with LIPUS at varying intensities stimulated by 15 ng/mL TGF-β1 ( n = 5). Data are presented as mean ± SD and were analyzed using 1-way ANOVA with Tukey’s post hoc test. * P < 0.05, ** P < 0.01, *** P < 0.001.
    Mtecs, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 224 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    mtecs - by Bioz Stars, 2026-03
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    Images

    1) Product Images from "Low-intensity pulsed ultrasound stimulation to treat renal fibrosis through inhibiting tubular IL-1R"

    Article Title: Low-intensity pulsed ultrasound stimulation to treat renal fibrosis through inhibiting tubular IL-1R

    Journal: JCI Insight

    doi: 10.1172/jci.insight.186892

    ( A ) The thermal effect of LIPUS with different duty cycles on MTECs. ( B and C ) Flow cytometry of apoptosis of MTECs treated with LIPUS at varying duty cycles ( B ) and intensities ( C ) and quantification of apoptotic cells (Q2 + Q3). ( n = 3). ( D ) Protein levels of α-SMA in MTECs induced with 15 ng/mL TGF-β1 ( n = 6). ( E ) Protein levels of α-SMA in MTECs treated with LIPUS at varying intensities ( n = 4). ( F ) Protein levels of α-SMA in MTECs treated with LIPUS at varying intensities stimulated by 15 ng/mL TGF-β1 ( n = 5). Data are presented as mean ± SD and were analyzed using 1-way ANOVA with Tukey’s post hoc test. * P < 0.05, ** P < 0.01, *** P < 0.001.
    Figure Legend Snippet: ( A ) The thermal effect of LIPUS with different duty cycles on MTECs. ( B and C ) Flow cytometry of apoptosis of MTECs treated with LIPUS at varying duty cycles ( B ) and intensities ( C ) and quantification of apoptotic cells (Q2 + Q3). ( n = 3). ( D ) Protein levels of α-SMA in MTECs induced with 15 ng/mL TGF-β1 ( n = 6). ( E ) Protein levels of α-SMA in MTECs treated with LIPUS at varying intensities ( n = 4). ( F ) Protein levels of α-SMA in MTECs treated with LIPUS at varying intensities stimulated by 15 ng/mL TGF-β1 ( n = 5). Data are presented as mean ± SD and were analyzed using 1-way ANOVA with Tukey’s post hoc test. * P < 0.05, ** P < 0.01, *** P < 0.001.

    Techniques Used: Flow Cytometry



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    ( A ) The thermal effect of LIPUS with different duty cycles on <t>MTECs.</t> ( B and C ) Flow cytometry of apoptosis of MTECs treated with LIPUS at varying duty cycles ( B ) and intensities ( C ) and quantification of apoptotic cells (Q2 + Q3). ( n = 3). ( D ) Protein levels of α-SMA in MTECs induced with 15 <t>ng/mL</t> <t>TGF-β1</t> ( n = 6). ( E ) Protein levels of α-SMA in MTECs treated with LIPUS at varying intensities ( n = 4). ( F ) Protein levels of α-SMA in MTECs treated with LIPUS at varying intensities stimulated by 15 ng/mL TGF-β1 ( n = 5). Data are presented as mean ± SD and were analyzed using 1-way ANOVA with Tukey’s post hoc test. * P < 0.05, ** P < 0.01, *** P < 0.001.
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    ( A ) The thermal effect of LIPUS with different duty cycles on <t>MTECs.</t> ( B and C ) Flow cytometry of apoptosis of MTECs treated with LIPUS at varying duty cycles ( B ) and intensities ( C ) and quantification of apoptotic cells (Q2 + Q3). ( n = 3). ( D ) Protein levels of α-SMA in MTECs induced with 15 <t>ng/mL</t> <t>TGF-β1</t> ( n = 6). ( E ) Protein levels of α-SMA in MTECs treated with LIPUS at varying intensities ( n = 4). ( F ) Protein levels of α-SMA in MTECs treated with LIPUS at varying intensities stimulated by 15 ng/mL TGF-β1 ( n = 5). Data are presented as mean ± SD and were analyzed using 1-way ANOVA with Tukey’s post hoc test. * P < 0.05, ** P < 0.01, *** P < 0.001.
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    ( A ) The thermal effect of LIPUS with different duty cycles on <t>MTECs.</t> ( B and C ) Flow cytometry of apoptosis of MTECs treated with LIPUS at varying duty cycles ( B ) and intensities ( C ) and quantification of apoptotic cells (Q2 + Q3). ( n = 3). ( D ) Protein levels of α-SMA in MTECs induced with 15 <t>ng/mL</t> <t>TGF-β1</t> ( n = 6). ( E ) Protein levels of α-SMA in MTECs treated with LIPUS at varying intensities ( n = 4). ( F ) Protein levels of α-SMA in MTECs treated with LIPUS at varying intensities stimulated by 15 ng/mL TGF-β1 ( n = 5). Data are presented as mean ± SD and were analyzed using 1-way ANOVA with Tukey’s post hoc test. * P < 0.05, ** P < 0.01, *** P < 0.001.
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    ( A ) The thermal effect of LIPUS with different duty cycles on <t>MTECs.</t> ( B and C ) Flow cytometry of apoptosis of MTECs treated with LIPUS at varying duty cycles ( B ) and intensities ( C ) and quantification of apoptotic cells (Q2 + Q3). ( n = 3). ( D ) Protein levels of α-SMA in MTECs induced with 15 <t>ng/mL</t> <t>TGF-β1</t> ( n = 6). ( E ) Protein levels of α-SMA in MTECs treated with LIPUS at varying intensities ( n = 4). ( F ) Protein levels of α-SMA in MTECs treated with LIPUS at varying intensities stimulated by 15 ng/mL TGF-β1 ( n = 5). Data are presented as mean ± SD and were analyzed using 1-way ANOVA with Tukey’s post hoc test. * P < 0.05, ** P < 0.01, *** P < 0.001.
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    ( A ) The thermal effect of LIPUS with different duty cycles on <t>MTECs.</t> ( B and C ) Flow cytometry of apoptosis of MTECs treated with LIPUS at varying duty cycles ( B ) and intensities ( C ) and quantification of apoptotic cells (Q2 + Q3). ( n = 3). ( D ) Protein levels of α-SMA in MTECs induced with 15 <t>ng/mL</t> <t>TGF-β1</t> ( n = 6). ( E ) Protein levels of α-SMA in MTECs treated with LIPUS at varying intensities ( n = 4). ( F ) Protein levels of α-SMA in MTECs treated with LIPUS at varying intensities stimulated by 15 ng/mL TGF-β1 ( n = 5). Data are presented as mean ± SD and were analyzed using 1-way ANOVA with Tukey’s post hoc test. * P < 0.05, ** P < 0.01, *** P < 0.001.
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    ( A ) The thermal effect of LIPUS with different duty cycles on <t>MTECs.</t> ( B and C ) Flow cytometry of apoptosis of MTECs treated with LIPUS at varying duty cycles ( B ) and intensities ( C ) and quantification of apoptotic cells (Q2 + Q3). ( n = 3). ( D ) Protein levels of α-SMA in MTECs induced with 15 <t>ng/mL</t> <t>TGF-β1</t> ( n = 6). ( E ) Protein levels of α-SMA in MTECs treated with LIPUS at varying intensities ( n = 4). ( F ) Protein levels of α-SMA in MTECs treated with LIPUS at varying intensities stimulated by 15 ng/mL TGF-β1 ( n = 5). Data are presented as mean ± SD and were analyzed using 1-way ANOVA with Tukey’s post hoc test. * P < 0.05, ** P < 0.01, *** P < 0.001.
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    Results from indole testing for confirmation of E. coli in isolates preserved from plates and IDEXX trays.
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    Image Search Results


    ( A ) The thermal effect of LIPUS with different duty cycles on MTECs. ( B and C ) Flow cytometry of apoptosis of MTECs treated with LIPUS at varying duty cycles ( B ) and intensities ( C ) and quantification of apoptotic cells (Q2 + Q3). ( n = 3). ( D ) Protein levels of α-SMA in MTECs induced with 15 ng/mL TGF-β1 ( n = 6). ( E ) Protein levels of α-SMA in MTECs treated with LIPUS at varying intensities ( n = 4). ( F ) Protein levels of α-SMA in MTECs treated with LIPUS at varying intensities stimulated by 15 ng/mL TGF-β1 ( n = 5). Data are presented as mean ± SD and were analyzed using 1-way ANOVA with Tukey’s post hoc test. * P < 0.05, ** P < 0.01, *** P < 0.001.

    Journal: JCI Insight

    Article Title: Low-intensity pulsed ultrasound stimulation to treat renal fibrosis through inhibiting tubular IL-1R

    doi: 10.1172/jci.insight.186892

    Figure Lengend Snippet: ( A ) The thermal effect of LIPUS with different duty cycles on MTECs. ( B and C ) Flow cytometry of apoptosis of MTECs treated with LIPUS at varying duty cycles ( B ) and intensities ( C ) and quantification of apoptotic cells (Q2 + Q3). ( n = 3). ( D ) Protein levels of α-SMA in MTECs induced with 15 ng/mL TGF-β1 ( n = 6). ( E ) Protein levels of α-SMA in MTECs treated with LIPUS at varying intensities ( n = 4). ( F ) Protein levels of α-SMA in MTECs treated with LIPUS at varying intensities stimulated by 15 ng/mL TGF-β1 ( n = 5). Data are presented as mean ± SD and were analyzed using 1-way ANOVA with Tukey’s post hoc test. * P < 0.05, ** P < 0.01, *** P < 0.001.

    Article Snippet: Following serum starvation, MTECs (catalog CCL-139, ATCC) were exposed to recombinant human TGF-β1 (catalog AF-100-21C, Peprotech) at 15 ng/mL or rIL-1β at 5, 10, and 20 pg/μL.

    Techniques: Flow Cytometry

    Results from indole testing for confirmation of E. coli in isolates preserved from plates and IDEXX trays.

    Journal: One Health

    Article Title: Evaluation of a modified IDEXX method for antimicrobial resistance monitoring of extended Beta-lactamases-producing Escherichia coli in impacted waters near the U.S.-Mexico border

    doi: 10.1016/j.onehlt.2025.100997

    Figure Lengend Snippet: Results from indole testing for confirmation of E. coli in isolates preserved from plates and IDEXX trays.

    Article Snippet: Each water sample was analyzed for ESBL-Ec by three methods: traditional membrane filtration with mTEC agar, traditional membrane filtration with TBX, and the modified IDEXX-based method ( ).

    Techniques:

    Correlation graphs for detection of E. coli (top) and ESBL-Ec (bottom) for samples from Imperial Beach and the Tijuana River. The modified IDEXX method correlated with membrane filtration methods using selective mTEC (r = 0.965, p < 0.001, n = 14) and TBX (r = 0.95, p < 0.001, n = 14) agars. Comparatively, the IDEXX method correlated with membrane filtration methods using selective mTEC (r = 0.978, p < 0.001, n = 10) and TBX (r = 0.975, p < 0.001, n = 10) agars.

    Journal: One Health

    Article Title: Evaluation of a modified IDEXX method for antimicrobial resistance monitoring of extended Beta-lactamases-producing Escherichia coli in impacted waters near the U.S.-Mexico border

    doi: 10.1016/j.onehlt.2025.100997

    Figure Lengend Snippet: Correlation graphs for detection of E. coli (top) and ESBL-Ec (bottom) for samples from Imperial Beach and the Tijuana River. The modified IDEXX method correlated with membrane filtration methods using selective mTEC (r = 0.965, p < 0.001, n = 14) and TBX (r = 0.95, p < 0.001, n = 14) agars. Comparatively, the IDEXX method correlated with membrane filtration methods using selective mTEC (r = 0.978, p < 0.001, n = 10) and TBX (r = 0.975, p < 0.001, n = 10) agars.

    Article Snippet: Each water sample was analyzed for ESBL-Ec by three methods: traditional membrane filtration with mTEC agar, traditional membrane filtration with TBX, and the modified IDEXX-based method ( ).

    Techniques: Modification, Membrane, Filtration

    Cost Comparison for 10 sites using different methods.

    Journal: One Health

    Article Title: Evaluation of a modified IDEXX method for antimicrobial resistance monitoring of extended Beta-lactamases-producing Escherichia coli in impacted waters near the U.S.-Mexico border

    doi: 10.1016/j.onehlt.2025.100997

    Figure Lengend Snippet: Cost Comparison for 10 sites using different methods.

    Article Snippet: Each water sample was analyzed for ESBL-Ec by three methods: traditional membrane filtration with mTEC agar, traditional membrane filtration with TBX, and the modified IDEXX-based method ( ).

    Techniques: Comparison, Filtration