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multi-function microplate reader tecan infinite® 200 pro  (Tecan Systems)


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    Tecan Systems multi-function microplate reader tecan infinite® 200 pro
    Multi Function Microplate Reader Tecan Infinite® 200 Pro, supplied by Tecan Systems, 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/multi-function microplate reader tecan infinite® 200 pro/product/Tecan Systems
    Average 90 stars, based on 1 article reviews
    multi-function microplate reader tecan infinite® 200 pro - by Bioz Stars, 2026-04
    90/100 stars

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    Tecan Systems 3001 multi function microplate reader
    ROS accumulation in HGC-27 and MFC cells is induced by luteolin. The fluorescence intensity of (A) HGC-27 cells and (B) MFC cells were visualized under a fluorescence inverted microscope (magnification, ×100). Luteolin-induced ROS levels were detected using DCFH-DA staining and flow cytometry in (C) HGC-27 cells and (E) MFC cells. The quantitative analysis of ROS levels in (D) HGC-27 cells and (F) MFC cells was showed on the histogram. (G) SOD activity was assessed in HGC-27 and MFC cells using a <t>microplate</t> reader at an absorbance of 560 nm. Experiments were repeated at least in triplicate. Data were presented as mean ± SD. **P<0.01 vs. DMSO group. ROS, reactive oxygen species; SOD, superoxide dismutase; HGC-27, human gastric cancer HGC-27 cell line; MFC, mouse forestomach carcinoma cell line.
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    ROS accumulation in HGC-27 and MFC cells is induced by luteolin. The fluorescence intensity of (A) HGC-27 cells and (B) MFC cells were visualized under a fluorescence inverted microscope (magnification, ×100). Luteolin-induced ROS levels were detected using DCFH-DA staining and flow cytometry in (C) HGC-27 cells and (E) MFC cells. The quantitative analysis of ROS levels in (D) HGC-27 cells and (F) MFC cells was showed on the histogram. (G) SOD activity was assessed in HGC-27 and MFC cells using a microplate reader at an absorbance of 560 nm. Experiments were repeated at least in triplicate. Data were presented as mean ± SD. **P<0.01 vs. DMSO group. ROS, reactive oxygen species; SOD, superoxide dismutase; HGC-27, human gastric cancer HGC-27 cell line; MFC, mouse forestomach carcinoma cell line.

    Journal: Oncology Letters

    Article Title: Luteolin induces apoptosis by impairing mitochondrial function and targeting the intrinsic apoptosis pathway in gastric cancer cells

    doi: 10.3892/ol.2023.13913

    Figure Lengend Snippet: ROS accumulation in HGC-27 and MFC cells is induced by luteolin. The fluorescence intensity of (A) HGC-27 cells and (B) MFC cells were visualized under a fluorescence inverted microscope (magnification, ×100). Luteolin-induced ROS levels were detected using DCFH-DA staining and flow cytometry in (C) HGC-27 cells and (E) MFC cells. The quantitative analysis of ROS levels in (D) HGC-27 cells and (F) MFC cells was showed on the histogram. (G) SOD activity was assessed in HGC-27 and MFC cells using a microplate reader at an absorbance of 560 nm. Experiments were repeated at least in triplicate. Data were presented as mean ± SD. **P<0.01 vs. DMSO group. ROS, reactive oxygen species; SOD, superoxide dismutase; HGC-27, human gastric cancer HGC-27 cell line; MFC, mouse forestomach carcinoma cell line.

    Article Snippet: After incubation at 37°C for 60 min in the dark, the absorbance at a wavelength of 450 nm was detected using a Thermo 3001 multi-function microplate reader (Infinite 200 PRO, Tecan Austria GmbH, Salzburg, Austria).

    Techniques: Fluorescence, Inverted Microscopy, Staining, Flow Cytometry, Activity Assay

    Mitochondrial membrane potential, ATP levels and some enzyme activities in HGC-27 and MFC cells induced by luteolin. The luteolin-treated (A) HGC-27 cells and (C) MFC cells were stained with JC-1, and analyzed using flow cytometry. Quantitative statistics of the mitochondrial membrane potential was based on flow cytometry in (B) HGC-27 cells and (D) MFC cells. The (E) ATP levels, (F) Na + /K + -ATPase activities and (G) Ca 2+ /Mg 2+ -ATPase activities were showed based on the microplate system at the absorbance values of 660 nm. The data were presented as mean ± SD. The experiments were repeated in triplicate. *P<0.05, **P<0.01 vs. DMSO group. HGC-27, human gastric cancer HGC-27 cell line; MFC, mouse forestomach carcinoma cell line.

    Journal: Oncology Letters

    Article Title: Luteolin induces apoptosis by impairing mitochondrial function and targeting the intrinsic apoptosis pathway in gastric cancer cells

    doi: 10.3892/ol.2023.13913

    Figure Lengend Snippet: Mitochondrial membrane potential, ATP levels and some enzyme activities in HGC-27 and MFC cells induced by luteolin. The luteolin-treated (A) HGC-27 cells and (C) MFC cells were stained with JC-1, and analyzed using flow cytometry. Quantitative statistics of the mitochondrial membrane potential was based on flow cytometry in (B) HGC-27 cells and (D) MFC cells. The (E) ATP levels, (F) Na + /K + -ATPase activities and (G) Ca 2+ /Mg 2+ -ATPase activities were showed based on the microplate system at the absorbance values of 660 nm. The data were presented as mean ± SD. The experiments were repeated in triplicate. *P<0.05, **P<0.01 vs. DMSO group. HGC-27, human gastric cancer HGC-27 cell line; MFC, mouse forestomach carcinoma cell line.

    Article Snippet: After incubation at 37°C for 60 min in the dark, the absorbance at a wavelength of 450 nm was detected using a Thermo 3001 multi-function microplate reader (Infinite 200 PRO, Tecan Austria GmbH, Salzburg, Austria).

    Techniques: Membrane, Staining, Flow Cytometry

    Luteolin induces the enzyme activities of the METC complexes in HGC-27 and MFC cells. Complexes (A) I, (B) III and (C) V were assessed by testing kits. The data were obtained using a microplate reader at 340, 550 and 660 nm, respectively. The data were presented as mean ± SD. The experiments were performed at least in triplicate. *P<0.05 and **P<0.01 vs. DMSO group; HGC-27, human gastric cancer HGC-27 cell line; MFC, mouse forestomach carcinoma cell line.

    Journal: Oncology Letters

    Article Title: Luteolin induces apoptosis by impairing mitochondrial function and targeting the intrinsic apoptosis pathway in gastric cancer cells

    doi: 10.3892/ol.2023.13913

    Figure Lengend Snippet: Luteolin induces the enzyme activities of the METC complexes in HGC-27 and MFC cells. Complexes (A) I, (B) III and (C) V were assessed by testing kits. The data were obtained using a microplate reader at 340, 550 and 660 nm, respectively. The data were presented as mean ± SD. The experiments were performed at least in triplicate. *P<0.05 and **P<0.01 vs. DMSO group; HGC-27, human gastric cancer HGC-27 cell line; MFC, mouse forestomach carcinoma cell line.

    Article Snippet: After incubation at 37°C for 60 min in the dark, the absorbance at a wavelength of 450 nm was detected using a Thermo 3001 multi-function microplate reader (Infinite 200 PRO, Tecan Austria GmbH, Salzburg, Austria).

    Techniques: