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nbqx  (Alomone Labs)


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    Structured Review

    Alomone Labs nbqx
    Nbqx, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 27 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/n-185/pmc12834114-2-0-2?v=Alomone+Labs
    Average 94 stars, based on 27 article reviews
    nbqx - by Bioz Stars, 2026-07
    94/100 stars

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    n a549  (ATCC)
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    ATCC n a549
    Quantification of reactive oxygen species (ROS) induced by blue light irradiation. <t>A549</t> cells were pretreated for 1 h with the indicated concentrations of Ir­(III) complexes. Cells were then irradiated for 1 h with blue light. Intracellular ROS were quantified using the CellRox Green probe and analyzed via flow cytometry. ROS levels are normalized to irradiated, untreated control samples. Data represent the mean ± standard deviation from three independent experiments, with duplicate samples in each run.
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    Quantification of reactive oxygen species (ROS) induced by blue light irradiation. <t>A549</t> cells were pretreated for 1 h with the indicated concentrations of Ir­(III) complexes. Cells were then irradiated for 1 h with blue light. Intracellular ROS were quantified using the CellRox Green probe and analyzed via flow cytometry. ROS levels are normalized to irradiated, untreated control samples. Data represent the mean ± standard deviation from three independent experiments, with duplicate samples in each run.
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    ATCC paper n a a549 ruvbl2 ko
    Quantification of reactive oxygen species (ROS) induced by blue light irradiation. <t>A549</t> cells were pretreated for 1 h with the indicated concentrations of Ir­(III) complexes. Cells were then irradiated for 1 h with blue light. Intracellular ROS were quantified using the CellRox Green probe and analyzed via flow cytometry. ROS levels are normalized to irradiated, untreated control samples. Data represent the mean ± standard deviation from three independent experiments, with duplicate samples in each run.
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    Quantification of reactive oxygen species (ROS) induced by blue light irradiation. <t>A549</t> cells were pretreated for 1 h with the indicated concentrations of Ir­(III) complexes. Cells were then irradiated for 1 h with blue light. Intracellular ROS were quantified using the CellRox Green probe and analyzed via flow cytometry. ROS levels are normalized to irradiated, untreated control samples. Data represent the mean ± standard deviation from three independent experiments, with duplicate samples in each run.
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    Quantification of reactive oxygen species (ROS) induced by blue light irradiation. <t>A549</t> cells were pretreated for 1 h with the indicated concentrations of Ir­(III) complexes. Cells were then irradiated for 1 h with blue light. Intracellular ROS were quantified using the CellRox Green probe and analyzed via flow cytometry. ROS levels are normalized to irradiated, untreated control samples. Data represent the mean ± standard deviation from three independent experiments, with duplicate samples in each run.
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    ATCC paper n a usp39 ko a549 cells
    Quantification of reactive oxygen species (ROS) induced by blue light irradiation. <t>A549</t> cells were pretreated for 1 h with the indicated concentrations of Ir­(III) complexes. Cells were then irradiated for 1 h with blue light. Intracellular ROS were quantified using the CellRox Green probe and analyzed via flow cytometry. ROS levels are normalized to irradiated, untreated control samples. Data represent the mean ± standard deviation from three independent experiments, with duplicate samples in each run.
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    Quantification of reactive oxygen species (ROS) induced by blue light irradiation. <t>A549</t> cells were pretreated for 1 h with the indicated concentrations of Ir­(III) complexes. Cells were then irradiated for 1 h with blue light. Intracellular ROS were quantified using the CellRox Green probe and analyzed via flow cytometry. ROS levels are normalized to irradiated, untreated control samples. Data represent the mean ± standard deviation from three independent experiments, with duplicate samples in each run.
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    ATCC paper n a a549 atcc
    Quantification of reactive oxygen species (ROS) induced by blue light irradiation. <t>A549</t> cells were pretreated for 1 h with the indicated concentrations of Ir­(III) complexes. Cells were then irradiated for 1 h with blue light. Intracellular ROS were quantified using the CellRox Green probe and analyzed via flow cytometry. ROS levels are normalized to irradiated, untreated control samples. Data represent the mean ± standard deviation from three independent experiments, with duplicate samples in each run.
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    Quantification of reactive oxygen species (ROS) induced by blue light irradiation. A549 cells were pretreated for 1 h with the indicated concentrations of Ir­(III) complexes. Cells were then irradiated for 1 h with blue light. Intracellular ROS were quantified using the CellRox Green probe and analyzed via flow cytometry. ROS levels are normalized to irradiated, untreated control samples. Data represent the mean ± standard deviation from three independent experiments, with duplicate samples in each run.

    Journal: Journal of Medicinal Chemistry

    Article Title: Novel 2‑(2′-Benzothiazolyl)-benzimidazole-Based Iridium(III) Photocatalysts Exhibit Antiproliferative Effects in 2D and 3D Cancer Cells to Bypass Hypoxia-Induced Resistance

    doi: 10.1021/acs.jmedchem.5c03280

    Figure Lengend Snippet: Quantification of reactive oxygen species (ROS) induced by blue light irradiation. A549 cells were pretreated for 1 h with the indicated concentrations of Ir­(III) complexes. Cells were then irradiated for 1 h with blue light. Intracellular ROS were quantified using the CellRox Green probe and analyzed via flow cytometry. ROS levels are normalized to irradiated, untreated control samples. Data represent the mean ± standard deviation from three independent experiments, with duplicate samples in each run.

    Article Snippet: Elemental analysis (C, H, N, and S) of the ancillary ligand and the iridium (III) complexes was conducted in a TruSpec Leco microanalyzer equipped with nondispersive IR detectors for C, H, and S, and a thermal conductivity detector for N. A549 and HCC827 lung adenocarcinoma cell lines were from ATCC and colon carcinoma HCT-116 cells were from ECACC.

    Techniques: Irradiation, Flow Cytometry, Control, Standard Deviation

    Intracellular colocalization studies of iridium complexes 4 and 5 in A549 cells. A549 cells were incubated with 5 μM iridium complexes for 2 h, followed by costaining with specific cell trackers for mitochondria, endoplasmic reticulum, and lysosomes. Confocal microscopy was used for imaging. Scale bars represent 20 μm.

    Journal: Journal of Medicinal Chemistry

    Article Title: Novel 2‑(2′-Benzothiazolyl)-benzimidazole-Based Iridium(III) Photocatalysts Exhibit Antiproliferative Effects in 2D and 3D Cancer Cells to Bypass Hypoxia-Induced Resistance

    doi: 10.1021/acs.jmedchem.5c03280

    Figure Lengend Snippet: Intracellular colocalization studies of iridium complexes 4 and 5 in A549 cells. A549 cells were incubated with 5 μM iridium complexes for 2 h, followed by costaining with specific cell trackers for mitochondria, endoplasmic reticulum, and lysosomes. Confocal microscopy was used for imaging. Scale bars represent 20 μm.

    Article Snippet: Elemental analysis (C, H, N, and S) of the ancillary ligand and the iridium (III) complexes was conducted in a TruSpec Leco microanalyzer equipped with nondispersive IR detectors for C, H, and S, and a thermal conductivity detector for N. A549 and HCC827 lung adenocarcinoma cell lines were from ATCC and colon carcinoma HCT-116 cells were from ECACC.

    Techniques: Incubation, Confocal Microscopy, Imaging

    Intracellular NADH depletion in A549 cells. A549 cells were treated with the respective complexes at their IC 50 concentrations for 2 h (1 h incubation in the dark followed by 1 h irradiation with blue light, 420 nm, 58 W/m 2 ). Experiments were performed in duplicate with triplicate samples per condition. Data are shown as mean ± SD. Statistical significance between dark-incubated and irradiated samples was assessed using a two-tailed t test. Significance levels are indicated as follows: * P ≤ 0.05, ** P ≤ 0.01; “ns” denotes a nonsignificant difference.

    Journal: Journal of Medicinal Chemistry

    Article Title: Novel 2‑(2′-Benzothiazolyl)-benzimidazole-Based Iridium(III) Photocatalysts Exhibit Antiproliferative Effects in 2D and 3D Cancer Cells to Bypass Hypoxia-Induced Resistance

    doi: 10.1021/acs.jmedchem.5c03280

    Figure Lengend Snippet: Intracellular NADH depletion in A549 cells. A549 cells were treated with the respective complexes at their IC 50 concentrations for 2 h (1 h incubation in the dark followed by 1 h irradiation with blue light, 420 nm, 58 W/m 2 ). Experiments were performed in duplicate with triplicate samples per condition. Data are shown as mean ± SD. Statistical significance between dark-incubated and irradiated samples was assessed using a two-tailed t test. Significance levels are indicated as follows: * P ≤ 0.05, ** P ≤ 0.01; “ns” denotes a nonsignificant difference.

    Article Snippet: Elemental analysis (C, H, N, and S) of the ancillary ligand and the iridium (III) complexes was conducted in a TruSpec Leco microanalyzer equipped with nondispersive IR detectors for C, H, and S, and a thermal conductivity detector for N. A549 and HCC827 lung adenocarcinoma cell lines were from ATCC and colon carcinoma HCT-116 cells were from ECACC.

    Techniques: Incubation, Irradiation, Two Tailed Test