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fluorescence ubiquitination based cell cycle indicator fucci vsv g  (ATCC)


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    ATCC fluorescence ubiquitination based cell cycle indicator fucci vsv g
    Detroit 562 cells arrested in the G2 phase are susceptible to cell death. (A) Examination of the cell cycle in response to 24a treatment. Cell cycle distribution was determined by flow cytometric analysis of PI-stained cells following 24-h treatment at the indicated doses. GM04390 is normal human fibroblasts. Values represent the mean of n=2. (B) Examination of real-time cell cycle progression using FastFUCCI-expressing Detroit 562 cells. A fusion protein of Cdt1 and monomeric Kusabira Orange 2 creates the <t>FUCCI</t> reporter that allows visualization of cells in the G1 phase. A fusion of geminin with monomeric Azami Green allows for the monitoring of cells in the G2 phase. Cells were treated with 0.03 µM 24a for the indicated duration and PI was added 1 h prior to imaging. As shown circled, only cells arrested in the G2 phase also stained for PI. Magnification, ×20. (C) Assessment of compound binding by isothermal titration calorimetry. Random, fragmented DNA was titrated into a sample of buffer, 60 µM EtBr or 100 µM 24a. Raw heat values without further deconvolution are demonstrated. PI, propidium iodide; EtBr, ethidium bromide; FUCCI, <t>fluorescence</t> ubiquitination-based cell cycle indicator.
    Fluorescence Ubiquitination Based Cell Cycle Indicator Fucci Vsv G, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 433 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fluorescence+ubiquitination+based+cell+cycle+indicator+fucci+vsv+g/Vesicular+stomatitis+virus/pmc08923654-72-6-24
    Average 94 stars, based on 433 article reviews
    fluorescence ubiquitination based cell cycle indicator fucci vsv g - by Bioz Stars, 2026-09
    94/100 stars

    Images

    1) Product Images from "Discovery of a potent cytotoxic agent that promotes G 2 /M phase cell cycle arrest and apoptosis in a malignant human pharyngeal squamous carcinoma cell line"

    Article Title: Discovery of a potent cytotoxic agent that promotes G 2 /M phase cell cycle arrest and apoptosis in a malignant human pharyngeal squamous carcinoma cell line

    Journal: International Journal of Oncology

    doi: 10.3892/ijo.2022.5331

    Detroit 562 cells arrested in the G2 phase are susceptible to cell death. (A) Examination of the cell cycle in response to 24a treatment. Cell cycle distribution was determined by flow cytometric analysis of PI-stained cells following 24-h treatment at the indicated doses. GM04390 is normal human fibroblasts. Values represent the mean of n=2. (B) Examination of real-time cell cycle progression using FastFUCCI-expressing Detroit 562 cells. A fusion protein of Cdt1 and monomeric Kusabira Orange 2 creates the FUCCI reporter that allows visualization of cells in the G1 phase. A fusion of geminin with monomeric Azami Green allows for the monitoring of cells in the G2 phase. Cells were treated with 0.03 µM 24a for the indicated duration and PI was added 1 h prior to imaging. As shown circled, only cells arrested in the G2 phase also stained for PI. Magnification, ×20. (C) Assessment of compound binding by isothermal titration calorimetry. Random, fragmented DNA was titrated into a sample of buffer, 60 µM EtBr or 100 µM 24a. Raw heat values without further deconvolution are demonstrated. PI, propidium iodide; EtBr, ethidium bromide; FUCCI, fluorescence ubiquitination-based cell cycle indicator.
    Figure Legend Snippet: Detroit 562 cells arrested in the G2 phase are susceptible to cell death. (A) Examination of the cell cycle in response to 24a treatment. Cell cycle distribution was determined by flow cytometric analysis of PI-stained cells following 24-h treatment at the indicated doses. GM04390 is normal human fibroblasts. Values represent the mean of n=2. (B) Examination of real-time cell cycle progression using FastFUCCI-expressing Detroit 562 cells. A fusion protein of Cdt1 and monomeric Kusabira Orange 2 creates the FUCCI reporter that allows visualization of cells in the G1 phase. A fusion of geminin with monomeric Azami Green allows for the monitoring of cells in the G2 phase. Cells were treated with 0.03 µM 24a for the indicated duration and PI was added 1 h prior to imaging. As shown circled, only cells arrested in the G2 phase also stained for PI. Magnification, ×20. (C) Assessment of compound binding by isothermal titration calorimetry. Random, fragmented DNA was titrated into a sample of buffer, 60 µM EtBr or 100 µM 24a. Raw heat values without further deconvolution are demonstrated. PI, propidium iodide; EtBr, ethidium bromide; FUCCI, fluorescence ubiquitination-based cell cycle indicator.

    Techniques Used: Staining, Expressing, Imaging, Binding Assay, Isothermal Titration Calorimetry, Fluorescence, Ubiquitin Proteomics

    Related Articles

    Expressing:

    Article Title: Discovery of a potent cytotoxic agent that promotes G 2 /M phase cell cycle arrest and apoptosis in a malignant human pharyngeal squamous carcinoma cell line
    Article Snippet: The cell cycle distribution was determined with the NovoExpress software version 1.3.0 (ACEA Bioscience, Inc.). .. Construction of Detroit 562 cells expressing fluorescence ubiquitination-based cell cycle indicator (FUCCI) VSV-G pseudotyped lentiviral particles were generated from the transfection of 293T cells (ATCC) by the Lipofectamine ® 3000 reagent (Invitrogen; Thermo Fisher Scientific, Inc.) according to the manufacturer's recommendation with the 3rd generation pBOB-EF1-FastFUCCI-Puro transfer vector (plasmid no. 86849), the 2nd generation packaging plasmid pCMV-dR8.2 dpr (plasmid no. 8455) and the 2nd generation envelope plasmid pCMV-VSV-G (plasmid no. 8454) obtained from Addgene, Inc. 293T cells (at ~95% confluence in a 10-cm dish) were transfected with 10 μ g transfer vector, 5 μ g packaging plasmid and 5 μ g envelope plasmid and the media harvested 48 and 72 h post-transfection. ..

    Fluorescence:

    Article Title: Discovery of a potent cytotoxic agent that promotes G 2 /M phase cell cycle arrest and apoptosis in a malignant human pharyngeal squamous carcinoma cell line
    Article Snippet: The cell cycle distribution was determined with the NovoExpress software version 1.3.0 (ACEA Bioscience, Inc.). .. Construction of Detroit 562 cells expressing fluorescence ubiquitination-based cell cycle indicator (FUCCI) VSV-G pseudotyped lentiviral particles were generated from the transfection of 293T cells (ATCC) by the Lipofectamine ® 3000 reagent (Invitrogen; Thermo Fisher Scientific, Inc.) according to the manufacturer's recommendation with the 3rd generation pBOB-EF1-FastFUCCI-Puro transfer vector (plasmid no. 86849), the 2nd generation packaging plasmid pCMV-dR8.2 dpr (plasmid no. 8455) and the 2nd generation envelope plasmid pCMV-VSV-G (plasmid no. 8454) obtained from Addgene, Inc. 293T cells (at ~95% confluence in a 10-cm dish) were transfected with 10 μ g transfer vector, 5 μ g packaging plasmid and 5 μ g envelope plasmid and the media harvested 48 and 72 h post-transfection. ..

    Ubiquitin Proteomics:

    Article Title: Discovery of a potent cytotoxic agent that promotes G 2 /M phase cell cycle arrest and apoptosis in a malignant human pharyngeal squamous carcinoma cell line
    Article Snippet: The cell cycle distribution was determined with the NovoExpress software version 1.3.0 (ACEA Bioscience, Inc.). .. Construction of Detroit 562 cells expressing fluorescence ubiquitination-based cell cycle indicator (FUCCI) VSV-G pseudotyped lentiviral particles were generated from the transfection of 293T cells (ATCC) by the Lipofectamine ® 3000 reagent (Invitrogen; Thermo Fisher Scientific, Inc.) according to the manufacturer's recommendation with the 3rd generation pBOB-EF1-FastFUCCI-Puro transfer vector (plasmid no. 86849), the 2nd generation packaging plasmid pCMV-dR8.2 dpr (plasmid no. 8455) and the 2nd generation envelope plasmid pCMV-VSV-G (plasmid no. 8454) obtained from Addgene, Inc. 293T cells (at ~95% confluence in a 10-cm dish) were transfected with 10 μ g transfer vector, 5 μ g packaging plasmid and 5 μ g envelope plasmid and the media harvested 48 and 72 h post-transfection. ..

    Generated:

    Article Title: Discovery of a potent cytotoxic agent that promotes G 2 /M phase cell cycle arrest and apoptosis in a malignant human pharyngeal squamous carcinoma cell line
    Article Snippet: The cell cycle distribution was determined with the NovoExpress software version 1.3.0 (ACEA Bioscience, Inc.). .. Construction of Detroit 562 cells expressing fluorescence ubiquitination-based cell cycle indicator (FUCCI) VSV-G pseudotyped lentiviral particles were generated from the transfection of 293T cells (ATCC) by the Lipofectamine ® 3000 reagent (Invitrogen; Thermo Fisher Scientific, Inc.) according to the manufacturer's recommendation with the 3rd generation pBOB-EF1-FastFUCCI-Puro transfer vector (plasmid no. 86849), the 2nd generation packaging plasmid pCMV-dR8.2 dpr (plasmid no. 8455) and the 2nd generation envelope plasmid pCMV-VSV-G (plasmid no. 8454) obtained from Addgene, Inc. 293T cells (at ~95% confluence in a 10-cm dish) were transfected with 10 μ g transfer vector, 5 μ g packaging plasmid and 5 μ g envelope plasmid and the media harvested 48 and 72 h post-transfection. ..

    Transfection:

    Article Title: Discovery of a potent cytotoxic agent that promotes G 2 /M phase cell cycle arrest and apoptosis in a malignant human pharyngeal squamous carcinoma cell line
    Article Snippet: The cell cycle distribution was determined with the NovoExpress software version 1.3.0 (ACEA Bioscience, Inc.). .. Construction of Detroit 562 cells expressing fluorescence ubiquitination-based cell cycle indicator (FUCCI) VSV-G pseudotyped lentiviral particles were generated from the transfection of 293T cells (ATCC) by the Lipofectamine ® 3000 reagent (Invitrogen; Thermo Fisher Scientific, Inc.) according to the manufacturer's recommendation with the 3rd generation pBOB-EF1-FastFUCCI-Puro transfer vector (plasmid no. 86849), the 2nd generation packaging plasmid pCMV-dR8.2 dpr (plasmid no. 8455) and the 2nd generation envelope plasmid pCMV-VSV-G (plasmid no. 8454) obtained from Addgene, Inc. 293T cells (at ~95% confluence in a 10-cm dish) were transfected with 10 μ g transfer vector, 5 μ g packaging plasmid and 5 μ g envelope plasmid and the media harvested 48 and 72 h post-transfection. ..

    Plasmid Preparation:

    Article Title: Discovery of a potent cytotoxic agent that promotes G 2 /M phase cell cycle arrest and apoptosis in a malignant human pharyngeal squamous carcinoma cell line
    Article Snippet: The cell cycle distribution was determined with the NovoExpress software version 1.3.0 (ACEA Bioscience, Inc.). .. Construction of Detroit 562 cells expressing fluorescence ubiquitination-based cell cycle indicator (FUCCI) VSV-G pseudotyped lentiviral particles were generated from the transfection of 293T cells (ATCC) by the Lipofectamine ® 3000 reagent (Invitrogen; Thermo Fisher Scientific, Inc.) according to the manufacturer's recommendation with the 3rd generation pBOB-EF1-FastFUCCI-Puro transfer vector (plasmid no. 86849), the 2nd generation packaging plasmid pCMV-dR8.2 dpr (plasmid no. 8455) and the 2nd generation envelope plasmid pCMV-VSV-G (plasmid no. 8454) obtained from Addgene, Inc. 293T cells (at ~95% confluence in a 10-cm dish) were transfected with 10 μ g transfer vector, 5 μ g packaging plasmid and 5 μ g envelope plasmid and the media harvested 48 and 72 h post-transfection. ..



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    fluorescence ubiquitination based cell cycle indicator fucci vsv g  (ATCC)
    94
    ATCC fluorescence ubiquitination based cell cycle indicator fucci vsv g
    Detroit 562 cells arrested in the G2 phase are susceptible to cell death. (A) Examination of the cell cycle in response to 24a treatment. Cell cycle distribution was determined by flow cytometric analysis of PI-stained cells following 24-h treatment at the indicated doses. GM04390 is normal human fibroblasts. Values represent the mean of n=2. (B) Examination of real-time cell cycle progression using FastFUCCI-expressing Detroit 562 cells. A fusion protein of Cdt1 and monomeric Kusabira Orange 2 creates the <t>FUCCI</t> reporter that allows visualization of cells in the G1 phase. A fusion of geminin with monomeric Azami Green allows for the monitoring of cells in the G2 phase. Cells were treated with 0.03 µM 24a for the indicated duration and PI was added 1 h prior to imaging. As shown circled, only cells arrested in the G2 phase also stained for PI. Magnification, ×20. (C) Assessment of compound binding by isothermal titration calorimetry. Random, fragmented DNA was titrated into a sample of buffer, 60 µM EtBr or 100 µM 24a. Raw heat values without further deconvolution are demonstrated. PI, propidium iodide; EtBr, ethidium bromide; FUCCI, <t>fluorescence</t> ubiquitination-based cell cycle indicator.
    Fluorescence Ubiquitination Based Cell Cycle Indicator Fucci Vsv G, supplied by ATCC, 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/product/fluorescence+ubiquitination+based+cell+cycle+indicator+fucci+vsv+g/Vesicular+stomatitis+virus/pmc08923654-72-6-24
    Average 94 stars, based on 1 article reviews
    fluorescence ubiquitination based cell cycle indicator fucci vsv g - by Bioz Stars, 2026-09
    94/100 stars
    		  Buy from Supplier

    Image Search Results


    Detroit 562 cells arrested in the G2 phase are susceptible to cell death. (A) Examination of the cell cycle in response to 24a treatment. Cell cycle distribution was determined by flow cytometric analysis of PI-stained cells following 24-h treatment at the indicated doses. GM04390 is normal human fibroblasts. Values represent the mean of n=2. (B) Examination of real-time cell cycle progression using FastFUCCI-expressing Detroit 562 cells. A fusion protein of Cdt1 and monomeric Kusabira Orange 2 creates the FUCCI reporter that allows visualization of cells in the G1 phase. A fusion of geminin with monomeric Azami Green allows for the monitoring of cells in the G2 phase. Cells were treated with 0.03 µM 24a for the indicated duration and PI was added 1 h prior to imaging. As shown circled, only cells arrested in the G2 phase also stained for PI. Magnification, ×20. (C) Assessment of compound binding by isothermal titration calorimetry. Random, fragmented DNA was titrated into a sample of buffer, 60 µM EtBr or 100 µM 24a. Raw heat values without further deconvolution are demonstrated. PI, propidium iodide; EtBr, ethidium bromide; FUCCI, fluorescence ubiquitination-based cell cycle indicator.

    Journal: International Journal of Oncology

    Article Title: Discovery of a potent cytotoxic agent that promotes G 2 /M phase cell cycle arrest and apoptosis in a malignant human pharyngeal squamous carcinoma cell line

    doi: 10.3892/ijo.2022.5331

    Figure Lengend Snippet: Detroit 562 cells arrested in the G2 phase are susceptible to cell death. (A) Examination of the cell cycle in response to 24a treatment. Cell cycle distribution was determined by flow cytometric analysis of PI-stained cells following 24-h treatment at the indicated doses. GM04390 is normal human fibroblasts. Values represent the mean of n=2. (B) Examination of real-time cell cycle progression using FastFUCCI-expressing Detroit 562 cells. A fusion protein of Cdt1 and monomeric Kusabira Orange 2 creates the FUCCI reporter that allows visualization of cells in the G1 phase. A fusion of geminin with monomeric Azami Green allows for the monitoring of cells in the G2 phase. Cells were treated with 0.03 µM 24a for the indicated duration and PI was added 1 h prior to imaging. As shown circled, only cells arrested in the G2 phase also stained for PI. Magnification, ×20. (C) Assessment of compound binding by isothermal titration calorimetry. Random, fragmented DNA was titrated into a sample of buffer, 60 µM EtBr or 100 µM 24a. Raw heat values without further deconvolution are demonstrated. PI, propidium iodide; EtBr, ethidium bromide; FUCCI, fluorescence ubiquitination-based cell cycle indicator.

    Article Snippet: Construction of Detroit 562 cells expressing fluorescence ubiquitination-based cell cycle indicator (FUCCI) VSV-G pseudotyped lentiviral particles were generated from the transfection of 293T cells (ATCC) by the Lipofectamine ® 3000 reagent (Invitrogen; Thermo Fisher Scientific, Inc.) according to the manufacturer's recommendation with the 3rd generation pBOB-EF1-FastFUCCI-Puro transfer vector (plasmid no. 86849), the 2nd generation packaging plasmid pCMV-dR8.2 dpr (plasmid no. 8455) and the 2nd generation envelope plasmid pCMV-VSV-G (plasmid no. 8454) obtained from Addgene, Inc. 293T cells (at ~95% confluence in a 10-cm dish) were transfected with 10 μ g transfer vector, 5 μ g packaging plasmid and 5 μ g envelope plasmid and the media harvested 48 and 72 h post-transfection.

    Techniques: Staining, Expressing, Imaging, Binding Assay, Isothermal Titration Calorimetry, Fluorescence, Ubiquitin Proteomics