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cellular proliferation rate  (Dojindo Labs)


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    Dojindo Labs cellular proliferation rate
    Scatter plot showing the correlation between flow cytometry median fluorescence intensity of ICG; 635 780/60 (y-axis) and cell line <t>proliferation</t> rate; CCK-8 (x-axis). Labelled data points indicate each cancer cell line, Mean ± SEM, with linear trend line (dotted blue). Correlation was calculated using SPSS software (V.27) non-parametric Spearman’s rho function; Rs = 1.000, p<0.001 (2-tailed). The analysed MFI and CCK data were taken as the mean value over three experiments, repeated on separate occasions. MFI= median fluorescence intensity, CCK-8= cell counting kit-8, SEM= standard error of the mean , ICG= indocyanine green.
    Cellular Proliferation Rate, supplied by Dojindo Labs, used in various techniques. Bioz Stars score: 99/100, based on 57434 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/cellular proliferation rate/product/Dojindo Labs
    Average 99 stars, based on 57434 article reviews
    cellular proliferation rate - by Bioz Stars, 2026-06
    99/100 stars

    Images

    1) Product Images from "Investigating the mechanisms of indocyanine green (ICG) cellular uptake in sarcoma"

    Article Title: Investigating the mechanisms of indocyanine green (ICG) cellular uptake in sarcoma

    Journal: bioRxiv

    doi: 10.1101/2021.04.05.438013

    Scatter plot showing the correlation between flow cytometry median fluorescence intensity of ICG; 635 780/60 (y-axis) and cell line proliferation rate; CCK-8 (x-axis). Labelled data points indicate each cancer cell line, Mean ± SEM, with linear trend line (dotted blue). Correlation was calculated using SPSS software (V.27) non-parametric Spearman’s rho function; Rs = 1.000, p<0.001 (2-tailed). The analysed MFI and CCK data were taken as the mean value over three experiments, repeated on separate occasions. MFI= median fluorescence intensity, CCK-8= cell counting kit-8, SEM= standard error of the mean , ICG= indocyanine green.
    Figure Legend Snippet: Scatter plot showing the correlation between flow cytometry median fluorescence intensity of ICG; 635 780/60 (y-axis) and cell line proliferation rate; CCK-8 (x-axis). Labelled data points indicate each cancer cell line, Mean ± SEM, with linear trend line (dotted blue). Correlation was calculated using SPSS software (V.27) non-parametric Spearman’s rho function; Rs = 1.000, p<0.001 (2-tailed). The analysed MFI and CCK data were taken as the mean value over three experiments, repeated on separate occasions. MFI= median fluorescence intensity, CCK-8= cell counting kit-8, SEM= standard error of the mean , ICG= indocyanine green.

    Techniques Used: Flow Cytometry, Fluorescence, CCK-8 Assay, Software, Cell Counting

    Scatter plots showing the correlation between ICG retention after 24hrs and cell line proliferation rate. (a) Scatter graph showing the correlation between MFI after 0.5hrs (blue) and 0.5hrs + 24hrs (orange) incubation in 25μM ICG vs proliferation rate (CCK) across all cell lines. The MFI data points were calculated as the average from two experiments repeated on separate occasions. Spearman’s rho function; Rs = 0.9, p= 0.037 for both data sets. (b) Scatter graph comparing ICG retention percentage to proliferation rate across all cell lines; Rs = 0.3, p=0.624. Flow cytometry data available in the Supporting Information. MFI= median fluorescence intensity, CCK-8= cell counting kit-8 , ICG= indocyanine green.
    Figure Legend Snippet: Scatter plots showing the correlation between ICG retention after 24hrs and cell line proliferation rate. (a) Scatter graph showing the correlation between MFI after 0.5hrs (blue) and 0.5hrs + 24hrs (orange) incubation in 25μM ICG vs proliferation rate (CCK) across all cell lines. The MFI data points were calculated as the average from two experiments repeated on separate occasions. Spearman’s rho function; Rs = 0.9, p= 0.037 for both data sets. (b) Scatter graph comparing ICG retention percentage to proliferation rate across all cell lines; Rs = 0.3, p=0.624. Flow cytometry data available in the Supporting Information. MFI= median fluorescence intensity, CCK-8= cell counting kit-8 , ICG= indocyanine green.

    Techniques Used: Incubation, Flow Cytometry, Fluorescence, CCK-8 Assay, Cell Counting



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    Scatter plot showing the correlation between flow cytometry median fluorescence intensity of ICG; 635 780/60 (y-axis) and cell line <t>proliferation</t> rate; CCK-8 (x-axis). Labelled data points indicate each cancer cell line, Mean ± SEM, with linear trend line (dotted blue). Correlation was calculated using SPSS software (V.27) non-parametric Spearman’s rho function; Rs = 1.000, p<0.001 (2-tailed). The analysed MFI and CCK data were taken as the mean value over three experiments, repeated on separate occasions. MFI= median fluorescence intensity, CCK-8= cell counting kit-8, SEM= standard error of the mean , ICG= indocyanine green.
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    Scatter plot showing the correlation between flow cytometry median fluorescence intensity of ICG; 635 780/60 (y-axis) and cell line <t>proliferation</t> rate; CCK-8 (x-axis). Labelled data points indicate each cancer cell line, Mean ± SEM, with linear trend line (dotted blue). Correlation was calculated using SPSS software (V.27) non-parametric Spearman’s rho function; Rs = 1.000, p<0.001 (2-tailed). The analysed MFI and CCK data were taken as the mean value over three experiments, repeated on separate occasions. MFI= median fluorescence intensity, CCK-8= cell counting kit-8, SEM= standard error of the mean , ICG= indocyanine green.
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    Scatter plot showing the correlation between flow cytometry median fluorescence intensity of ICG; 635 780/60 (y-axis) and cell line <t>proliferation</t> rate; CCK-8 (x-axis). Labelled data points indicate each cancer cell line, Mean ± SEM, with linear trend line (dotted blue). Correlation was calculated using SPSS software (V.27) non-parametric Spearman’s rho function; Rs = 1.000, p<0.001 (2-tailed). The analysed MFI and CCK data were taken as the mean value over three experiments, repeated on separate occasions. MFI= median fluorescence intensity, CCK-8= cell counting kit-8, SEM= standard error of the mean , ICG= indocyanine green.
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    Image Search Results


    Scatter plot showing the correlation between flow cytometry median fluorescence intensity of ICG; 635 780/60 (y-axis) and cell line proliferation rate; CCK-8 (x-axis). Labelled data points indicate each cancer cell line, Mean ± SEM, with linear trend line (dotted blue). Correlation was calculated using SPSS software (V.27) non-parametric Spearman’s rho function; Rs = 1.000, p<0.001 (2-tailed). The analysed MFI and CCK data were taken as the mean value over three experiments, repeated on separate occasions. MFI= median fluorescence intensity, CCK-8= cell counting kit-8, SEM= standard error of the mean , ICG= indocyanine green.

    Journal: bioRxiv

    Article Title: Investigating the mechanisms of indocyanine green (ICG) cellular uptake in sarcoma

    doi: 10.1101/2021.04.05.438013

    Figure Lengend Snippet: Scatter plot showing the correlation between flow cytometry median fluorescence intensity of ICG; 635 780/60 (y-axis) and cell line proliferation rate; CCK-8 (x-axis). Labelled data points indicate each cancer cell line, Mean ± SEM, with linear trend line (dotted blue). Correlation was calculated using SPSS software (V.27) non-parametric Spearman’s rho function; Rs = 1.000, p<0.001 (2-tailed). The analysed MFI and CCK data were taken as the mean value over three experiments, repeated on separate occasions. MFI= median fluorescence intensity, CCK-8= cell counting kit-8, SEM= standard error of the mean , ICG= indocyanine green.

    Article Snippet: Cellular proliferation rate was assessed using Cell Counting Kit-8 (CCK-8, Dojindo Labatories, CK04-11) as per the manufacturer’s manual.

    Techniques: Flow Cytometry, Fluorescence, CCK-8 Assay, Software, Cell Counting

    Scatter plots showing the correlation between ICG retention after 24hrs and cell line proliferation rate. (a) Scatter graph showing the correlation between MFI after 0.5hrs (blue) and 0.5hrs + 24hrs (orange) incubation in 25μM ICG vs proliferation rate (CCK) across all cell lines. The MFI data points were calculated as the average from two experiments repeated on separate occasions. Spearman’s rho function; Rs = 0.9, p= 0.037 for both data sets. (b) Scatter graph comparing ICG retention percentage to proliferation rate across all cell lines; Rs = 0.3, p=0.624. Flow cytometry data available in the Supporting Information. MFI= median fluorescence intensity, CCK-8= cell counting kit-8 , ICG= indocyanine green.

    Journal: bioRxiv

    Article Title: Investigating the mechanisms of indocyanine green (ICG) cellular uptake in sarcoma

    doi: 10.1101/2021.04.05.438013

    Figure Lengend Snippet: Scatter plots showing the correlation between ICG retention after 24hrs and cell line proliferation rate. (a) Scatter graph showing the correlation between MFI after 0.5hrs (blue) and 0.5hrs + 24hrs (orange) incubation in 25μM ICG vs proliferation rate (CCK) across all cell lines. The MFI data points were calculated as the average from two experiments repeated on separate occasions. Spearman’s rho function; Rs = 0.9, p= 0.037 for both data sets. (b) Scatter graph comparing ICG retention percentage to proliferation rate across all cell lines; Rs = 0.3, p=0.624. Flow cytometry data available in the Supporting Information. MFI= median fluorescence intensity, CCK-8= cell counting kit-8 , ICG= indocyanine green.

    Article Snippet: Cellular proliferation rate was assessed using Cell Counting Kit-8 (CCK-8, Dojindo Labatories, CK04-11) as per the manufacturer’s manual.

    Techniques: Incubation, Flow Cytometry, Fluorescence, CCK-8 Assay, Cell Counting