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cd19 apc ebioscience ilt2 pe  (Thermo Fisher)


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    Structured Review

    Thermo Fisher cd19 apc ebioscience ilt2 pe
    Patient and tumor characteristics
    Cd19 Apc Ebioscience Ilt2 Pe, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cd19+apc+ebioscience+ilt2+pe/pmc06145700-140-17-18?v=Thermo+Fisher
    Average 86 stars, based on 1 article reviews
    cd19 apc ebioscience ilt2 pe - by Bioz Stars, 2026-08
    86/100 stars

    Images

    1) Product Images from "Prediction of non-muscle-invasive bladder cancer recurrence by measurement of checkpoint HLAG’s receptor ILT2 on peripheral CD8 + T cells"

    Article Title: Prediction of non-muscle-invasive bladder cancer recurrence by measurement of checkpoint HLAG’s receptor ILT2 on peripheral CD8 + T cells

    Journal: Oncotarget

    doi: 10.18632/oncotarget.26036

    Patient and tumor characteristics
    Figure Legend Snippet: Patient and tumor characteristics

    Techniques Used:

    ( A ) HLA-G expression in NMIBC biopsies. Two representative results obtained are shown. Brown labelling indicates HLA-G positivity. ( B ) Representative images of the results obtained for ILT2 cell-surface expression on CD8 + T cells from NMIBC patients with low (left) and high (right). Proportion of the ILT2-positive population within the CD8 + T cell population is indicated. ( C ) ILT2 expression levels on peripheral CD3 + CD4 + T cells and CD3 + CD8 + T cells for 25 healthy donors (HD), 20 aged-matched controls (Aged-matched), and 27 (for CD4 + T cells) or 76 (for CD8 + T cells) NMIBC patients. ( D ) Proportion of ILT2 + peripheral CD3 + CD4 + T cells and CD3 + CD8 + T cells at the time of inclusion from NMIBC patients who recurred and did not recur within 12 months. ( E ) Proportion of ILT2 + peripheral CD3 + CD8 + T cells at the time of inclusion from NMIBC patients who recurred and did not recur within 24 months. Mean and standard deviation are shown. P was calculated using Mann–Whitney test.
    Figure Legend Snippet: ( A ) HLA-G expression in NMIBC biopsies. Two representative results obtained are shown. Brown labelling indicates HLA-G positivity. ( B ) Representative images of the results obtained for ILT2 cell-surface expression on CD8 + T cells from NMIBC patients with low (left) and high (right). Proportion of the ILT2-positive population within the CD8 + T cell population is indicated. ( C ) ILT2 expression levels on peripheral CD3 + CD4 + T cells and CD3 + CD8 + T cells for 25 healthy donors (HD), 20 aged-matched controls (Aged-matched), and 27 (for CD4 + T cells) or 76 (for CD8 + T cells) NMIBC patients. ( D ) Proportion of ILT2 + peripheral CD3 + CD4 + T cells and CD3 + CD8 + T cells at the time of inclusion from NMIBC patients who recurred and did not recur within 12 months. ( E ) Proportion of ILT2 + peripheral CD3 + CD8 + T cells at the time of inclusion from NMIBC patients who recurred and did not recur within 24 months. Mean and standard deviation are shown. P was calculated using Mann–Whitney test.

    Techniques Used: Expressing, Standard Deviation, MANN-WHITNEY

    ( A ) Analysis for the whole cohort. ( B ) Analysis for incident patients. ( C ) Analysis for prevalent patients. Recurrence-free survival curves are shown for Low (≤18% CD8 + ILT2 + T cells among CD8 + T cells) vs intermediate (19%–45% CD8 + ILT2 + T cells among CD8 + T cells) vs high (≥46% CD8 + ILT2 + T cells among CD8 + T cells).
    Figure Legend Snippet: ( A ) Analysis for the whole cohort. ( B ) Analysis for incident patients. ( C ) Analysis for prevalent patients. Recurrence-free survival curves are shown for Low (≤18% CD8 + ILT2 + T cells among CD8 + T cells) vs intermediate (19%–45% CD8 + ILT2 + T cells among CD8 + T cells) vs high (≥46% CD8 + ILT2 + T cells among CD8 + T cells).

    Techniques Used:

    Cox regression for factors associated with tumor recurrence
    Figure Legend Snippet: Cox regression for factors associated with tumor recurrence

    Techniques Used: Isolation

    Calculation of the concordance index at different time points of the model with clinical variables alone, with  CD8-ILT2  alone and with both clinical variables and  CD8-ILT2
    Figure Legend Snippet: Calculation of the concordance index at different time points of the model with clinical variables alone, with CD8-ILT2 alone and with both clinical variables and CD8-ILT2

    Techniques Used:



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    86
    Thermo Fisher cd19 apc ebioscience ilt2 pe
    Patient and tumor characteristics
    Cd19 Apc Ebioscience Ilt2 Pe, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cd19+apc+ebioscience+ilt2+pe/pmc06145700-140-17-18?v=Thermo+Fisher
    Average 86 stars, based on 1 article reviews
    cd19 apc ebioscience ilt2 pe - by Bioz Stars, 2026-08
    86/100 stars
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    Patient and tumor characteristics

    Journal: Oncotarget

    Article Title: Prediction of non-muscle-invasive bladder cancer recurrence by measurement of checkpoint HLAG’s receptor ILT2 on peripheral CD8 + T cells

    doi: 10.18632/oncotarget.26036

    Figure Lengend Snippet: Patient and tumor characteristics

    Article Snippet: The following antibodies were used for cell surface staining and phenotyping: from Miltenyi Biotec: CD3-PerCP, CD4-VioBright-FITC, CD8-APC-Vio770, CD19-APC eBioscience: ILT2-PE (Clone HP-F1).

    Techniques:

    ( A ) HLA-G expression in NMIBC biopsies. Two representative results obtained are shown. Brown labelling indicates HLA-G positivity. ( B ) Representative images of the results obtained for ILT2 cell-surface expression on CD8 + T cells from NMIBC patients with low (left) and high (right). Proportion of the ILT2-positive population within the CD8 + T cell population is indicated. ( C ) ILT2 expression levels on peripheral CD3 + CD4 + T cells and CD3 + CD8 + T cells for 25 healthy donors (HD), 20 aged-matched controls (Aged-matched), and 27 (for CD4 + T cells) or 76 (for CD8 + T cells) NMIBC patients. ( D ) Proportion of ILT2 + peripheral CD3 + CD4 + T cells and CD3 + CD8 + T cells at the time of inclusion from NMIBC patients who recurred and did not recur within 12 months. ( E ) Proportion of ILT2 + peripheral CD3 + CD8 + T cells at the time of inclusion from NMIBC patients who recurred and did not recur within 24 months. Mean and standard deviation are shown. P was calculated using Mann–Whitney test.

    Journal: Oncotarget

    Article Title: Prediction of non-muscle-invasive bladder cancer recurrence by measurement of checkpoint HLAG’s receptor ILT2 on peripheral CD8 + T cells

    doi: 10.18632/oncotarget.26036

    Figure Lengend Snippet: ( A ) HLA-G expression in NMIBC biopsies. Two representative results obtained are shown. Brown labelling indicates HLA-G positivity. ( B ) Representative images of the results obtained for ILT2 cell-surface expression on CD8 + T cells from NMIBC patients with low (left) and high (right). Proportion of the ILT2-positive population within the CD8 + T cell population is indicated. ( C ) ILT2 expression levels on peripheral CD3 + CD4 + T cells and CD3 + CD8 + T cells for 25 healthy donors (HD), 20 aged-matched controls (Aged-matched), and 27 (for CD4 + T cells) or 76 (for CD8 + T cells) NMIBC patients. ( D ) Proportion of ILT2 + peripheral CD3 + CD4 + T cells and CD3 + CD8 + T cells at the time of inclusion from NMIBC patients who recurred and did not recur within 12 months. ( E ) Proportion of ILT2 + peripheral CD3 + CD8 + T cells at the time of inclusion from NMIBC patients who recurred and did not recur within 24 months. Mean and standard deviation are shown. P was calculated using Mann–Whitney test.

    Article Snippet: The following antibodies were used for cell surface staining and phenotyping: from Miltenyi Biotec: CD3-PerCP, CD4-VioBright-FITC, CD8-APC-Vio770, CD19-APC eBioscience: ILT2-PE (Clone HP-F1).

    Techniques: Expressing, Standard Deviation, MANN-WHITNEY

    ( A ) Analysis for the whole cohort. ( B ) Analysis for incident patients. ( C ) Analysis for prevalent patients. Recurrence-free survival curves are shown for Low (≤18% CD8 + ILT2 + T cells among CD8 + T cells) vs intermediate (19%–45% CD8 + ILT2 + T cells among CD8 + T cells) vs high (≥46% CD8 + ILT2 + T cells among CD8 + T cells).

    Journal: Oncotarget

    Article Title: Prediction of non-muscle-invasive bladder cancer recurrence by measurement of checkpoint HLAG’s receptor ILT2 on peripheral CD8 + T cells

    doi: 10.18632/oncotarget.26036

    Figure Lengend Snippet: ( A ) Analysis for the whole cohort. ( B ) Analysis for incident patients. ( C ) Analysis for prevalent patients. Recurrence-free survival curves are shown for Low (≤18% CD8 + ILT2 + T cells among CD8 + T cells) vs intermediate (19%–45% CD8 + ILT2 + T cells among CD8 + T cells) vs high (≥46% CD8 + ILT2 + T cells among CD8 + T cells).

    Article Snippet: The following antibodies were used for cell surface staining and phenotyping: from Miltenyi Biotec: CD3-PerCP, CD4-VioBright-FITC, CD8-APC-Vio770, CD19-APC eBioscience: ILT2-PE (Clone HP-F1).

    Techniques:

    Cox regression for factors associated with tumor recurrence

    Journal: Oncotarget

    Article Title: Prediction of non-muscle-invasive bladder cancer recurrence by measurement of checkpoint HLAG’s receptor ILT2 on peripheral CD8 + T cells

    doi: 10.18632/oncotarget.26036

    Figure Lengend Snippet: Cox regression for factors associated with tumor recurrence

    Article Snippet: The following antibodies were used for cell surface staining and phenotyping: from Miltenyi Biotec: CD3-PerCP, CD4-VioBright-FITC, CD8-APC-Vio770, CD19-APC eBioscience: ILT2-PE (Clone HP-F1).

    Techniques: Isolation

    Calculation of the concordance index at different time points of the model with clinical variables alone, with  CD8-ILT2  alone and with both clinical variables and  CD8-ILT2

    Journal: Oncotarget

    Article Title: Prediction of non-muscle-invasive bladder cancer recurrence by measurement of checkpoint HLAG’s receptor ILT2 on peripheral CD8 + T cells

    doi: 10.18632/oncotarget.26036

    Figure Lengend Snippet: Calculation of the concordance index at different time points of the model with clinical variables alone, with CD8-ILT2 alone and with both clinical variables and CD8-ILT2

    Article Snippet: The following antibodies were used for cell surface staining and phenotyping: from Miltenyi Biotec: CD3-PerCP, CD4-VioBright-FITC, CD8-APC-Vio770, CD19-APC eBioscience: ILT2-PE (Clone HP-F1).

    Techniques: