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quantum tm simply cellular microspheres  (Bangs Laboratories)

 
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    Bangs Laboratories quantum tm simply cellular microspheres
    Quantum Tm Simply Cellular Microspheres, supplied by Bangs Laboratories, 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/quantum tm simply cellular microspheres/product/Bangs Laboratories
    Average 90 stars, based on 1 article reviews
    quantum tm simply cellular microspheres - by Bioz Stars, 2026-04
    90/100 stars

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    ( A ) The binding of AF488-labeled DS-1103a to human monocyte-derived <t>macrophages</t> was analyzed by flow cytometry. The number of antibodies bound per cell was estimated using the calibration beads and is shown as geomean and geoSD (n = 3). ( B ) Far Red-labeled macrophages were co-cultured with Violet-labeled LK-2 cells and ADCP activity [%] was measured by flow cytometry. The data represent the mean ± standard error (n = 4). P-values were determined by the paired-sample t-test. ***, **, and ns indicate P < 0.001, P < 0.01, and not significant, respectively. Representative data from two independent experiments are shown.
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    ( A ) The binding of AF488-labeled DS-1103a to human monocyte-derived <t>macrophages</t> was analyzed by flow cytometry. The number of antibodies bound per cell was estimated using the calibration beads and is shown as geomean and geoSD (n = 3). ( B ) Far Red-labeled macrophages were co-cultured with Violet-labeled LK-2 cells and ADCP activity [%] was measured by flow cytometry. The data represent the mean ± standard error (n = 4). P-values were determined by the paired-sample t-test. ***, **, and ns indicate P < 0.001, P < 0.01, and not significant, respectively. Representative data from two independent experiments are shown.
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    ( A ) The binding of AF488-labeled DS-1103a to human monocyte-derived <t>macrophages</t> was analyzed by flow cytometry. The number of antibodies bound per cell was estimated using the calibration beads and is shown as geomean and geoSD (n = 3). ( B ) Far Red-labeled macrophages were co-cultured with Violet-labeled LK-2 cells and ADCP activity [%] was measured by flow cytometry. The data represent the mean ± standard error (n = 4). P-values were determined by the paired-sample t-test. ***, **, and ns indicate P < 0.001, P < 0.01, and not significant, respectively. Representative data from two independent experiments are shown.
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    quantum simply cellular microspheres  (Bangs Laboratories)
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    ( A ) The binding of AF488-labeled DS-1103a to human monocyte-derived <t>macrophages</t> was analyzed by flow cytometry. The number of antibodies bound per cell was estimated using the calibration beads and is shown as geomean and geoSD (n = 3). ( B ) Far Red-labeled macrophages were co-cultured with Violet-labeled LK-2 cells and ADCP activity [%] was measured by flow cytometry. The data represent the mean ± standard error (n = 4). P-values were determined by the paired-sample t-test. ***, **, and ns indicate P < 0.001, P < 0.01, and not significant, respectively. Representative data from two independent experiments are shown.
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    ( A ) The binding of AF488-labeled DS-1103a to human monocyte-derived <t>macrophages</t> was analyzed by flow cytometry. The number of antibodies bound per cell was estimated using the calibration beads and is shown as geomean and geoSD (n = 3). ( B ) Far Red-labeled macrophages were co-cultured with Violet-labeled LK-2 cells and ADCP activity [%] was measured by flow cytometry. The data represent the mean ± standard error (n = 4). P-values were determined by the paired-sample t-test. ***, **, and ns indicate P < 0.001, P < 0.01, and not significant, respectively. Representative data from two independent experiments are shown.
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    ( A ) The binding of AF488-labeled DS-1103a to human monocyte-derived <t>macrophages</t> was analyzed by flow cytometry. The number of antibodies bound per cell was estimated using the calibration beads and is shown as geomean and geoSD (n = 3). ( B ) Far Red-labeled macrophages were co-cultured with Violet-labeled LK-2 cells and ADCP activity [%] was measured by flow cytometry. The data represent the mean ± standard error (n = 4). P-values were determined by the paired-sample t-test. ***, **, and ns indicate P < 0.001, P < 0.01, and not significant, respectively. Representative data from two independent experiments are shown.
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    calibrated microspheres quantum simply cellular  (Bangs Laboratories)
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    ( A ) The binding of AF488-labeled DS-1103a to human monocyte-derived <t>macrophages</t> was analyzed by flow cytometry. The number of antibodies bound per cell was estimated using the calibration beads and is shown as geomean and geoSD (n = 3). ( B ) Far Red-labeled macrophages were co-cultured with Violet-labeled LK-2 cells and ADCP activity [%] was measured by flow cytometry. The data represent the mean ± standard error (n = 4). P-values were determined by the paired-sample t-test. ***, **, and ns indicate P < 0.001, P < 0.01, and not significant, respectively. Representative data from two independent experiments are shown.
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    ( A ) The binding of AF488-labeled DS-1103a to human monocyte-derived macrophages was analyzed by flow cytometry. The number of antibodies bound per cell was estimated using the calibration beads and is shown as geomean and geoSD (n = 3). ( B ) Far Red-labeled macrophages were co-cultured with Violet-labeled LK-2 cells and ADCP activity [%] was measured by flow cytometry. The data represent the mean ± standard error (n = 4). P-values were determined by the paired-sample t-test. ***, **, and ns indicate P < 0.001, P < 0.01, and not significant, respectively. Representative data from two independent experiments are shown.

    Journal: PLOS ONE

    Article Title: Blockade of SIRPα-CD47 axis by anti-SIRPα antibody enhances anti-tumor activity of DXd antibody-drug conjugates

    doi: 10.1371/journal.pone.0304985

    Figure Lengend Snippet: ( A ) The binding of AF488-labeled DS-1103a to human monocyte-derived macrophages was analyzed by flow cytometry. The number of antibodies bound per cell was estimated using the calibration beads and is shown as geomean and geoSD (n = 3). ( B ) Far Red-labeled macrophages were co-cultured with Violet-labeled LK-2 cells and ADCP activity [%] was measured by flow cytometry. The data represent the mean ± standard error (n = 4). P-values were determined by the paired-sample t-test. ***, **, and ns indicate P < 0.001, P < 0.01, and not significant, respectively. Representative data from two independent experiments are shown.

    Article Snippet: To quantify DS-1103a binding to macrophages, anti-IgG, Human, Goat-Poly, Microsphere, Quantum Simply Cellular (Bangs Laboratories, Technology Drive Fishers, IN) was used.

    Techniques: Binding Assay, Labeling, Derivative Assay, Flow Cytometry, Cell Culture, Activity Assay