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cd3 receptor  (Miltenyi Biotec)


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    Structured Review

    Miltenyi Biotec cd3 receptor
    Cd3 Receptor, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 98/100, based on 30 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/cd3 receptor/product/Miltenyi Biotec
    Average 98 stars, based on 30 article reviews
    cd3 receptor - by Bioz Stars, 2026-05
    98/100 stars

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    ( A ) RO NOD mice with blood glucose levels above 11.1 mmol/L were treated with anti–mouse <t>CD3</t> antibody (2.5 μg/day) for 5 consecutive days. Blood glucose concentrations were monitored 3 times per week for 28 days following treatment initiation. At day 28, mice were classified as Rs or NRs on the basis of glycemic control. Pancreas and peripheral blood samples were collected at this time point for further analysis. ( B ) Kaplan-Meier survival curve shows the percentage of remission from disease of RO NOD mice after anti–mouse CD3 therapy. Black and white symbols indicate treated and untreated samples, respectively. ( C ) Individual glycemia levels of untreated mice, anti–mouse CD3 R mice, and anti–mouse CD3 NR mice during the study follow-up are shown in yellow, blue, and red, respectively. Normoglycemia threshold (11.1 mmol/L) is depicted by the red line. In B, the Mantel-Cox log-rank test was used for statistical comparison between groups.
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    a Schematic illustration of the treatment and analysis schedule for mice bearing orthotopic LLC tumors. b – f Representative flow cytometric analysis profiles and relative quantifications of CD8 + T cells (CD45 + <t>CD3</t> + CD8 + ) ( b ), Treg cells (CD45 + CD4 + FOXP3 + ) ( c ), MDSCs (CD45 + CD11b + Gr-1 + ) ( d ), IFN-γ-secreting CD8 + T cells (CD45 + CD3 + CD8 + IFN-γ + ) ( e ), and CD8 + T cell proliferation (CD45 + CD3 + CD8 + Ki67 + ) ( f ) within the TME following the indicated treatments. g – i Quantification of the infiltration of CD45 + immune cells ( g ), CD4 + T cells ( h ), and CD8 + T cells ( i ) into lung tumors using flow cytometry. j – n ELISA analysis of IFN-γ ( j ), IL-2 ( k ), IL-12p70 ( l ), TNF-α ( m ), and IL-10 ( n ) levels in lung tumors of mice following the indicated treatments. Flow cytometry gating strategies are shown in Supplementary Fig. . All data are from n = 5 mice and are presented as mean ± s.d. Statistical analysis was performed using one-way ANOVA with Bonferroni’s multiple comparisons test. P values as indicated. Source data are provided as a Source Data file.
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    ( A ) RO NOD mice with blood glucose levels above 11.1 mmol/L were treated with anti–mouse CD3 antibody (2.5 μg/day) for 5 consecutive days. Blood glucose concentrations were monitored 3 times per week for 28 days following treatment initiation. At day 28, mice were classified as Rs or NRs on the basis of glycemic control. Pancreas and peripheral blood samples were collected at this time point for further analysis. ( B ) Kaplan-Meier survival curve shows the percentage of remission from disease of RO NOD mice after anti–mouse CD3 therapy. Black and white symbols indicate treated and untreated samples, respectively. ( C ) Individual glycemia levels of untreated mice, anti–mouse CD3 R mice, and anti–mouse CD3 NR mice during the study follow-up are shown in yellow, blue, and red, respectively. Normoglycemia threshold (11.1 mmol/L) is depicted by the red line. In B, the Mantel-Cox log-rank test was used for statistical comparison between groups.

    Journal: The Journal of Clinical Investigation

    Article Title: Neutrophil-enriched gene signature correlates with teplizumab therapy resistance in different stages of type 1 diabetes

    doi: 10.1172/JCI176403

    Figure Lengend Snippet: ( A ) RO NOD mice with blood glucose levels above 11.1 mmol/L were treated with anti–mouse CD3 antibody (2.5 μg/day) for 5 consecutive days. Blood glucose concentrations were monitored 3 times per week for 28 days following treatment initiation. At day 28, mice were classified as Rs or NRs on the basis of glycemic control. Pancreas and peripheral blood samples were collected at this time point for further analysis. ( B ) Kaplan-Meier survival curve shows the percentage of remission from disease of RO NOD mice after anti–mouse CD3 therapy. Black and white symbols indicate treated and untreated samples, respectively. ( C ) Individual glycemia levels of untreated mice, anti–mouse CD3 R mice, and anti–mouse CD3 NR mice during the study follow-up are shown in yellow, blue, and red, respectively. Normoglycemia threshold (11.1 mmol/L) is depicted by the red line. In B, the Mantel-Cox log-rank test was used for statistical comparison between groups.

    Article Snippet: RO NOD mice were bled via the submandibular vein and treated for 5 consecutive days with 2.5 μg/d hamster anti–mouse CD3 mAb (clone 145-2C11, BioXCell) and monitored for a period of 28 days (CITE-Seq and follow-up) ( ).

    Techniques: Control, Comparison

    a Schematic illustration of the treatment and analysis schedule for mice bearing orthotopic LLC tumors. b – f Representative flow cytometric analysis profiles and relative quantifications of CD8 + T cells (CD45 + CD3 + CD8 + ) ( b ), Treg cells (CD45 + CD4 + FOXP3 + ) ( c ), MDSCs (CD45 + CD11b + Gr-1 + ) ( d ), IFN-γ-secreting CD8 + T cells (CD45 + CD3 + CD8 + IFN-γ + ) ( e ), and CD8 + T cell proliferation (CD45 + CD3 + CD8 + Ki67 + ) ( f ) within the TME following the indicated treatments. g – i Quantification of the infiltration of CD45 + immune cells ( g ), CD4 + T cells ( h ), and CD8 + T cells ( i ) into lung tumors using flow cytometry. j – n ELISA analysis of IFN-γ ( j ), IL-2 ( k ), IL-12p70 ( l ), TNF-α ( m ), and IL-10 ( n ) levels in lung tumors of mice following the indicated treatments. Flow cytometry gating strategies are shown in Supplementary Fig. . All data are from n = 5 mice and are presented as mean ± s.d. Statistical analysis was performed using one-way ANOVA with Bonferroni’s multiple comparisons test. P values as indicated. Source data are provided as a Source Data file.

    Journal: Nature Communications

    Article Title: Modulating tumor collagen fiber alignment for enhanced lung cancer immunotherapy via inhaled RNA

    doi: 10.1038/s41467-025-63415-0

    Figure Lengend Snippet: a Schematic illustration of the treatment and analysis schedule for mice bearing orthotopic LLC tumors. b – f Representative flow cytometric analysis profiles and relative quantifications of CD8 + T cells (CD45 + CD3 + CD8 + ) ( b ), Treg cells (CD45 + CD4 + FOXP3 + ) ( c ), MDSCs (CD45 + CD11b + Gr-1 + ) ( d ), IFN-γ-secreting CD8 + T cells (CD45 + CD3 + CD8 + IFN-γ + ) ( e ), and CD8 + T cell proliferation (CD45 + CD3 + CD8 + Ki67 + ) ( f ) within the TME following the indicated treatments. g – i Quantification of the infiltration of CD45 + immune cells ( g ), CD4 + T cells ( h ), and CD8 + T cells ( i ) into lung tumors using flow cytometry. j – n ELISA analysis of IFN-γ ( j ), IL-2 ( k ), IL-12p70 ( l ), TNF-α ( m ), and IL-10 ( n ) levels in lung tumors of mice following the indicated treatments. Flow cytometry gating strategies are shown in Supplementary Fig. . All data are from n = 5 mice and are presented as mean ± s.d. Statistical analysis was performed using one-way ANOVA with Bonferroni’s multiple comparisons test. P values as indicated. Source data are provided as a Source Data file.

    Article Snippet: The isolated CD8 T cells were resuspended in RPMI 1640 supplemented with 10% FBS, 1% penicillin/streptomycin, and 0.1% 2-mercaptoethanol (Thermo Fisher Scientific) and then cultured in a 48-well plate pretreated with anti-mouse CD3 and CD28 antibodies (Bio X Cell).

    Techniques: Flow Cytometry, Enzyme-linked Immunosorbent Assay