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biotinylated anti tcrβ  (Novus Biologicals)


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    Novus Biologicals biotinylated anti tcrβ
    Figure 4. Expression of Cdc42-Q61L selectively impairs internalization of the TCR-CD3 complex. (A) Schematic of the flow-cytometry based internalization assay; cells are labelled at 4 ◦C with a functional <t>biotinylated</t> anti-CD3ε and either (yellow) directly stained with Pacific Blue-streptavidin to measure surface expression of TCR-CD3 complex in resting cells, (blue) activated by incubation at 37 ◦C and stained with Pacific Blue-streptavidin to detect remaining TCR-CD3 at the cell surface after activation-induced internalization, or (red) activated by incubation at 37 ◦C, re-labelled with biotinylated anti-CD3ε and stained with Pacific Blue-streptavidin to detect total surface TCR-CD3 in activated cells. (B) Remaining TCR-CD3 at the cell surface detected by an antibody against CD3ε (clone OKT3) after activation-induced internalization in cells expressing an empty vector, GFP-WT-Cdc42, GFP-Cdc42-Q61L, or GFP-Cdc42-T17N. (C) Surface expression of TCR-CD3 complex in cells expressing the same constructs as in (B). (D) Total surface TCR-CD3 in activated cells transfected as in (B). (E) Internalization of biotinylated Tf detected with Pacific Blue-streptavidin after incubation at 37 ◦C as described for anti-CD3ε in (A), in cells activated by soluble anti-CD3ε and expressing the same constructs as in (B). (F) Surface expression of Tf in cells expressing the same constructs as in (B). (G) Total Tf at the cell surface detected with biotinylated Tf and Pacific Blue-streptavidin in activated cells as in (F). Each data point represents the mean of an individual experiment. Small horizontal lines indicate mean (±SEM), ** p < 0.01, n.s. not significant, unpaired, two-tailed student’s t-test.
    Biotinylated Anti Tcrβ, supplied by Novus Biologicals, 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/product/biotinylated+anti+tcr%CE%B2/TRBC1+Antibody+(JOVI%2E1)+%5BBiotin%5D/pm31690048-60-18-22
    Average 90 stars, based on 1 article reviews
    biotinylated anti tcrβ - by Bioz Stars, 2026-09
    90/100 stars

    Images

    1) Product Images from "Cdc42 Couples T Cell Receptor Endocytosis to GRAF1-Mediated Tubular Invaginations of the Plasma Membrane."

    Article Title: Cdc42 Couples T Cell Receptor Endocytosis to GRAF1-Mediated Tubular Invaginations of the Plasma Membrane.

    Journal: Cells

    doi: 10.3390/cells8111388

    Figure 4. Expression of Cdc42-Q61L selectively impairs internalization of the TCR-CD3 complex. (A) Schematic of the flow-cytometry based internalization assay; cells are labelled at 4 ◦C with a functional biotinylated anti-CD3ε and either (yellow) directly stained with Pacific Blue-streptavidin to measure surface expression of TCR-CD3 complex in resting cells, (blue) activated by incubation at 37 ◦C and stained with Pacific Blue-streptavidin to detect remaining TCR-CD3 at the cell surface after activation-induced internalization, or (red) activated by incubation at 37 ◦C, re-labelled with biotinylated anti-CD3ε and stained with Pacific Blue-streptavidin to detect total surface TCR-CD3 in activated cells. (B) Remaining TCR-CD3 at the cell surface detected by an antibody against CD3ε (clone OKT3) after activation-induced internalization in cells expressing an empty vector, GFP-WT-Cdc42, GFP-Cdc42-Q61L, or GFP-Cdc42-T17N. (C) Surface expression of TCR-CD3 complex in cells expressing the same constructs as in (B). (D) Total surface TCR-CD3 in activated cells transfected as in (B). (E) Internalization of biotinylated Tf detected with Pacific Blue-streptavidin after incubation at 37 ◦C as described for anti-CD3ε in (A), in cells activated by soluble anti-CD3ε and expressing the same constructs as in (B). (F) Surface expression of Tf in cells expressing the same constructs as in (B). (G) Total Tf at the cell surface detected with biotinylated Tf and Pacific Blue-streptavidin in activated cells as in (F). Each data point represents the mean of an individual experiment. Small horizontal lines indicate mean (±SEM), ** p < 0.01, n.s. not significant, unpaired, two-tailed student’s t-test.
    Figure Legend Snippet: Figure 4. Expression of Cdc42-Q61L selectively impairs internalization of the TCR-CD3 complex. (A) Schematic of the flow-cytometry based internalization assay; cells are labelled at 4 ◦C with a functional biotinylated anti-CD3ε and either (yellow) directly stained with Pacific Blue-streptavidin to measure surface expression of TCR-CD3 complex in resting cells, (blue) activated by incubation at 37 ◦C and stained with Pacific Blue-streptavidin to detect remaining TCR-CD3 at the cell surface after activation-induced internalization, or (red) activated by incubation at 37 ◦C, re-labelled with biotinylated anti-CD3ε and stained with Pacific Blue-streptavidin to detect total surface TCR-CD3 in activated cells. (B) Remaining TCR-CD3 at the cell surface detected by an antibody against CD3ε (clone OKT3) after activation-induced internalization in cells expressing an empty vector, GFP-WT-Cdc42, GFP-Cdc42-Q61L, or GFP-Cdc42-T17N. (C) Surface expression of TCR-CD3 complex in cells expressing the same constructs as in (B). (D) Total surface TCR-CD3 in activated cells transfected as in (B). (E) Internalization of biotinylated Tf detected with Pacific Blue-streptavidin after incubation at 37 ◦C as described for anti-CD3ε in (A), in cells activated by soluble anti-CD3ε and expressing the same constructs as in (B). (F) Surface expression of Tf in cells expressing the same constructs as in (B). (G) Total Tf at the cell surface detected with biotinylated Tf and Pacific Blue-streptavidin in activated cells as in (F). Each data point represents the mean of an individual experiment. Small horizontal lines indicate mean (±SEM), ** p < 0.01, n.s. not significant, unpaired, two-tailed student’s t-test.

    Techniques Used: Expressing, Cytometry, Functional Assay, Staining, Incubation, Activation Assay, Plasmid Preparation, Construct, Transfection, Two Tailed Test

    Related Articles

    Incubation:

    Article Title: Cdc42 Couples T Cell Receptor Endocytosis to GRAF1-Mediated Tubular Invaginations of the Plasma Membrane.
    Article Snippet: Subsequently, cells were incubated for 30 min at 4 ◦C in serum-free RPMI with 1.5 μg/mL biotinylated anti-CD3ε (clone OKT3, 13-0037-82, eBioscience or clone SK7, 344820, Biolegend, San Diego, CA, USA) and 1 μg/mL non-biotinylated anti-CD28 (28.2, 16-0289, eBioscience) or with 1.5 μg/mL biotinylated isotype control (13-4724-85, eBioscience) and anti-CD28 (1 μg/mL), or with 30 μg/mL biotinylated transferrin (009-060-050, Jackson Immunoresearch) and non-biotinylated anti-CD3ε (1.5 μg/mL, OKT3) and anti-CD28 (1 μg/mL), to allow antibody/Tf binding but not T cell activation and receptor-internalization. .. For non-activating conditions, cells were incubated for 30 min at 4 ◦C in serum-free RPMI with 1.5 μg/mL biotinylated anti-TCRβ (JOVI.1, NBP2-50355B, Novus Biologicals, Littleton, CO, USA). ..

    Article Title: Cdc42 Couples T Cell Receptor Endocytosis to GRAF1-Mediated Tubular Invaginations of the Plasma Membrane
    Article Snippet: Subsequently, cells were incubated for 30 min at 4 °C in serum-free RPMI with 1.5 μg/mL biotinylated anti-CD3ε (clone OKT3, 13-0037-82, eBioscience or clone SK7, 344820, Biolegend, San Diego, CA, USA) and 1 μg/mL non-biotinylated anti-CD28 (28.2, 16-0289, eBioscience) or with 1.5 μg/mL biotinylated isotype control (13-4724-85, eBioscience) and anti-CD28 (1 μg/mL), or with 30 μg/mL biotinylated transferrin (009-060-050, Jackson Immunoresearch) and non-biotinylated anti-CD3ε (1.5 μg/mL, OKT3) and anti-CD28 (1 μg/mL), to allow antibody/Tf binding but not T cell activation and receptor-internalization. .. For non-activating conditions, cells were incubated for 30 min at 4 °C in serum-free RPMI with 1.5 μg/mL biotinylated anti-TCRβ (JOVI.1, NBP2-50355B, Novus Biologicals, Littleton, CO, USA). ..



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    Figure 4. Expression of Cdc42-Q61L selectively impairs internalization of the TCR-CD3 complex. (A) Schematic of the flow-cytometry based internalization assay; cells are labelled at 4 ◦C with a functional <t>biotinylated</t> anti-CD3ε and either (yellow) directly stained with Pacific Blue-streptavidin to measure surface expression of TCR-CD3 complex in resting cells, (blue) activated by incubation at 37 ◦C and stained with Pacific Blue-streptavidin to detect remaining TCR-CD3 at the cell surface after activation-induced internalization, or (red) activated by incubation at 37 ◦C, re-labelled with biotinylated anti-CD3ε and stained with Pacific Blue-streptavidin to detect total surface TCR-CD3 in activated cells. (B) Remaining TCR-CD3 at the cell surface detected by an antibody against CD3ε (clone OKT3) after activation-induced internalization in cells expressing an empty vector, GFP-WT-Cdc42, GFP-Cdc42-Q61L, or GFP-Cdc42-T17N. (C) Surface expression of TCR-CD3 complex in cells expressing the same constructs as in (B). (D) Total surface TCR-CD3 in activated cells transfected as in (B). (E) Internalization of biotinylated Tf detected with Pacific Blue-streptavidin after incubation at 37 ◦C as described for anti-CD3ε in (A), in cells activated by soluble anti-CD3ε and expressing the same constructs as in (B). (F) Surface expression of Tf in cells expressing the same constructs as in (B). (G) Total Tf at the cell surface detected with biotinylated Tf and Pacific Blue-streptavidin in activated cells as in (F). Each data point represents the mean of an individual experiment. Small horizontal lines indicate mean (±SEM), ** p < 0.01, n.s. not significant, unpaired, two-tailed student’s t-test.
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    Image Search Results


    Figure 4. Expression of Cdc42-Q61L selectively impairs internalization of the TCR-CD3 complex. (A) Schematic of the flow-cytometry based internalization assay; cells are labelled at 4 ◦C with a functional biotinylated anti-CD3ε and either (yellow) directly stained with Pacific Blue-streptavidin to measure surface expression of TCR-CD3 complex in resting cells, (blue) activated by incubation at 37 ◦C and stained with Pacific Blue-streptavidin to detect remaining TCR-CD3 at the cell surface after activation-induced internalization, or (red) activated by incubation at 37 ◦C, re-labelled with biotinylated anti-CD3ε and stained with Pacific Blue-streptavidin to detect total surface TCR-CD3 in activated cells. (B) Remaining TCR-CD3 at the cell surface detected by an antibody against CD3ε (clone OKT3) after activation-induced internalization in cells expressing an empty vector, GFP-WT-Cdc42, GFP-Cdc42-Q61L, or GFP-Cdc42-T17N. (C) Surface expression of TCR-CD3 complex in cells expressing the same constructs as in (B). (D) Total surface TCR-CD3 in activated cells transfected as in (B). (E) Internalization of biotinylated Tf detected with Pacific Blue-streptavidin after incubation at 37 ◦C as described for anti-CD3ε in (A), in cells activated by soluble anti-CD3ε and expressing the same constructs as in (B). (F) Surface expression of Tf in cells expressing the same constructs as in (B). (G) Total Tf at the cell surface detected with biotinylated Tf and Pacific Blue-streptavidin in activated cells as in (F). Each data point represents the mean of an individual experiment. Small horizontal lines indicate mean (±SEM), ** p < 0.01, n.s. not significant, unpaired, two-tailed student’s t-test.

    Journal: Cells

    Article Title: Cdc42 Couples T Cell Receptor Endocytosis to GRAF1-Mediated Tubular Invaginations of the Plasma Membrane.

    doi: 10.3390/cells8111388

    Figure Lengend Snippet: Figure 4. Expression of Cdc42-Q61L selectively impairs internalization of the TCR-CD3 complex. (A) Schematic of the flow-cytometry based internalization assay; cells are labelled at 4 ◦C with a functional biotinylated anti-CD3ε and either (yellow) directly stained with Pacific Blue-streptavidin to measure surface expression of TCR-CD3 complex in resting cells, (blue) activated by incubation at 37 ◦C and stained with Pacific Blue-streptavidin to detect remaining TCR-CD3 at the cell surface after activation-induced internalization, or (red) activated by incubation at 37 ◦C, re-labelled with biotinylated anti-CD3ε and stained with Pacific Blue-streptavidin to detect total surface TCR-CD3 in activated cells. (B) Remaining TCR-CD3 at the cell surface detected by an antibody against CD3ε (clone OKT3) after activation-induced internalization in cells expressing an empty vector, GFP-WT-Cdc42, GFP-Cdc42-Q61L, or GFP-Cdc42-T17N. (C) Surface expression of TCR-CD3 complex in cells expressing the same constructs as in (B). (D) Total surface TCR-CD3 in activated cells transfected as in (B). (E) Internalization of biotinylated Tf detected with Pacific Blue-streptavidin after incubation at 37 ◦C as described for anti-CD3ε in (A), in cells activated by soluble anti-CD3ε and expressing the same constructs as in (B). (F) Surface expression of Tf in cells expressing the same constructs as in (B). (G) Total Tf at the cell surface detected with biotinylated Tf and Pacific Blue-streptavidin in activated cells as in (F). Each data point represents the mean of an individual experiment. Small horizontal lines indicate mean (±SEM), ** p < 0.01, n.s. not significant, unpaired, two-tailed student’s t-test.

    Article Snippet: For non-activating conditions, cells were incubated for 30 min at 4 ◦C in serum-free RPMI with 1.5 μg/mL biotinylated anti-TCRβ (JOVI.1, NBP2-50355B, Novus Biologicals, Littleton, CO, USA).

    Techniques: Expressing, Cytometry, Functional Assay, Staining, Incubation, Activation Assay, Plasmid Preparation, Construct, Transfection, Two Tailed Test