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Becton Dickinson polystyrene flow cytometry tubes bd falcon
Polystyrene Flow Cytometry Tubes Bd Falcon, supplied by Becton Dickinson, 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/polystyrene+flow+cytometry+tubes/polystyrene+flow+cytometry+tubes+bd+falcon/pm36930397-41-6-10
Average 90 stars, based on 1 article reviews
polystyrene flow cytometry tubes bd falcon - by Bioz Stars, 2026-11
90/100 stars

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Related Articles

Flow Cytometry:

Article Title: Structure-property relationships of amphiphilic nanoparticles that penetrate or fuse lipid membranes
Article Snippet: Z-stacks were collected using an optical slice thickness of 1 μm, and images were analyzed with Zeiss LSM software. .. Flow cytometry Flow cytometry samples were prepared in 96-well round-bottom plates (BD) or polystyrene flow cytometry tubes (BD Falcon). ..

Article Title: Structure-property relationships of amphiphilic nanoparticles that penetrate or fuse lipid membranes
Article Snippet: Z-stacks were collected using an optical slice thickness of 1 μm, and images were analyzed with Zeiss LSM software. .. Flow cytometry samples were prepared in 96-well round-bottom plates (BD) or polystyrene flow cytometry tubes (BD Falcon). ..

Article Title: Establishment of a healthy human range for the whole blood 'OX40' assay for the detection of antigen-specific CD4+ T cells by flow cytometry.
Article Snippet: Abbreviations: VZV – Varicella-Zoster Virus, EBV – Epstein-Barr Virus, CMV – Cytomegalovirus, CFSE Carboxyfluorescein succinimidyl ester, REC – Research ethics committee, PHA – Phytohaemagluttinin, HFF – Human foreskin fibroblast, PBMC – Peripheral blood mononuclear cell, FIFluorescent intensity, CVID – Common Variable Immunodeficiency, IVIG – Intravenous Immunoglobulin, XIAP – X-linked inhibitor of apoptosis.

Article Title: CD8-positive memory T cells in tumor-draining lymph nodes of patients with breast cancer
Article Snippet: To determine the number of viable cells, the Trypan Blue dye (Biosera, France) exclusion test was used. .. Then cells at a concentration of 250 × 10 3 in 50 μl 1 × PBS were distributed in round-bottomed polystyrene flow cytometry tubes (BD Biosciences, USA) for further analysis. .. To determine the phenotype of memory T cell subsets, we used the following anti-human antibodies: FITC-anti-CCR7 (3D12), PE-anti-CD95 (Dx2), APC-conjugated anti-CD45RO (UCHL1), and PerCP anti-CD8 (Sk1), and their respective isotype controls: FITC-conjugated mouse IgG2a, PE-conjugated mouse IgG1, APC-conjugated mouse IgG2a, and PerCP-conjugated mouse IgG1 (all from BD Biosciences, USA).

Article Title: Structure–Property Relationships of Amphiphilic Nanoparticles That Penetrate or Fuse Lipid Membranes
Article Snippet: .. Flow cytometry samples were prepared in 96-well round-bottom plates (BD) or polystyrene flow cytometry tubes (BD Falcon). ..

Article Title: Taurine improves the wound healing process in cutaneous leishmaniasis in mice model, based on stereological parameters
Article Snippet: .. The cell suspension was transferred into polystyrene flow cytometry tubes (BD Falcon Company, USA). .. We performed data acquisition and analysis, with a FACSCalibur flow cytometer (Becton-Dickinson, San Jose, USA) and the cell Quest Pro software.

other:

Article Title: Methods and systems for determining the distribution of radiation dose and response
Article Snippet: The cells were resuspended in 1 mL of MOPS buffer containing EuTc (Sigma, catalog nos.

Article Title: Method of overcoming therapeutic limitations of non-uniform distribution of radiopharmaceuticals and chemotherapy drugs
Article Snippet: The cells were resuspended in 1 mL of MOPS buffer containing EuTc (Sigma, catalog nos.

Modification:

Article Title: Establishment of a healthy human range for the whole blood 'OX40' assay for the detection of antigen-specific CD4+ T cells by flow cytometry.
Article Snippet: Abbreviations: VZV – Varicella-Zoster Virus, EBV – Epstein-Barr Virus, CMV – Cytomegalovirus, CFSE Carboxyfluorescein succinimidyl ester, REC – Research ethics committee, PHA – Phytohaemagluttinin, HFF – Human foreskin fibroblast, PBMC – Peripheral blood mononuclear cell, FIFluorescent intensity, CVID – Common Variable Immunodeficiency, IVIG – Intravenous Immunoglobulin, XIAP – X-linked inhibitor of apoptosis.

Sterility:

Article Title: Establishment of a healthy human range for the whole blood 'OX40' assay for the detection of antigen-specific CD4+ T cells by flow cytometry.
Article Snippet: Abbreviations: VZV – Varicella-Zoster Virus, EBV – Epstein-Barr Virus, CMV – Cytomegalovirus, CFSE Carboxyfluorescein succinimidyl ester, REC – Research ethics committee, PHA – Phytohaemagluttinin, HFF – Human foreskin fibroblast, PBMC – Peripheral blood mononuclear cell, FIFluorescent intensity, CVID – Common Variable Immunodeficiency, IVIG – Intravenous Immunoglobulin, XIAP – X-linked inhibitor of apoptosis.

Concentration Assay:

Article Title: CD8-positive memory T cells in tumor-draining lymph nodes of patients with breast cancer
Article Snippet: To determine the number of viable cells, the Trypan Blue dye (Biosera, France) exclusion test was used. .. Then cells at a concentration of 250 × 10 3 in 50 μl 1 × PBS were distributed in round-bottomed polystyrene flow cytometry tubes (BD Biosciences, USA) for further analysis. .. To determine the phenotype of memory T cell subsets, we used the following anti-human antibodies: FITC-anti-CCR7 (3D12), PE-anti-CD95 (Dx2), APC-conjugated anti-CD45RO (UCHL1), and PerCP anti-CD8 (Sk1), and their respective isotype controls: FITC-conjugated mouse IgG2a, PE-conjugated mouse IgG1, APC-conjugated mouse IgG2a, and PerCP-conjugated mouse IgG1 (all from BD Biosciences, USA).

Suspension:

Article Title: Taurine improves the wound healing process in cutaneous leishmaniasis in mice model, based on stereological parameters
Article Snippet: .. The cell suspension was transferred into polystyrene flow cytometry tubes (BD Falcon Company, USA). .. We performed data acquisition and analysis, with a FACSCalibur flow cytometer (Becton-Dickinson, San Jose, USA) and the cell Quest Pro software.



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Fisher Scientific filter top polystyrene flow cytometry tube
A: Schematic overview of the screening approach. hiPSC-derived CD34 + hemogenic endothelial cells were differentiated towards ProT cells for 14 days in a stroma-free protocol . At iT day 14 cells were harvested and replated into a 384 well plate and exposed to a small molecule library. After 7 days cells were stained with anti CD56, anti CD4, anti CD7 with 7-AAD and Calcein Violet viability dyes. Scale bar indicates 20 µm. B: Primary screening results. 5 hits were identified when a Z-score threshold of 1 was applied. C: Hit validation, bar graphs depicting mean percentage of CD4 + cells out of CD45 + population on iT day 28 in hiPSC line EZH1 mut/wt (screening line), BCH1157 and BCH1566. Error bars depict SEM of replicate wells, one way ANOVA comparison against DMSO. E: Exemplary flow <t>cytometry</t> plots on iT day 28 demonstrating an increased proportion of CD4 + CD8 + DP cells after GNF351 treatment in BCH1157 hiPSC-derived ProT cells. F: Mean values plotted from two independent experiments with either continuous drug treatment (solid circles) or one time drug exposure (open circles). SEM of technical replicates is indicated by blue shading. Two-way ANOVA with Dunnett’s multiple comparison test against respective untreated cells.
Filter Top Polystyrene Flow Cytometry Tube, supplied by Fisher Scientific, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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A: Schematic overview of the screening approach. hiPSC-derived CD34 + hemogenic endothelial cells were differentiated towards ProT cells for 14 days in a stroma-free protocol . At iT day 14 cells were harvested and replated into a 384 well plate and exposed to a small molecule library. After 7 days cells were stained with anti CD56, anti CD4, anti CD7 with 7-AAD and Calcein Violet viability dyes. Scale bar indicates 20 µm. B: Primary screening results. 5 hits were identified when a Z-score threshold of 1 was applied. C: Hit validation, bar graphs depicting mean percentage of CD4 + cells out of CD45 + population on iT day 28 in hiPSC line EZH1 mut/wt (screening line), BCH1157 and BCH1566. Error bars depict SEM of replicate wells, one way ANOVA comparison against DMSO. E: Exemplary flow <t>cytometry</t> plots on iT day 28 demonstrating an increased proportion of CD4 + CD8 + DP cells after GNF351 treatment in BCH1157 hiPSC-derived ProT cells. F: Mean values plotted from two independent experiments with either continuous drug treatment (solid circles) or one time drug exposure (open circles). SEM of technical replicates is indicated by blue shading. Two-way ANOVA with Dunnett’s multiple comparison test against respective untreated cells.
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A: Schematic overview of the screening approach. hiPSC-derived CD34 + hemogenic endothelial cells were differentiated towards ProT cells for 14 days in a stroma-free protocol . At iT day 14 cells were harvested and replated into a 384 well plate and exposed to a small molecule library. After 7 days cells were stained with anti CD56, anti CD4, anti CD7 with 7-AAD and Calcein Violet viability dyes. Scale bar indicates 20 µm. B: Primary screening results. 5 hits were identified when a Z-score threshold of 1 was applied. C: Hit validation, bar graphs depicting mean percentage of CD4 + cells out of CD45 + population on iT day 28 in hiPSC line EZH1 mut/wt (screening line), BCH1157 and BCH1566. Error bars depict SEM of replicate wells, one way ANOVA comparison against DMSO. E: Exemplary flow <t>cytometry</t> plots on iT day 28 demonstrating an increased proportion of CD4 + CD8 + DP cells after GNF351 treatment in BCH1157 hiPSC-derived ProT cells. F: Mean values plotted from two independent experiments with either continuous drug treatment (solid circles) or one time drug exposure (open circles). SEM of technical replicates is indicated by blue shading. Two-way ANOVA with Dunnett’s multiple comparison test against respective untreated cells.
Polystyrene Round Bottom Tubes For Flow Cytometry, supplied by Corning Life Sciences, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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A: Schematic overview of the screening approach. hiPSC-derived CD34 + hemogenic endothelial cells were differentiated towards ProT cells for 14 days in a stroma-free protocol . At iT day 14 cells were harvested and replated into a 384 well plate and exposed to a small molecule library. After 7 days cells were stained with anti CD56, anti CD4, anti CD7 with 7-AAD and Calcein Violet viability dyes. Scale bar indicates 20 µm. B: Primary screening results. 5 hits were identified when a Z-score threshold of 1 was applied. C: Hit validation, bar graphs depicting mean percentage of CD4 + cells out of CD45 + population on iT day 28 in hiPSC line EZH1 mut/wt (screening line), BCH1157 and BCH1566. Error bars depict SEM of replicate wells, one way ANOVA comparison against DMSO. E: Exemplary flow <t>cytometry</t> plots on iT day 28 demonstrating an increased proportion of CD4 + CD8 + DP cells after GNF351 treatment in BCH1157 hiPSC-derived ProT cells. F: Mean values plotted from two independent experiments with either continuous drug treatment (solid circles) or one time drug exposure (open circles). SEM of technical replicates is indicated by blue shading. Two-way ANOVA with Dunnett’s multiple comparison test against respective untreated cells.
Polystyrene Flow Cytometry Tube, supplied by Corning Life Sciences, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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A: Schematic overview of the screening approach. hiPSC-derived CD34 + hemogenic endothelial cells were differentiated towards ProT cells for 14 days in a stroma-free protocol . At iT day 14 cells were harvested and replated into a 384 well plate and exposed to a small molecule library. After 7 days cells were stained with anti CD56, anti CD4, anti CD7 with 7-AAD and Calcein Violet viability dyes. Scale bar indicates 20 µm. B: Primary screening results. 5 hits were identified when a Z-score threshold of 1 was applied. C: Hit validation, bar graphs depicting mean percentage of CD4 + cells out of CD45 + population on iT day 28 in hiPSC line EZH1 mut/wt (screening line), BCH1157 and BCH1566. Error bars depict SEM of replicate wells, one way ANOVA comparison against DMSO. E: Exemplary flow <t>cytometry</t> plots on iT day 28 demonstrating an increased proportion of CD4 + CD8 + DP cells after GNF351 treatment in BCH1157 hiPSC-derived ProT cells. F: Mean values plotted from two independent experiments with either continuous drug treatment (solid circles) or one time drug exposure (open circles). SEM of technical replicates is indicated by blue shading. Two-way ANOVA with Dunnett’s multiple comparison test against respective untreated cells.
Polystyrene Flow Cytometry Tubes Bd Falcon, supplied by Becton Dickinson, 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/polystyrene+flow+cytometry+tubes/polystyrene+flow+cytometry+tubes+bd+falcon/pm36930397-41-6-10
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A: Schematic overview of the screening approach. hiPSC-derived CD34 + hemogenic endothelial cells were differentiated towards ProT cells for 14 days in a stroma-free protocol . At iT day 14 cells were harvested and replated into a 384 well plate and exposed to a small molecule library. After 7 days cells were stained with anti CD56, anti CD4, anti CD7 with 7-AAD and Calcein Violet viability dyes. Scale bar indicates 20 µm. B: Primary screening results. 5 hits were identified when a Z-score threshold of 1 was applied. C: Hit validation, bar graphs depicting mean percentage of CD4 + cells out of CD45 + population on iT day 28 in hiPSC line EZH1 mut/wt (screening line), BCH1157 and BCH1566. Error bars depict SEM of replicate wells, one way ANOVA comparison against DMSO. E: Exemplary flow <t>cytometry</t> plots on iT day 28 demonstrating an increased proportion of CD4 + CD8 + DP cells after GNF351 treatment in BCH1157 hiPSC-derived ProT cells. F: Mean values plotted from two independent experiments with either continuous drug treatment (solid circles) or one time drug exposure (open circles). SEM of technical replicates is indicated by blue shading. Two-way ANOVA with Dunnett’s multiple comparison test against respective untreated cells.
Polystyrene Flow Cytometry Tubes, supplied by Becton Dickinson, 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/polystyrene+flow+cytometry+tubes/polystyrene+flow+cytometry+tubes/pm24520004-34-26-30
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A: Schematic overview of the screening approach. hiPSC-derived CD34 + hemogenic endothelial cells were differentiated towards ProT cells for 14 days in a stroma-free protocol . At iT day 14 cells were harvested and replated into a 384 well plate and exposed to a small molecule library. After 7 days cells were stained with anti CD56, anti CD4, anti CD7 with 7-AAD and Calcein Violet viability dyes. Scale bar indicates 20 µm. B: Primary screening results. 5 hits were identified when a Z-score threshold of 1 was applied. C: Hit validation, bar graphs depicting mean percentage of CD4 + cells out of CD45 + population on iT day 28 in hiPSC line EZH1 mut/wt (screening line), BCH1157 and BCH1566. Error bars depict SEM of replicate wells, one way ANOVA comparison against DMSO. E: Exemplary flow <t>cytometry</t> plots on iT day 28 demonstrating an increased proportion of CD4 + CD8 + DP cells after GNF351 treatment in BCH1157 hiPSC-derived ProT cells. F: Mean values plotted from two independent experiments with either continuous drug treatment (solid circles) or one time drug exposure (open circles). SEM of technical replicates is indicated by blue shading. Two-way ANOVA with Dunnett’s multiple comparison test against respective untreated cells.
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A: Schematic overview of the screening approach. hiPSC-derived CD34 + hemogenic endothelial cells were differentiated towards ProT cells for 14 days in a stroma-free protocol . At iT day 14 cells were harvested and replated into a 384 well plate and exposed to a small molecule library. After 7 days cells were stained with anti CD56, anti CD4, anti CD7 with 7-AAD and Calcein Violet viability dyes. Scale bar indicates 20 µm. B: Primary screening results. 5 hits were identified when a Z-score threshold of 1 was applied. C: Hit validation, bar graphs depicting mean percentage of CD4 + cells out of CD45 + population on iT day 28 in hiPSC line EZH1 mut/wt (screening line), BCH1157 and BCH1566. Error bars depict SEM of replicate wells, one way ANOVA comparison against DMSO. E: Exemplary flow cytometry plots on iT day 28 demonstrating an increased proportion of CD4 + CD8 + DP cells after GNF351 treatment in BCH1157 hiPSC-derived ProT cells. F: Mean values plotted from two independent experiments with either continuous drug treatment (solid circles) or one time drug exposure (open circles). SEM of technical replicates is indicated by blue shading. Two-way ANOVA with Dunnett’s multiple comparison test against respective untreated cells.

Journal: bioRxiv

Article Title: Efficient Generation of Functional TCRαβ + Cytotoxic T Cells from hiPSCs via Small-Molecule Modulation

doi: 10.64898/2026.03.31.715684

Figure Lengend Snippet: A: Schematic overview of the screening approach. hiPSC-derived CD34 + hemogenic endothelial cells were differentiated towards ProT cells for 14 days in a stroma-free protocol . At iT day 14 cells were harvested and replated into a 384 well plate and exposed to a small molecule library. After 7 days cells were stained with anti CD56, anti CD4, anti CD7 with 7-AAD and Calcein Violet viability dyes. Scale bar indicates 20 µm. B: Primary screening results. 5 hits were identified when a Z-score threshold of 1 was applied. C: Hit validation, bar graphs depicting mean percentage of CD4 + cells out of CD45 + population on iT day 28 in hiPSC line EZH1 mut/wt (screening line), BCH1157 and BCH1566. Error bars depict SEM of replicate wells, one way ANOVA comparison against DMSO. E: Exemplary flow cytometry plots on iT day 28 demonstrating an increased proportion of CD4 + CD8 + DP cells after GNF351 treatment in BCH1157 hiPSC-derived ProT cells. F: Mean values plotted from two independent experiments with either continuous drug treatment (solid circles) or one time drug exposure (open circles). SEM of technical replicates is indicated by blue shading. Two-way ANOVA with Dunnett’s multiple comparison test against respective untreated cells.

Article Snippet: The cells were then filtered through a filter-top polystyrene flow cytometry tube (Fisher Scientific, #08-771-23), washed with flow cytometry buffer (PBS + 2% FBS + antibiotics), and centrifuged at 300xg for 5 minutes followed by antibody staining and flow cytometric analysis for expression of CD45 and CD19.

Techniques: Derivative Assay, Staining, Biomarker Discovery, Comparison, Flow Cytometry