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human b cell lymphoma cell lines ramos  (ATCC)


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    Structured Review

    ATCC human b cell lymphoma cell lines ramos
    Human B Cell Lymphoma Cell Lines Ramos, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1435 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+b+cell+lymphoma+cell+line/Ramos/pm42285030-72-0-39
    Average 99 stars, based on 1435 article reviews
    human b cell lymphoma cell lines ramos - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    Planar Chromatography:

    Article Title: TAS05567, a Novel Potent and Selective Spleen Tyrosine Kinase Inhibitor, Abrogates Immunoglobulin-Mediated Autoimmune and Allergic Reactions in Rodent Models.
    Article Snippet: The plates were read using a LabChip EZ Reader (PerkinElmer). .. Detection of B-cell Linker Protein (BLNK), Phospholipase C (PLC) γ2, and Extracellular Signal-regulated Kinase (ERK) Phosphorylation A human B cell lymphoma cell line (Ramos, ATCC CRL-1596) was purchased from the American Type Culture Collection (Manassas, VA, USA) and maintained in Roswell Park Memorial Institute–1640 medium (Sigma-Aldrich) containing 10% fetal bovine serum (FBS). .. Ramos cells (1 × 105 cells/100 μl) were pretreated with test compounds, followed by stimulation with goat F(ab’)2 anti-human IgM (5 μg/ml; Southern Biotech, Birmingham, AL, USA) for 5 min at 37°C.

    Phospho-proteomics:

    Article Title: TAS05567, a Novel Potent and Selective Spleen Tyrosine Kinase Inhibitor, Abrogates Immunoglobulin-Mediated Autoimmune and Allergic Reactions in Rodent Models.
    Article Snippet: The plates were read using a LabChip EZ Reader (PerkinElmer). .. Detection of B-cell Linker Protein (BLNK), Phospholipase C (PLC) γ2, and Extracellular Signal-regulated Kinase (ERK) Phosphorylation A human B cell lymphoma cell line (Ramos, ATCC CRL-1596) was purchased from the American Type Culture Collection (Manassas, VA, USA) and maintained in Roswell Park Memorial Institute–1640 medium (Sigma-Aldrich) containing 10% fetal bovine serum (FBS). .. Ramos cells (1 × 105 cells/100 μl) were pretreated with test compounds, followed by stimulation with goat F(ab’)2 anti-human IgM (5 μg/ml; Southern Biotech, Birmingham, AL, USA) for 5 min at 37°C.

    Expressing:

    Article Title: Epigenome-wide analysis of piRNAs in gene-specific DNA methylation.
    Article Snippet: D ow nl oa de d by [ U ni ve rs ity o f Sa sk at ch ew an L ib ra ry ] at 1 9: 10 2 5 Ja nu ar y 20 15 Ac ce pte d M an us cri pt Pearson's correlation coefficients and p-values were calculated using the SAS statistical software (v9.2) (SAS Institute, Cary, NC). .. Confirmation of PIWIL1, L2, L3, and L4 expression in Farage and MCF-7 cells Farage, a human B cell lymphoma cell line, and MCF-7, a human breast cancer cell line, were purchased from the American Type Culture Collection (ATCC, Manassas, VA). .. Farage cells were maintained in Roswell Park Memorial Institute (RPMI) 1640 media supplemented with 10% fetal bovine serum (FBS) (Invitrogen, Carlsbad, CA).

    other:

    Article Title: Ceramide participates in lysosome-mediated cell death induced by type II anti-CD20 monoclonal antibodies.
    Article Snippet: Although clinical applications have proved the unprecedented success of rituximab in treating a range of CD20positive non-Hodgkin lymphomas (NHLs), a substantial proportion of patients fail to achieve a complete remission (CR) [1,2].. Moreover, tumor relapse is inevitable for most patients [3,4].. Th e limitations of rituximab call for the development of improved treatments for these patients.

    Multiple Displacement Amplification:

    Article Title: Nanoparticle modification of microfluidic cell separation for cancer cell detection and isolation.
    Article Snippet: Cancer is a major health problem in the United States with extremely high mortality.. The detection and isolation of cancer cells are becoming increasingly important for cancer diagnosis.. We describe a microfluidic device modified with silica nanoparticles to enhance the isolation of cancer cells using affinity separation.

    Cell Culture:

    Article Title: Therapeutic peptide delivery via aptamer-displaying, disulfide-linked peptide amphiphile micelles
    Article Snippet: Peptide amphiphile micelles (PAMs) are a powerful platform technology for improving the delivery of therapeutic and prophylactic peptides.. While previous research has shown aptamer-displaying PAMs enhance cell association, transportation to intracellular targets still remains a substantial hurdle for these biomaterials.. In this article, we detail our efforts to address this challenge through the creation of disulfidelinked peptide amphiphile (PAs).



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    ST6 OE CAR-T cells exhibited effective tumoricidal activity in the presence of Gal-3 and evaded Gal-3-induced expression of IL-5, which compromised anti-tumor efficacy. Day 10-expanded T cells, CAR-T cells, and ST6 OE CAR-T cells were incubated with Gal-3 low <t>Raji-luc</t> + cells or Gal-3 high SUDHL-6-luc + cells at effector:target (E:T) ratios of 20:1. Raji cell cytotoxicity was evaluated (a) without rhGal-3 or (b) with rhGal-3, and (c) Gal-3 high SUDHL-6 cell cytotoxicity was examined without exogenous rhGal-3. Data are presented from n = 4 independent donors and analyzed using a two-way repeated-measures ANOVA with Sidak’s multiple-comparisons test, with ** p < 0.01, * p < 0.05. (d) Human cytokine proteome profiling of supernatants from Day 10-expanded T cells, CAR-T cells, and ST6 OE CAR-T cells incubated with rhGal-3 for 16h revealed a marked upregulation of IL-5 (red hatched box) in CAR-T cells that was absent in ST6 OE CAR-T cells. (e) Arrays were repeated 4 times and graphed as Relative Optical Density (Mean ± SEM). Intracellular IL-5 expression was assessed by flow cytometry in control Day 10-expanded T cells, CAR-T cells and ST6 OE CAR-T cells after rhGal-3 incubation for 16h and mean ± SEM fold change from n = 4 independent donors was graphed (f) (* p < 0.05). Statistical significance was determined using a Mann–Whitney U test. CAR-T cells and ST6 OE CAR-T cells were incubated with (g) Gal-3 low Raji-luc + cells or (h) Gal-3 high SUDHL6-luc + at E:T ratios of 20:1 (** p <0.01, *** p <0.001). Statistical significance was determined using two-way repeated-measures ANOVA with Sidak’s multiple-comparisons test.
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    Roles of ISOIM/siBTK@Exosome on T cells activation and macrophage polarization. A, Experimental scheme for the co-culture of stimulated CD3 + T cells <t>and</t> <t>treated</t> <t>SU-DHL-4</t> cells; B-C, Representative images (B) and corresponding quantitative analysis (C) showing the percentages of CD69 + CD4 + T cells and CD69 + CD8 + T cells in the coculture system; D, Experimental scheme for the co-culture of stimulated peritoneal macrophages and treated SU-DHL-4 cells; E-F, Representative images (E) and corresponding quantitative analysis (F) showing the percentages of M2 macrophages in the coculture system. ∗P < 0.05; ∗∗P < 0.01.
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    Roles of ISOIM/siBTK@Exosome on T cells activation and macrophage polarization. A, Experimental scheme for the co-culture of stimulated CD3 + T cells <t>and</t> <t>treated</t> <t>SU-DHL-4</t> cells; B-C, Representative images (B) and corresponding quantitative analysis (C) showing the percentages of CD69 + CD4 + T cells and CD69 + CD8 + T cells in the coculture system; D, Experimental scheme for the co-culture of stimulated peritoneal macrophages and treated SU-DHL-4 cells; E-F, Representative images (E) and corresponding quantitative analysis (F) showing the percentages of M2 macrophages in the coculture system. ∗P < 0.05; ∗∗P < 0.01.
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    Roles of ISOIM/siBTK@Exosome on T cells activation and macrophage polarization. A, Experimental scheme for the co-culture of stimulated CD3 + T cells <t>and</t> <t>treated</t> <t>SU-DHL-4</t> cells; B-C, Representative images (B) and corresponding quantitative analysis (C) showing the percentages of CD69 + CD4 + T cells and CD69 + CD8 + T cells in the coculture system; D, Experimental scheme for the co-culture of stimulated peritoneal macrophages and treated SU-DHL-4 cells; E-F, Representative images (E) and corresponding quantitative analysis (F) showing the percentages of M2 macrophages in the coculture system. ∗P < 0.05; ∗∗P < 0.01.
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    ST6 OE CAR-T cells exhibited effective tumoricidal activity in the presence of Gal-3 and evaded Gal-3-induced expression of IL-5, which compromised anti-tumor efficacy. Day 10-expanded T cells, CAR-T cells, and ST6 OE CAR-T cells were incubated with Gal-3 low Raji-luc + cells or Gal-3 high SUDHL-6-luc + cells at effector:target (E:T) ratios of 20:1. Raji cell cytotoxicity was evaluated (a) without rhGal-3 or (b) with rhGal-3, and (c) Gal-3 high SUDHL-6 cell cytotoxicity was examined without exogenous rhGal-3. Data are presented from n = 4 independent donors and analyzed using a two-way repeated-measures ANOVA with Sidak’s multiple-comparisons test, with ** p < 0.01, * p < 0.05. (d) Human cytokine proteome profiling of supernatants from Day 10-expanded T cells, CAR-T cells, and ST6 OE CAR-T cells incubated with rhGal-3 for 16h revealed a marked upregulation of IL-5 (red hatched box) in CAR-T cells that was absent in ST6 OE CAR-T cells. (e) Arrays were repeated 4 times and graphed as Relative Optical Density (Mean ± SEM). Intracellular IL-5 expression was assessed by flow cytometry in control Day 10-expanded T cells, CAR-T cells and ST6 OE CAR-T cells after rhGal-3 incubation for 16h and mean ± SEM fold change from n = 4 independent donors was graphed (f) (* p < 0.05). Statistical significance was determined using a Mann–Whitney U test. CAR-T cells and ST6 OE CAR-T cells were incubated with (g) Gal-3 low Raji-luc + cells or (h) Gal-3 high SUDHL6-luc + at E:T ratios of 20:1 (** p <0.01, *** p <0.001). Statistical significance was determined using two-way repeated-measures ANOVA with Sidak’s multiple-comparisons test.

    Journal: Frontiers in Immunology

    Article Title: Glycoengineering CAR-T cells to overcome galectin-3-mediated immunosuppression

    doi: 10.3389/fimmu.2026.1766555

    Figure Lengend Snippet: ST6 OE CAR-T cells exhibited effective tumoricidal activity in the presence of Gal-3 and evaded Gal-3-induced expression of IL-5, which compromised anti-tumor efficacy. Day 10-expanded T cells, CAR-T cells, and ST6 OE CAR-T cells were incubated with Gal-3 low Raji-luc + cells or Gal-3 high SUDHL-6-luc + cells at effector:target (E:T) ratios of 20:1. Raji cell cytotoxicity was evaluated (a) without rhGal-3 or (b) with rhGal-3, and (c) Gal-3 high SUDHL-6 cell cytotoxicity was examined without exogenous rhGal-3. Data are presented from n = 4 independent donors and analyzed using a two-way repeated-measures ANOVA with Sidak’s multiple-comparisons test, with ** p < 0.01, * p < 0.05. (d) Human cytokine proteome profiling of supernatants from Day 10-expanded T cells, CAR-T cells, and ST6 OE CAR-T cells incubated with rhGal-3 for 16h revealed a marked upregulation of IL-5 (red hatched box) in CAR-T cells that was absent in ST6 OE CAR-T cells. (e) Arrays were repeated 4 times and graphed as Relative Optical Density (Mean ± SEM). Intracellular IL-5 expression was assessed by flow cytometry in control Day 10-expanded T cells, CAR-T cells and ST6 OE CAR-T cells after rhGal-3 incubation for 16h and mean ± SEM fold change from n = 4 independent donors was graphed (f) (* p < 0.05). Statistical significance was determined using a Mann–Whitney U test. CAR-T cells and ST6 OE CAR-T cells were incubated with (g) Gal-3 low Raji-luc + cells or (h) Gal-3 high SUDHL6-luc + at E:T ratios of 20:1 (** p <0.01, *** p <0.001). Statistical significance was determined using two-way repeated-measures ANOVA with Sidak’s multiple-comparisons test.

    Article Snippet: Human B-lymphoma Raji cell line expressing luciferase (Raji-Luc + ) purchased from the ATCC (Manassas, VA).

    Techniques: Activity Assay, Expressing, Incubation, Flow Cytometry, Control, MANN-WHITNEY

    ST6 OE CAR-T cells exhibited potent in vivo anti-tumor activity and persisted longer in vivo than conventional CAR-T cells. Using a DLBCL xenograft model (a) , NSG mice were inoculated with Raji-luc + cells and, after 7 days, treated with media (control), Day 10-expanded T cells, CAR-T cells, or ST6 OE CAR-T cells. Tumor growth in NSG mice was monitored weekly by in vivo BL imaging system (b) , and BLI measurements reflecting tumor burden from respective groups were graphed as shown (n = 9 mice per group) (** p < 0.01) (c) . Xenografted mouse survival data were graphed as shown (Gehan-Breslow-Wilcoxon test – ** p = 0.0106) (d) , and flow cytometry of CAR + T cells isolated from xenografted mouse spleens expressed as Mean ± SEM were graphed as shown (Mann–Whitney U test- * p <0.05) (e) .

    Journal: Frontiers in Immunology

    Article Title: Glycoengineering CAR-T cells to overcome galectin-3-mediated immunosuppression

    doi: 10.3389/fimmu.2026.1766555

    Figure Lengend Snippet: ST6 OE CAR-T cells exhibited potent in vivo anti-tumor activity and persisted longer in vivo than conventional CAR-T cells. Using a DLBCL xenograft model (a) , NSG mice were inoculated with Raji-luc + cells and, after 7 days, treated with media (control), Day 10-expanded T cells, CAR-T cells, or ST6 OE CAR-T cells. Tumor growth in NSG mice was monitored weekly by in vivo BL imaging system (b) , and BLI measurements reflecting tumor burden from respective groups were graphed as shown (n = 9 mice per group) (** p < 0.01) (c) . Xenografted mouse survival data were graphed as shown (Gehan-Breslow-Wilcoxon test – ** p = 0.0106) (d) , and flow cytometry of CAR + T cells isolated from xenografted mouse spleens expressed as Mean ± SEM were graphed as shown (Mann–Whitney U test- * p <0.05) (e) .

    Article Snippet: Human B-lymphoma Raji cell line expressing luciferase (Raji-Luc + ) purchased from the ATCC (Manassas, VA).

    Techniques: In Vivo, Activity Assay, Control, Imaging, Flow Cytometry, Isolation, MANN-WHITNEY

    Roles of ISOIM/siBTK@Exosome on T cells activation and macrophage polarization. A, Experimental scheme for the co-culture of stimulated CD3 + T cells and treated SU-DHL-4 cells; B-C, Representative images (B) and corresponding quantitative analysis (C) showing the percentages of CD69 + CD4 + T cells and CD69 + CD8 + T cells in the coculture system; D, Experimental scheme for the co-culture of stimulated peritoneal macrophages and treated SU-DHL-4 cells; E-F, Representative images (E) and corresponding quantitative analysis (F) showing the percentages of M2 macrophages in the coculture system. ∗P < 0.05; ∗∗P < 0.01.

    Journal: Materials Today Bio

    Article Title: Tumor-homing exosomes enable targeted delivery of siRNA and isoimperatorin for overcoming BTK inhibitor resistance in DLBCL

    doi: 10.1016/j.mtbio.2025.102267

    Figure Lengend Snippet: Roles of ISOIM/siBTK@Exosome on T cells activation and macrophage polarization. A, Experimental scheme for the co-culture of stimulated CD3 + T cells and treated SU-DHL-4 cells; B-C, Representative images (B) and corresponding quantitative analysis (C) showing the percentages of CD69 + CD4 + T cells and CD69 + CD8 + T cells in the coculture system; D, Experimental scheme for the co-culture of stimulated peritoneal macrophages and treated SU-DHL-4 cells; E-F, Representative images (E) and corresponding quantitative analysis (F) showing the percentages of M2 macrophages in the coculture system. ∗P < 0.05; ∗∗P < 0.01.

    Article Snippet: Human B Lymphoma cell line SU-DHL-4 (#CRL-2957, ATCC, USA) and OCL-Ly8 (#JLC- G14773 , Gelatins biological reagent Co., LTD, Jiangxi, China) were cultured in the RPMI-1640 medium with an additional adding of 10 % FBS, penicillin (100 U/mL) and streptomycin (100 μg/mL) in an incubator of 5 % CO 2 at 37 °C.

    Techniques: Activation Assay, Co-Culture Assay