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untouched splenic cd8 t splenocytes  (Miltenyi Biotec)


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    Structured Review

    Miltenyi Biotec untouched splenic cd8 t splenocytes
    Untouched Splenic Cd8 T Splenocytes, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 97/100, based on 629 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/splenocytes/CD8a%2B+T+Cell+Isolation+Kit%2C+mouse/10__1158_slash_1535___7163__mct___25___1488-143-7-26
    Average 97 stars, based on 629 article reviews
    untouched splenic cd8 t splenocytes - by Bioz Stars, 2026-09
    97/100 stars

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    Related Articles

    Incubation:

    Article Title: Xist Deletion in B Cells Results in Systemic Lupus Erythematosus Phenotypes
    Article Snippet: Briefly, spleens were mechanically homogenized and splenocytes were incubated with Biotin anti-mouse CD23 (Biolegend 101604 clone B3B4). .. Splenocytes were then incubated with Streptavidin MicroBeads (Miltenyi 130-048-101) and passed through a magnetic LS Column (Miltenyi 130-042-401). .. B cell activation was induced using 24-hour incubation with the Tlr9 agonist CpG (Invivogen tlrl-1826-1).

    Isolation:

    Article Title: Targeting highly attenuated IL-18 to PD-1 for enhanced anti-tumor activity
    Article Snippet: .. Splenocytes were isolated, and tumors were dissociated using the mouse tumor dissociation kit (Miltenyi Biotec, Cat No: 130-096-730) and gentleMACSTM Dissociator (Miltenyi Biotec, Cat No: 130-093-235). ..

    Article Title: Aryl hydrocarbon receptor ligands drive pancreatic cancer initiation and progression through pro-tumorigenic T cell polarization
    Article Snippet: Although smoking is a risk factor for pancreatic adenocarcinoma (PDAC), the underlying mechanism promoting tumorigenesis and progression are unknown.. Here, we show that aryl hydrocarbon receptor ligands found in cigarette smoke, like the carcinogen 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), promote pancreatic dysplasia and PDAC progression in a mouse model of this disease.. This effect is mediated by AhR activation in CD4+ T cells, leading to their polarization to interleukin-22 (IL22) producing TH22 cells and to regulatory T cells (Treg) accumulation, ultimately driving a blunted CD8+ T cell effector response.

    Article Title: Aryl Hydrocarbon Receptor Ligands Drive Pancreatic Cancer Initiation and Progression through Protumorigenic T-cell Polarization
    Article Snippet: .. Naïve CD4 + T cells were purified by magnetic cell separation from total splenocytes isolated from murine spleens (Miltenyi Biotec, #130-104-453) or Gift of Life donor spleens (Miltenyi Biotec, #130-094-131) in an isolation buffer [1× PBS, 0.5% BSA, and 2 mmol/L EDTA (Lonza, #51201)]. .. Naïve CD4 + T cells were stimulated in Iscove’s Modified Dulbecco’s Medium (Gibco, #12440-053) supplemented with 10% FBS, 50 μmol/L β-mercaptoethanol (Bio-Rad, #1610710), and 1× penicillin–streptomycin with plate-bound anti-CD3 (2 μg/mL, mouse – BioLegend #100238, human – BioLegend #317326) and soluble anti-CD28 (0.5 μg/mL, mouse – BioLegend #102116, human – BioLegend #302934) for 5 days under the following conditions: Th0 (media alone), Th1 [5 ng/mL IL2 (mouse – BioLegend #575402) and 10 ng/mL IL12 (mouse BioLegend #577004)], and Th22 [30 ng/mL IL6 (mouse – BioLegend #575702 and human – BioLegend #570802), 10 ng/mL IL1β (mouse – BioLegend #575102 and human – BioLegend #579402), 20 ng/mL IL23 (mouse – BioLegend #589002 and human – BioLegend #574102), and 10 μmol/L galunisertib (Tocris #6956)].

    In Vitro:

    Article Title: Aryl hydrocarbon receptor ligands drive pancreatic cancer initiation and progression through pro-tumorigenic T cell polarization
    Article Snippet: Although smoking is a risk factor for pancreatic adenocarcinoma (PDAC), the underlying mechanism promoting tumorigenesis and progression are unknown.. Here, we show that aryl hydrocarbon receptor ligands found in cigarette smoke, like the carcinogen 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), promote pancreatic dysplasia and PDAC progression in a mouse model of this disease.. This effect is mediated by AhR activation in CD4+ T cells, leading to their polarization to interleukin-22 (IL22) producing TH22 cells and to regulatory T cells (Treg) accumulation, ultimately driving a blunted CD8+ T cell effector response.

    Purification:

    Article Title: Aryl hydrocarbon receptor ligands drive pancreatic cancer initiation and progression through pro-tumorigenic T cell polarization
    Article Snippet: Although smoking is a risk factor for pancreatic adenocarcinoma (PDAC), the underlying mechanism promoting tumorigenesis and progression are unknown.. Here, we show that aryl hydrocarbon receptor ligands found in cigarette smoke, like the carcinogen 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), promote pancreatic dysplasia and PDAC progression in a mouse model of this disease.. This effect is mediated by AhR activation in CD4+ T cells, leading to their polarization to interleukin-22 (IL22) producing TH22 cells and to regulatory T cells (Treg) accumulation, ultimately driving a blunted CD8+ T cell effector response.

    Article Title: The CCL17-CCR4 axis is critical for mutant STAT6-mediated microenvironmental remodelling and therapeutic resistance in Relapsed/Refractory Diffuse Large B-cell Lymphoma
    Article Snippet: .. Following dissociation, CD4+ T cells were purified from splenocytes (Miltenyi, 130- 104-454), as per manufacturer protocol. ..

    Article Title: Aryl Hydrocarbon Receptor Ligands Drive Pancreatic Cancer Initiation and Progression through Protumorigenic T-cell Polarization
    Article Snippet: .. Naïve CD4 + T cells were purified by magnetic cell separation from total splenocytes isolated from murine spleens (Miltenyi Biotec, #130-104-453) or Gift of Life donor spleens (Miltenyi Biotec, #130-094-131) in an isolation buffer [1× PBS, 0.5% BSA, and 2 mmol/L EDTA (Lonza, #51201)]. .. Naïve CD4 + T cells were stimulated in Iscove’s Modified Dulbecco’s Medium (Gibco, #12440-053) supplemented with 10% FBS, 50 μmol/L β-mercaptoethanol (Bio-Rad, #1610710), and 1× penicillin–streptomycin with plate-bound anti-CD3 (2 μg/mL, mouse – BioLegend #100238, human – BioLegend #317326) and soluble anti-CD28 (0.5 μg/mL, mouse – BioLegend #102116, human – BioLegend #302934) for 5 days under the following conditions: Th0 (media alone), Th1 [5 ng/mL IL2 (mouse – BioLegend #575402) and 10 ng/mL IL12 (mouse BioLegend #577004)], and Th22 [30 ng/mL IL6 (mouse – BioLegend #575702 and human – BioLegend #570802), 10 ng/mL IL1β (mouse – BioLegend #575102 and human – BioLegend #579402), 20 ng/mL IL23 (mouse – BioLegend #589002 and human – BioLegend #574102), and 10 μmol/L galunisertib (Tocris #6956)].

    Magnetic Cell Separation:

    Article Title: Aryl hydrocarbon receptor ligands drive pancreatic cancer initiation and progression through pro-tumorigenic T cell polarization
    Article Snippet: Although smoking is a risk factor for pancreatic adenocarcinoma (PDAC), the underlying mechanism promoting tumorigenesis and progression are unknown.. Here, we show that aryl hydrocarbon receptor ligands found in cigarette smoke, like the carcinogen 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), promote pancreatic dysplasia and PDAC progression in a mouse model of this disease.. This effect is mediated by AhR activation in CD4+ T cells, leading to their polarization to interleukin-22 (IL22) producing TH22 cells and to regulatory T cells (Treg) accumulation, ultimately driving a blunted CD8+ T cell effector response.

    Article Title: Aryl Hydrocarbon Receptor Ligands Drive Pancreatic Cancer Initiation and Progression through Protumorigenic T-cell Polarization
    Article Snippet: .. Naïve CD4 + T cells were purified by magnetic cell separation from total splenocytes isolated from murine spleens (Miltenyi Biotec, #130-104-453) or Gift of Life donor spleens (Miltenyi Biotec, #130-094-131) in an isolation buffer [1× PBS, 0.5% BSA, and 2 mmol/L EDTA (Lonza, #51201)]. .. Naïve CD4 + T cells were stimulated in Iscove’s Modified Dulbecco’s Medium (Gibco, #12440-053) supplemented with 10% FBS, 50 μmol/L β-mercaptoethanol (Bio-Rad, #1610710), and 1× penicillin–streptomycin with plate-bound anti-CD3 (2 μg/mL, mouse – BioLegend #100238, human – BioLegend #317326) and soluble anti-CD28 (0.5 μg/mL, mouse – BioLegend #102116, human – BioLegend #302934) for 5 days under the following conditions: Th0 (media alone), Th1 [5 ng/mL IL2 (mouse – BioLegend #575402) and 10 ng/mL IL12 (mouse BioLegend #577004)], and Th22 [30 ng/mL IL6 (mouse – BioLegend #575702 and human – BioLegend #570802), 10 ng/mL IL1β (mouse – BioLegend #575102 and human – BioLegend #579402), 20 ng/mL IL23 (mouse – BioLegend #589002 and human – BioLegend #574102), and 10 μmol/L galunisertib (Tocris #6956)].

    Suspension:

    Article Title: PKM2 diverts glycolytic flux in dependence on mitochondrial one-carbon cycle.
    Article Snippet: .. Briefly, suspension of splenocytes was prepared using gentleMACS Dissociator (Miltenyi). .. Then, B cells isolation (negative sorting) was performed using MojoSort Mouse Pan B Cell Isolation Kit II (Miltenyi), according to manufacturer’s instructions.



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    Image Search Results


    NG-ISACs activate myeloid and lymphoid cells independent of ADCC and ADCP. A, FcγR-mediated activation was assessed using Jurkat-Lucia NFAT-CD16 and NFAT-CD32 reporter cells cocultured with CFPAC-1 tumor cells. ISAC-induced NFAT signaling was measured by Lucia luciferase activity 6 hours after incubation. Glycosylated ISACs are shown with dashed lines whereas NG-ISACs are shown with solid lines. B and C, Mouse BMDM-M2 ( B ) and splenocytes ( C ) were stimulated with E104 for 24 hours, followed by analysis of IL6 production using ELISA. D and E, RAW-Dual reporter macrophages were cocultured with BxPC-3‒TROP2 high ( D ) or CFPAC-1‒TROP2 medium tumor cells ( E ) in the presence of NG-ISACs or controls. Activation of NF-κB signaling pathways was measured. H, Mouse BMDM-M2 cells were cocultured with BxPC-3‒TROP2 high tumor cells and stimulated with NG-ISACs for 24 hours. IL6 production was quantified by ELISA. I, Mouse splenocytes were cocultured with hTROP2-expressing tumor cells and stimulated with NG-ISACs for 24 hours. IL6 production was quantified by ELISA. Data are presented as the mean ± SD ( n = 3), and EC 50 values are from three independent experiments. OD, optical density; RLU, relative light units.

    Journal: Molecular Cancer Therapeutics

    Article Title: Nonglycosylated, Legumain-Cleavable ISACs Drive Potent Antitumor Immunotherapy via a Bystander Effect

    doi: 10.1158/1535-7163.MCT-25-1153

    Figure Lengend Snippet: NG-ISACs activate myeloid and lymphoid cells independent of ADCC and ADCP. A, FcγR-mediated activation was assessed using Jurkat-Lucia NFAT-CD16 and NFAT-CD32 reporter cells cocultured with CFPAC-1 tumor cells. ISAC-induced NFAT signaling was measured by Lucia luciferase activity 6 hours after incubation. Glycosylated ISACs are shown with dashed lines whereas NG-ISACs are shown with solid lines. B and C, Mouse BMDM-M2 ( B ) and splenocytes ( C ) were stimulated with E104 for 24 hours, followed by analysis of IL6 production using ELISA. D and E, RAW-Dual reporter macrophages were cocultured with BxPC-3‒TROP2 high ( D ) or CFPAC-1‒TROP2 medium tumor cells ( E ) in the presence of NG-ISACs or controls. Activation of NF-κB signaling pathways was measured. H, Mouse BMDM-M2 cells were cocultured with BxPC-3‒TROP2 high tumor cells and stimulated with NG-ISACs for 24 hours. IL6 production was quantified by ELISA. I, Mouse splenocytes were cocultured with hTROP2-expressing tumor cells and stimulated with NG-ISACs for 24 hours. IL6 production was quantified by ELISA. Data are presented as the mean ± SD ( n = 3), and EC 50 values are from three independent experiments. OD, optical density; RLU, relative light units.

    Article Snippet: Ramos-Blue reporter cells (2024, InvivoGen, cat. #rms-sp, RRID: CVCL_X591), human peripheral blood mononuclear cells (PBMC; male; iXCells Biotechnologies, November of 2024), mouse BMDM-M2 and splenocytes (March 2024; iQ Biosciences; female, IQB-MSP202), BxPC-3 cells (2023, ATCC, cat. #CRL-1687, RRID: CVCL_0186), RAW-Dual reporter cells (May 2019, InvivoGen, cat. #rawd-ismip, RRID: CVCL_A7ZK), MC38-hTROP2 (April 2024, Kyinno Biotechnology, cat. #KC-1698), Jurkat-Lucia NFAT-CD16 (June 2024, InvivoGen, cat. #jkt-nfat-cd16, RRID: CVCL_A7ZT), and NFAT-CD32 (August 2024, InvivoGen, cat. #jkt-nfat-cd32, RRID: CVCL_A7ZU) were also obtained.

    Techniques: Activation Assay, Luciferase, Activity Assay, Incubation, Enzyme-linked Immunosorbent Assay, Protein-Protein interactions, Expressing