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ATCC human t lymphocyte jurkat cells
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ATCC human t lymphocyte cell line jurkat
NES-428 modulates pro- and anti-inflammatory cytokine transcription in <t>Jurkat</t> T cells. In the non-treated (NC) group, the cells were simply maintained for 24 h without any stimulation. In the stimulated control (ST) group, the same number of cells was exposed to 50 ng/mL of phorbol 12-myristate 13-acetate (PMA) and 1 µg/mL ionomycin for 6 h. For the NES-428 group, Jurkat cells were first incubated for 24 h with heat-killed NES-428, after which they were stimulated by 50 ng/mL PMA and 1 µg/mL ionomycin for 6 h. Total RNA was extracted from each group, and cytokine expression was analyzed by quantitative real-time PCR. Relative mRNA expression of IL-2, IL-4, IL-6, IL-12, TNF-α and IFN-γ was shown. NC = untreated control; ST = stimulated positive control. Data represent mean ± SD of three independent experiments; p < 0.05 vs. NC.
Human T Lymphocyte Cell Line Jurkat, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/human t lymphocyte cell line jurkat/product/ATCC
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Flow cytometric analysis of Treg purity and CD25 expression. The cytograms show, in the upper line, CD4 vs. dump channel markers (dead cell dye, <t>CD14/CD16/CD19/CD8),</t> and, in the lower line, CD25 vs. FOXP3 expression in gated CD4 T-cells. Right, histogram overlay of CD25 expression in the indicated cell subsets; numbers shown the geometric mean fluorescence intensity.
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ATCC human t lymphocyte cells
Flow cytometric analysis of Treg purity and CD25 expression. The cytograms show, in the upper line, CD4 vs. dump channel markers (dead cell dye, <t>CD14/CD16/CD19/CD8),</t> and, in the lower line, CD25 vs. FOXP3 expression in gated CD4 T-cells. Right, histogram overlay of CD25 expression in the indicated cell subsets; numbers shown the geometric mean fluorescence intensity.
Human T Lymphocyte Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/human t lymphocyte cells/product/ATCC
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NES-428 modulates pro- and anti-inflammatory cytokine transcription in Jurkat T cells. In the non-treated (NC) group, the cells were simply maintained for 24 h without any stimulation. In the stimulated control (ST) group, the same number of cells was exposed to 50 ng/mL of phorbol 12-myristate 13-acetate (PMA) and 1 µg/mL ionomycin for 6 h. For the NES-428 group, Jurkat cells were first incubated for 24 h with heat-killed NES-428, after which they were stimulated by 50 ng/mL PMA and 1 µg/mL ionomycin for 6 h. Total RNA was extracted from each group, and cytokine expression was analyzed by quantitative real-time PCR. Relative mRNA expression of IL-2, IL-4, IL-6, IL-12, TNF-α and IFN-γ was shown. NC = untreated control; ST = stimulated positive control. Data represent mean ± SD of three independent experiments; p < 0.05 vs. NC.

Journal: Nutrients

Article Title: Immunomodulatory Effects of Lactobacillus brevis NES-428 in a Hyperthyroidism Mouse Model: Potential Applications for Graves’ Disease

doi: 10.3390/nu17182967

Figure Lengend Snippet: NES-428 modulates pro- and anti-inflammatory cytokine transcription in Jurkat T cells. In the non-treated (NC) group, the cells were simply maintained for 24 h without any stimulation. In the stimulated control (ST) group, the same number of cells was exposed to 50 ng/mL of phorbol 12-myristate 13-acetate (PMA) and 1 µg/mL ionomycin for 6 h. For the NES-428 group, Jurkat cells were first incubated for 24 h with heat-killed NES-428, after which they were stimulated by 50 ng/mL PMA and 1 µg/mL ionomycin for 6 h. Total RNA was extracted from each group, and cytokine expression was analyzed by quantitative real-time PCR. Relative mRNA expression of IL-2, IL-4, IL-6, IL-12, TNF-α and IFN-γ was shown. NC = untreated control; ST = stimulated positive control. Data represent mean ± SD of three independent experiments; p < 0.05 vs. NC.

Article Snippet: To investigate the immunomodulatory effects of NES-428, the human T lymphocyte cell line Jurkat (ATCC TIB-152) was employed for cytokine expression analysis.

Techniques: Control, Incubation, Expressing, Real-time Polymerase Chain Reaction, Positive Control

Flow cytometric analysis of Treg purity and CD25 expression. The cytograms show, in the upper line, CD4 vs. dump channel markers (dead cell dye, CD14/CD16/CD19/CD8), and, in the lower line, CD25 vs. FOXP3 expression in gated CD4 T-cells. Right, histogram overlay of CD25 expression in the indicated cell subsets; numbers shown the geometric mean fluorescence intensity.

Journal: Journal of Clinical Medicine

Article Title: Validation of a Ready-to-Use Lyophilized Kit for Labeling IL2 with 68 Ga: A New Avenue for Imaging Activated T-lymphocytes in Tumor Microenvironment

doi: 10.3390/jcm14165658

Figure Lengend Snippet: Flow cytometric analysis of Treg purity and CD25 expression. The cytograms show, in the upper line, CD4 vs. dump channel markers (dead cell dye, CD14/CD16/CD19/CD8), and, in the lower line, CD25 vs. FOXP3 expression in gated CD4 T-cells. Right, histogram overlay of CD25 expression in the indicated cell subsets; numbers shown the geometric mean fluorescence intensity.

Article Snippet: - CD8+ T-lymphocytes were isolated using the CD8+ T Cell Isolation Kit, human 130-096-495 for 10 9 total cells (Miltenyi Biotec).

Techniques: Expressing, Fluorescence