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Image Search Results
Journal: Endocrinology
Article Title: The Thyroid Hormone Inactivating Type 3 Deiodinase Is Essential for Optimal Neutrophil Function: Observations From Three Species
doi: 10.1210/en.2017-00666
Figure Lengend Snippet: Flow Cytometry Antibodies
Article Snippet: Manufacturer Ly-6G PerCP-Cy5.5 Rat IgG2A; monoclonal 1A8 560602 BD Biosciences Ly-6C PE Rat IgG2c; monoclonal HK1.4 12-5932 eBioscience CD117 (cKit) APC Rat IgG2b; monoclonal 2B8 17-1171 eBioscience CD11b APC-Cy7 Rat IgG2b;
Techniques: Flow Cytometry, Blocking Assay
Journal: Endocrinology
Article Title: The Thyroid Hormone Inactivating Type 3 Deiodinase Is Essential for Optimal Neutrophil Function: Observations From Three Species
doi: 10.1210/en.2017-00666
Figure Lengend Snippet: Antibody Table
Article Snippet: Manufacturer Ly-6G PerCP-Cy5.5 Rat IgG2A; monoclonal 1A8 560602 BD Biosciences Ly-6C PE Rat IgG2c; monoclonal HK1.4 12-5932 eBioscience CD117 (cKit) APC Rat IgG2b; monoclonal 2B8 17-1171 eBioscience CD11b APC-Cy7 Rat IgG2b;
Techniques: Sequencing, Blocking Assay
Journal: Scientific Reports
Article Title: Deciphering the role of protein kinase A in the control of FoxP3 expression in regulatory T cells in health and autoimmunity
doi: 10.1038/s41598-024-68098-z
Figure Lengend Snippet: PKA inhibition affects the immunometabolic asset and phenotype of Tconv cells during their diffentiation towards iTreg cells and their suppressive function ( a ) Left, kinetic profile of ECAR in human mPKAI-Tconv and CTR-Tconv cells TCR-stimulated or not for 12 h. ECAR was measured in real time, under basal conditions and in response to glucose, oligomycin, and 2-DG. Data are shown from three independent experiments at least in technical duplicates (n = 10). Right, parameters of the glycolytic pathway were calculated from the ECAR profile of Tconv cells in the above-mentioned conditions. Data are expressed as mean ± SEM of three different measurements, each of them in ten replicates (n = 30). ( b ) Representative dot plots (left) and cumulative data (right) of CD25, FoxP3-All and FoxP3-E2 in mPKAI-Tconv and CTR-Tconv cells. Data are shown from eleven independent experiments (n = 11). ( c ) Scatter plots showing the expression of CTLA-4, PD-1 and GITR gated on CD4 + FoxP3-All + (top) or CD4 + FoxP3-E2 + (bottom) in mPKAI-Tconv and CTR-Tconv cells. Data are shown as mean ± SEM from four independent experiments in duplicates (n = 8). ( d ) Left, flow cytometry histograms showing proliferation of CFSE + CD4 + T cells TCR-stimulated for 96 h in vitro and cultured alone (empty curves) or in the presence of various numbers of flow-sorted iTreg from mPKAI-Tconv and CTR-Tconv cells. Numbers in plots indicate the percent of CSFE dilution in CD4 + T cells cultured alone (top left) and co-cultured with iTreg cells (above bracketed lines), as indicated. Right, cumulative data of CD4 + T cell proliferation in the above conditions. Data are shown from four independent experiments in duplicates (n = 8). Independet experiments refer to different individuals.
Article Snippet: For the simultaneous evaluation of surface and intracellular molecules, human iTreg cells were stained with the following antibodies: FITC anti-CD4 (Clone RPA-T4, Cat: 561842) (BD Pharmingen),
Techniques: Inhibition, Expressing, Flow Cytometry, In Vitro, Cell Culture