succinimidyl ester Thermo Fisher Search Results


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  • 80
    Thermo Fisher alexafluor 488 succinimydyl ester
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    Thermo Fisher carboxyfluorescein diacetate succinimydyl ester cfse
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    Thermo Fisher carboxyfluorescein diacetate succinamidyl ester
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    Thermo Fisher chloromethyfluorescein diacetate succinimidyl ester cfse
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    Thermo Fisher celltrace carboxyfluorescein succinimidyl ester cfse
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    Thermo Fisher succinimidyle ester cfse
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    Thermo Fisher alexa fluor405 a405 succinimidyl ester
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    Thermo Fisher succinimidyl ester cfda
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    Thermo Fisher alexa546 succinimidyl ester
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    Thermo Fisher carboxyfluorescein diacetate succinimidyl ester
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    Thermo Fisher succinimidyl ester cfse stained
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    Thermo Fisher succinimidyl ester cfse labeled
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    Thermo Fisher 6 carboxytetramethylrhodamine succinimidyl ester nhsr
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    Thermo Fisher alexafluor594 succinimidyl esters
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    Thermo Fisher qsy 7 succinimidyl ester
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    Thermo Fisher 5 6 carboxytetramethylrhodamine n succinimidyl ester
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    Thermo Fisher succinimidyl ester kit
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    Thermo Fisher succinimidyl ester cfda se cell tracer kit
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    Thermo Fisher succinymidyl ester
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    Thermo Fisher alexa fluor 647 nhs ester succinimidyl ester
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    Thermo Fisher carboxyfluoroscein succinidyl ester cfse
    Carboxyfluoroscein Succinidyl Ester Cfse, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 70/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher 647 succinimidyl esters
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    Thermo Fisher alexa568 succinimidyl ester
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    Thermo Fisher alexa fluor 488 nhs ester succinimidyl ester
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    Thermo Fisher succinimidyl n maleimidopropionamido tetraethyleneglycol ester
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    Thermo Fisher carboxyfluorescein succinimidyl ester cfse labeling
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    Thermo Fisher carboxyfluorescein diacetate succinamidyl ester cfse
    CD11c + T cells are derivative of T cells and do not possess antigen presenting cell (APC) function. A : transfer of SPN CD45.1 + T cell into RAG2 −/− mice resulted in significant accumulation of CD11c + T cells in SI IEL, while the same population was absent from SI of RAG2 −/− mice. B : 96% of CD11c + T cells in T-cell-transferred RAG2 −/− recipients are CD45.1 positive. C : proliferation of <t>carboxyfluorescein</t> diacetate <t>succinamidyl</t> ester <t>(CFSE)-labeled</t> responder OT-II CD4 + T cells to stimulation by peptide pulsed CD11c + or CD11c − cells from SI and LI. SPN dendritic cells (DC) were used as positive control. DC, SI CD11c + or CD11c − T cells, and LI CD11c + or CD11c − T cells were sorted from C57BL/6 and pulsed with OVA 323–339 peptide added to the coculture with OT-II CD4 + T cells. Ratios of divided CD4 + T cells were calculated to determine response based on reduction of CFSE fluorescence intensity. The data are representative of three individual experiments. WT, wild type.
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    Thermo Fisher 6 carboxyfluorescien diacetate succinimdyl ester
    CD11c + T cells are derivative of T cells and do not possess antigen presenting cell (APC) function. A : transfer of SPN CD45.1 + T cell into RAG2 −/− mice resulted in significant accumulation of CD11c + T cells in SI IEL, while the same population was absent from SI of RAG2 −/− mice. B : 96% of CD11c + T cells in T-cell-transferred RAG2 −/− recipients are CD45.1 positive. C : proliferation of <t>carboxyfluorescein</t> diacetate <t>succinamidyl</t> ester <t>(CFSE)-labeled</t> responder OT-II CD4 + T cells to stimulation by peptide pulsed CD11c + or CD11c − cells from SI and LI. SPN dendritic cells (DC) were used as positive control. DC, SI CD11c + or CD11c − T cells, and LI CD11c + or CD11c − T cells were sorted from C57BL/6 and pulsed with OVA 323–339 peptide added to the coculture with OT-II CD4 + T cells. Ratios of divided CD4 + T cells were calculated to determine response based on reduction of CFSE fluorescence intensity. The data are representative of three individual experiments. WT, wild type.
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    Thermo Fisher alexa 647 succinmidyl ester
    CD11c + T cells are derivative of T cells and do not possess antigen presenting cell (APC) function. A : transfer of SPN CD45.1 + T cell into RAG2 −/− mice resulted in significant accumulation of CD11c + T cells in SI IEL, while the same population was absent from SI of RAG2 −/− mice. B : 96% of CD11c + T cells in T-cell-transferred RAG2 −/− recipients are CD45.1 positive. C : proliferation of <t>carboxyfluorescein</t> diacetate <t>succinamidyl</t> ester <t>(CFSE)-labeled</t> responder OT-II CD4 + T cells to stimulation by peptide pulsed CD11c + or CD11c − cells from SI and LI. SPN dendritic cells (DC) were used as positive control. DC, SI CD11c + or CD11c − T cells, and LI CD11c + or CD11c − T cells were sorted from C57BL/6 and pulsed with OVA 323–339 peptide added to the coculture with OT-II CD4 + T cells. Ratios of divided CD4 + T cells were calculated to determine response based on reduction of CFSE fluorescence intensity. The data are representative of three individual experiments. WT, wild type.
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    Image Search Results


    CD11c + T cells are derivative of T cells and do not possess antigen presenting cell (APC) function. A : transfer of SPN CD45.1 + T cell into RAG2 −/− mice resulted in significant accumulation of CD11c + T cells in SI IEL, while the same population was absent from SI of RAG2 −/− mice. B : 96% of CD11c + T cells in T-cell-transferred RAG2 −/− recipients are CD45.1 positive. C : proliferation of carboxyfluorescein diacetate succinamidyl ester (CFSE)-labeled responder OT-II CD4 + T cells to stimulation by peptide pulsed CD11c + or CD11c − cells from SI and LI. SPN dendritic cells (DC) were used as positive control. DC, SI CD11c + or CD11c − T cells, and LI CD11c + or CD11c − T cells were sorted from C57BL/6 and pulsed with OVA 323–339 peptide added to the coculture with OT-II CD4 + T cells. Ratios of divided CD4 + T cells were calculated to determine response based on reduction of CFSE fluorescence intensity. The data are representative of three individual experiments. WT, wild type.

    Journal: American Journal of Physiology - Gastrointestinal and Liver Physiology

    Article Title: Small intestine CD11c+ CD8+ T cells suppress CD4+ T cell-induced immune colitis

    doi: 10.1152/ajpgi.00032.2010

    Figure Lengend Snippet: CD11c + T cells are derivative of T cells and do not possess antigen presenting cell (APC) function. A : transfer of SPN CD45.1 + T cell into RAG2 −/− mice resulted in significant accumulation of CD11c + T cells in SI IEL, while the same population was absent from SI of RAG2 −/− mice. B : 96% of CD11c + T cells in T-cell-transferred RAG2 −/− recipients are CD45.1 positive. C : proliferation of carboxyfluorescein diacetate succinamidyl ester (CFSE)-labeled responder OT-II CD4 + T cells to stimulation by peptide pulsed CD11c + or CD11c − cells from SI and LI. SPN dendritic cells (DC) were used as positive control. DC, SI CD11c + or CD11c − T cells, and LI CD11c + or CD11c − T cells were sorted from C57BL/6 and pulsed with OVA 323–339 peptide added to the coculture with OT-II CD4 + T cells. Ratios of divided CD4 + T cells were calculated to determine response based on reduction of CFSE fluorescence intensity. The data are representative of three individual experiments. WT, wild type.

    Article Snippet: Purified CD4+ T cells were labeled with 5 μM carboxyfluorescein diacetate succinamidyl ester (CFSE) (Molecular Probes), according to manufacturer's instructions.

    Techniques: Mouse Assay, Labeling, Positive Control, Fluorescence