purified cd8 t cells Search Results


purified rhesus monkey cd8 t cells  (iQ Biosciences)
N/A
High-quality, high-viability (> 90%) CD8 T cells purified from rhesus monkey (or macaque) PBMCs by magnetic selection. Highly enriched (typically > 90%) post-selection purity achieved via magnetic isolation. Used for a wide variety of safety
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human cd8 t cells  (iQ Biosciences)
94
iQ Biosciences human cd8 t cells
Human Cd8 T Cells, supplied by iQ Biosciences, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/purified+cd8+++t+cells/Purified+Human+CD8+T+Cells/pm38326607-499-0-4
Average 94 stars, based on 1 article reviews
human cd8 t cells - by Bioz Stars, 2026-09
94/100 stars
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purified cd8 + t cells from p14 (gp 33–41 ) or tnp4 mice (np 396–404 )  (STEMCELL Technologies Inc)
90
STEMCELL Technologies Inc purified cd8 + t cells from p14 (gp 33–41 ) or tnp4 mice (np 396–404 )
Hepatocyte-activated nucleoprotein-specific CD8 + T cells in uninfected transthyretin-nucleoprotein (TTR-NP) mice do not express proapoptotic Bim protein. ( A ) 2 × 10 6 carboxyfluorescein diacetate succinimidyl ester (CFSE)-labeled naive CD8 + NP 396–404 -specific T cells isolated from TNP4 mice were transferred IV into uninfected TTR-NP and B6 mice. Two days after the adoptive transfer, the proliferation of CFSE-labeled cells was assessed. ( B ) Expression of activation markers CD62L, CD25, and CD69 was assessed on NP 396–404 -specific T cells 2 days after adoptive transfer in TTR-NP or B6 mice. ( C ) Isolated CFSE-labeled NP 396–404 and GP 33–41 -specific CD8 + T cells from TNP4 and <t>P14</t> transgenic mice, respectively, were adoptively transferred into TTR-NP and B6 mice and analyzed for Bim expression by flow cytometry 2 days after transfer. (Representative data of two independent experiments are shown; n = 4 per group.)
Purified Cd8 + T Cells From P14 (Gp 33–41 ) Or Tnp4 Mice (Np 396–404 ), supplied by STEMCELL Technologies Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/purified+cd8+++t+cells/purified+cd8+++t+cells+from+p14++gp+33+41+++or+tnp4+mice++np+396+404++/pmc05301191-57-12-22
Average 90 stars, based on 1 article reviews
purified cd8 + t cells from p14 (gp 33–41 ) or tnp4 mice (np 396–404 ) - by Bioz Stars, 2026-09
90/100 stars
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10 5 magnetic bead-purified peripheral cd8 + t cells from pbmcs  (STEMCELL Technologies Inc)
90
STEMCELL Technologies Inc 10 5 magnetic bead-purified peripheral cd8 + t cells from pbmcs
Hepatocyte-activated nucleoprotein-specific CD8 + T cells in uninfected transthyretin-nucleoprotein (TTR-NP) mice do not express proapoptotic Bim protein. ( A ) 2 × 10 6 carboxyfluorescein diacetate succinimidyl ester (CFSE)-labeled naive CD8 + NP 396–404 -specific T cells isolated from TNP4 mice were transferred IV into uninfected TTR-NP and B6 mice. Two days after the adoptive transfer, the proliferation of CFSE-labeled cells was assessed. ( B ) Expression of activation markers CD62L, CD25, and CD69 was assessed on NP 396–404 -specific T cells 2 days after adoptive transfer in TTR-NP or B6 mice. ( C ) Isolated CFSE-labeled NP 396–404 and GP 33–41 -specific CD8 + T cells from TNP4 and <t>P14</t> transgenic mice, respectively, were adoptively transferred into TTR-NP and B6 mice and analyzed for Bim expression by flow cytometry 2 days after transfer. (Representative data of two independent experiments are shown; n = 4 per group.)
10 5 Magnetic Bead Purified Peripheral Cd8 + T Cells From Pbmcs, supplied by STEMCELL Technologies Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/purified+cd8+++t+cells/10+5+magnetic+bead+purified+peripheral+cd8+++t+cells+from+pbmcs/pmc06037756-164-10-11
Average 90 stars, based on 1 article reviews
10 5 magnetic bead-purified peripheral cd8 + t cells from pbmcs - by Bioz Stars, 2026-09
90/100 stars
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stemcell-purified wt, dgkζ −/− , cbl-b −/− , or dko náive cd8+ t cells  (STEMCELL Technologies Inc)
90
STEMCELL Technologies Inc stemcell-purified wt, dgkζ −/− , cbl-b −/− , or dko náive cd8+ t cells
Hepatocyte-activated nucleoprotein-specific CD8 + T cells in uninfected transthyretin-nucleoprotein (TTR-NP) mice do not express proapoptotic Bim protein. ( A ) 2 × 10 6 carboxyfluorescein diacetate succinimidyl ester (CFSE)-labeled naive CD8 + NP 396–404 -specific T cells isolated from TNP4 mice were transferred IV into uninfected TTR-NP and B6 mice. Two days after the adoptive transfer, the proliferation of CFSE-labeled cells was assessed. ( B ) Expression of activation markers CD62L, CD25, and CD69 was assessed on NP 396–404 -specific T cells 2 days after adoptive transfer in TTR-NP or B6 mice. ( C ) Isolated CFSE-labeled NP 396–404 and GP 33–41 -specific CD8 + T cells from TNP4 and <t>P14</t> transgenic mice, respectively, were adoptively transferred into TTR-NP and B6 mice and analyzed for Bim expression by flow cytometry 2 days after transfer. (Representative data of two independent experiments are shown; n = 4 per group.)
Stemcell Purified Wt, Dgkζ −/− , Cbl B −/− , Or Dko Náive Cd8+ T Cells, supplied by STEMCELL Technologies Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/purified+cd8+++t+cells/stemcell+purified+wt++dgk%CE%B6+++++++cbl+b+++++++or+dko+n%C3%A1ive+cd8++t+cells/pmc06048965-140-50-45
Average 90 stars, based on 1 article reviews
stemcell-purified wt, dgkζ −/− , cbl-b −/− , or dko náive cd8+ t cells - by Bioz Stars, 2026-09
90/100 stars
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cynomolgus pan t cells  (iQ Biosciences)
92
iQ Biosciences cynomolgus pan t cells
Hepatocyte-activated nucleoprotein-specific CD8 + T cells in uninfected transthyretin-nucleoprotein (TTR-NP) mice do not express proapoptotic Bim protein. ( A ) 2 × 10 6 carboxyfluorescein diacetate succinimidyl ester (CFSE)-labeled naive CD8 + NP 396–404 -specific T cells isolated from TNP4 mice were transferred IV into uninfected TTR-NP and B6 mice. Two days after the adoptive transfer, the proliferation of CFSE-labeled cells was assessed. ( B ) Expression of activation markers CD62L, CD25, and CD69 was assessed on NP 396–404 -specific T cells 2 days after adoptive transfer in TTR-NP or B6 mice. ( C ) Isolated CFSE-labeled NP 396–404 and GP 33–41 -specific CD8 + T cells from TNP4 and <t>P14</t> transgenic mice, respectively, were adoptively transferred into TTR-NP and B6 mice and analyzed for Bim expression by flow cytometry 2 days after transfer. (Representative data of two independent experiments are shown; n = 4 per group.)
Cynomolgus Pan T Cells, supplied by iQ Biosciences, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/purified+cd8+++t+cells/Purified+Cynomolgus+Monkey+CD8+T+Cells/10__1158_slash_2326___6066__cir___23___0243-55-0-7
Average 92 stars, based on 1 article reviews
cynomolgus pan t cells - by Bioz Stars, 2026-09
92/100 stars
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Image Search Results


Hepatocyte-activated nucleoprotein-specific CD8 + T cells in uninfected transthyretin-nucleoprotein (TTR-NP) mice do not express proapoptotic Bim protein. ( A ) 2 × 10 6 carboxyfluorescein diacetate succinimidyl ester (CFSE)-labeled naive CD8 + NP 396–404 -specific T cells isolated from TNP4 mice were transferred IV into uninfected TTR-NP and B6 mice. Two days after the adoptive transfer, the proliferation of CFSE-labeled cells was assessed. ( B ) Expression of activation markers CD62L, CD25, and CD69 was assessed on NP 396–404 -specific T cells 2 days after adoptive transfer in TTR-NP or B6 mice. ( C ) Isolated CFSE-labeled NP 396–404 and GP 33–41 -specific CD8 + T cells from TNP4 and P14 transgenic mice, respectively, were adoptively transferred into TTR-NP and B6 mice and analyzed for Bim expression by flow cytometry 2 days after transfer. (Representative data of two independent experiments are shown; n = 4 per group.)

Journal: Cellular and Molecular Gastroenterology and Hepatology

Article Title: Expression of Viral Antigen by the Liver Leads to Chronic Infection Through the Generation of Regulatory T Cells

doi: 10.1016/j.jcmgh.2015.02.002

Figure Lengend Snippet: Hepatocyte-activated nucleoprotein-specific CD8 + T cells in uninfected transthyretin-nucleoprotein (TTR-NP) mice do not express proapoptotic Bim protein. ( A ) 2 × 10 6 carboxyfluorescein diacetate succinimidyl ester (CFSE)-labeled naive CD8 + NP 396–404 -specific T cells isolated from TNP4 mice were transferred IV into uninfected TTR-NP and B6 mice. Two days after the adoptive transfer, the proliferation of CFSE-labeled cells was assessed. ( B ) Expression of activation markers CD62L, CD25, and CD69 was assessed on NP 396–404 -specific T cells 2 days after adoptive transfer in TTR-NP or B6 mice. ( C ) Isolated CFSE-labeled NP 396–404 and GP 33–41 -specific CD8 + T cells from TNP4 and P14 transgenic mice, respectively, were adoptively transferred into TTR-NP and B6 mice and analyzed for Bim expression by flow cytometry 2 days after transfer. (Representative data of two independent experiments are shown; n = 4 per group.)

Article Snippet: We labeled 2 × 10 6 purified CD8 + T cells from P14 (GP 33–41 ) or TNP4 mice (NP 396–404 ) (Stemcell Technologies) with CFSE (5 μM) (Vybrant CFDA SE Cell Tracer Kit; Molecular Probes), and they were adoptively transferred IV into TTR-NP or control B6 mice.

Techniques: Labeling, Isolation, Adoptive Transfer Assay, Expressing, Activation Assay, Transgenic Assay, Flow Cytometry

Hepatocyte-expressed NP is efficiently presented and leads to CD8 + T-cell activation. ( A ) GP 33–41 - and NP 396–404 -specific CD8 + T cells isolated from P14 and TNP4 TCR transgenic mice and labeled with CFSE or efluor450, respectively, were adoptively transferred (1.5 × 10 6 cells) into transthyretin-nucleoprotein (TTR-NP) and B6 mice before low-dose infection with lymphocytic choriomeningitis virus (LCMV)-WE. Proliferation was assessed by flow cytometry 5 days after infection. ( B ) GP 33–41 - and NP 396–404 -specific CD8 + T cells were labeled as described and were adoptively transferred into recombination-activating gene (RAG)-deficient or RAG-deficient TTR-NP mice to monitor the proliferation in absence of infection. Proliferation was assessed 7 days later by flow cytometry. The GP 33–41 (CFSE) and NP 396–404 specific (efluor450) CD8 + T cells before transfer ( dashed lines ) are shown as controls. (Representative data of two independent experiments are shown; n = 4 per group.) ** P < .01.

Journal: Cellular and Molecular Gastroenterology and Hepatology

Article Title: Expression of Viral Antigen by the Liver Leads to Chronic Infection Through the Generation of Regulatory T Cells

doi: 10.1016/j.jcmgh.2015.02.002

Figure Lengend Snippet: Hepatocyte-expressed NP is efficiently presented and leads to CD8 + T-cell activation. ( A ) GP 33–41 - and NP 396–404 -specific CD8 + T cells isolated from P14 and TNP4 TCR transgenic mice and labeled with CFSE or efluor450, respectively, were adoptively transferred (1.5 × 10 6 cells) into transthyretin-nucleoprotein (TTR-NP) and B6 mice before low-dose infection with lymphocytic choriomeningitis virus (LCMV)-WE. Proliferation was assessed by flow cytometry 5 days after infection. ( B ) GP 33–41 - and NP 396–404 -specific CD8 + T cells were labeled as described and were adoptively transferred into recombination-activating gene (RAG)-deficient or RAG-deficient TTR-NP mice to monitor the proliferation in absence of infection. Proliferation was assessed 7 days later by flow cytometry. The GP 33–41 (CFSE) and NP 396–404 specific (efluor450) CD8 + T cells before transfer ( dashed lines ) are shown as controls. (Representative data of two independent experiments are shown; n = 4 per group.) ** P < .01.

Article Snippet: We labeled 2 × 10 6 purified CD8 + T cells from P14 (GP 33–41 ) or TNP4 mice (NP 396–404 ) (Stemcell Technologies) with CFSE (5 μM) (Vybrant CFDA SE Cell Tracer Kit; Molecular Probes), and they were adoptively transferred IV into TTR-NP or control B6 mice.

Techniques: Activation Assay, Isolation, Transgenic Assay, Labeling, Infection, Flow Cytometry