jurkat t cells Search Results


90
Shanghai GenePharma jurkat t cell-lines
Jurkat T Cell Lines, supplied by Shanghai GenePharma, 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/jurkat+t+cells/pmc04663632-186-1-16?v=Shanghai+GenePharma
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jurkat t cell-lines - by Bioz Stars, 2026-07
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Federation of European Neuroscience Societies jurkat t cells
Jurkat T Cells, supplied by Federation of European Neuroscience Societies, 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/jurkat+t+cells/pm10413111-25-4-19?v=Federation+of+European+Neuroscience+Societies
Average 90 stars, based on 1 article reviews
jurkat t cells - by Bioz Stars, 2026-07
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Promega blockade bioassay cs186907
Blockade Bioassay Cs186907, supplied by Promega, 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/jurkat+t+cells/us12326450-974-26-1?v=Promega
Average 90 stars, based on 1 article reviews
blockade bioassay cs186907 - by Bioz Stars, 2026-07
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CH Instruments human jurkat t cells lines
Human Jurkat T Cells Lines, supplied by CH Instruments, 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/jurkat+t+cells/pmc06340735-800-3-28?v=CH+Instruments
Average 90 stars, based on 1 article reviews
human jurkat t cells lines - by Bioz Stars, 2026-07
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Kersh Risk Management jurkat t cells
Jurkat T Cells, supplied by Kersh Risk Management, 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/jurkat+t+cells/pm16919488-179-0-38?v=Kersh+Risk+Management
Average 90 stars, based on 1 article reviews
jurkat t cells - by Bioz Stars, 2026-07
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Dr Schulze GmbH jurkat t cells expressing bcl-xl
Jurkat T Cells Expressing Bcl Xl, supplied by Dr Schulze GmbH, 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/jurkat+t+cells/pm15608694-207-10-24?v=Dr+Schulze+GmbH
Average 90 stars, based on 1 article reviews
jurkat t cells expressing bcl-xl - by Bioz Stars, 2026-07
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CEM Corporation jurkat t-cell line dna
Optimization of PCR cycles. <t>DNA</t> samples from 100% <t>Jurkat</t> T-cell line (J, top curve), a mixture of 50% Jurkat and 50% tonsil (0.5 J + 0.5 T, middle curve), 100% tonsil (T, bottom curve), and a negative control including all reagents without DNA (H2O) were amplified for 20 (A), 30 (B), 40 (C), 50 (D), and 60 (E) cycles. B: Jurkat started to produce a sharp −dF/dT peak after 30 PCR cycles. D: The −dF/dT peak height ratio of 100% Jurkat/100% tonsil reached 4.1 at 50 cycles (Table 1). Additional cycles did not significantly improve this ratio. Therefore, the diagnosis of a clonal T-cell gene rearrangement sample was based on DNA melting after 50 PCR cycles. x axis = temperature, ° C; y axis = −dF/dT, where F = fluorescence and T = temperature.
Jurkat T Cell Line Dna, supplied by CEM Corporation, 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/jurkat+t+cells/pmc01867496-145-16-76?v=CEM+Corporation
Average 90 stars, based on 1 article reviews
jurkat t-cell line dna - by Bioz Stars, 2026-07
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Johns Hopkins HealthCare jurkat t cells
Optimization of PCR cycles. <t>DNA</t> samples from 100% <t>Jurkat</t> T-cell line (J, top curve), a mixture of 50% Jurkat and 50% tonsil (0.5 J + 0.5 T, middle curve), 100% tonsil (T, bottom curve), and a negative control including all reagents without DNA (H2O) were amplified for 20 (A), 30 (B), 40 (C), 50 (D), and 60 (E) cycles. B: Jurkat started to produce a sharp −dF/dT peak after 30 PCR cycles. D: The −dF/dT peak height ratio of 100% Jurkat/100% tonsil reached 4.1 at 50 cycles (Table 1). Additional cycles did not significantly improve this ratio. Therefore, the diagnosis of a clonal T-cell gene rearrangement sample was based on DNA melting after 50 PCR cycles. x axis = temperature, ° C; y axis = −dF/dT, where F = fluorescence and T = temperature.
Jurkat T Cells, supplied by Johns Hopkins HealthCare, 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/jurkat+t+cells/pm09875330-6-86-49?v=Johns+Hopkins+HealthCare
Average 90 stars, based on 1 article reviews
jurkat t cells - by Bioz Stars, 2026-07
90/100 stars
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Promega jurkat-ctla4 ja3001
Optimization of PCR cycles. <t>DNA</t> samples from 100% <t>Jurkat</t> T-cell line (J, top curve), a mixture of 50% Jurkat and 50% tonsil (0.5 J + 0.5 T, middle curve), 100% tonsil (T, bottom curve), and a negative control including all reagents without DNA (H2O) were amplified for 20 (A), 30 (B), 40 (C), 50 (D), and 60 (E) cycles. B: Jurkat started to produce a sharp −dF/dT peak after 30 PCR cycles. D: The −dF/dT peak height ratio of 100% Jurkat/100% tonsil reached 4.1 at 50 cycles (Table 1). Additional cycles did not significantly improve this ratio. Therefore, the diagnosis of a clonal T-cell gene rearrangement sample was based on DNA melting after 50 PCR cycles. x axis = temperature, ° C; y axis = −dF/dT, where F = fluorescence and T = temperature.
Jurkat Ctla4 Ja3001, supplied by Promega, 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/jurkat+t+cells/pm39322662-556-0-1?v=Promega
Average 90 stars, based on 1 article reviews
jurkat-ctla4 ja3001 - by Bioz Stars, 2026-07
90/100 stars
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Promega jurkat t cells carrying an nfat-dependent luciferase gene and overexpressing pd-1
Optimization of PCR cycles. <t>DNA</t> samples from 100% <t>Jurkat</t> T-cell line (J, top curve), a mixture of 50% Jurkat and 50% tonsil (0.5 J + 0.5 T, middle curve), 100% tonsil (T, bottom curve), and a negative control including all reagents without DNA (H2O) were amplified for 20 (A), 30 (B), 40 (C), 50 (D), and 60 (E) cycles. B: Jurkat started to produce a sharp −dF/dT peak after 30 PCR cycles. D: The −dF/dT peak height ratio of 100% Jurkat/100% tonsil reached 4.1 at 50 cycles (Table 1). Additional cycles did not significantly improve this ratio. Therefore, the diagnosis of a clonal T-cell gene rearrangement sample was based on DNA melting after 50 PCR cycles. x axis = temperature, ° C; y axis = −dF/dT, where F = fluorescence and T = temperature.
Jurkat T Cells Carrying An Nfat Dependent Luciferase Gene And Overexpressing Pd 1, supplied by Promega, 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/jurkat+t+cells/pmc08401550-148-18-22?v=Promega
Average 90 stars, based on 1 article reviews
jurkat t cells carrying an nfat-dependent luciferase gene and overexpressing pd-1 - by Bioz Stars, 2026-07
90/100 stars
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DiscoverX corporation jurkat t cells
Optimization of PCR cycles. <t>DNA</t> samples from 100% <t>Jurkat</t> T-cell line (J, top curve), a mixture of 50% Jurkat and 50% tonsil (0.5 J + 0.5 T, middle curve), 100% tonsil (T, bottom curve), and a negative control including all reagents without DNA (H2O) were amplified for 20 (A), 30 (B), 40 (C), 50 (D), and 60 (E) cycles. B: Jurkat started to produce a sharp −dF/dT peak after 30 PCR cycles. D: The −dF/dT peak height ratio of 100% Jurkat/100% tonsil reached 4.1 at 50 cycles (Table 1). Additional cycles did not significantly improve this ratio. Therefore, the diagnosis of a clonal T-cell gene rearrangement sample was based on DNA melting after 50 PCR cycles. x axis = temperature, ° C; y axis = −dF/dT, where F = fluorescence and T = temperature.
Jurkat T Cells, supplied by DiscoverX corporation, 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/jurkat+t+cells/us12312405-875-0-16?v=DiscoverX+corporation
Average 90 stars, based on 1 article reviews
jurkat t cells - by Bioz Stars, 2026-07
90/100 stars
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iCell Bioscience Inc human thp-1 t-cell line
Optimization of PCR cycles. <t>DNA</t> samples from 100% <t>Jurkat</t> T-cell line (J, top curve), a mixture of 50% Jurkat and 50% tonsil (0.5 J + 0.5 T, middle curve), 100% tonsil (T, bottom curve), and a negative control including all reagents without DNA (H2O) were amplified for 20 (A), 30 (B), 40 (C), 50 (D), and 60 (E) cycles. B: Jurkat started to produce a sharp −dF/dT peak after 30 PCR cycles. D: The −dF/dT peak height ratio of 100% Jurkat/100% tonsil reached 4.1 at 50 cycles (Table 1). Additional cycles did not significantly improve this ratio. Therefore, the diagnosis of a clonal T-cell gene rearrangement sample was based on DNA melting after 50 PCR cycles. x axis = temperature, ° C; y axis = −dF/dT, where F = fluorescence and T = temperature.
Human Thp 1 T Cell Line, supplied by iCell Bioscience 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/jurkat+t+cells/pm34977002-45-1-10?v=iCell+Bioscience+Inc
Average 90 stars, based on 1 article reviews
human thp-1 t-cell line - by Bioz Stars, 2026-07
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Optimization of PCR cycles. DNA samples from 100% Jurkat T-cell line (J, top curve), a mixture of 50% Jurkat and 50% tonsil (0.5 J + 0.5 T, middle curve), 100% tonsil (T, bottom curve), and a negative control including all reagents without DNA (H2O) were amplified for 20 (A), 30 (B), 40 (C), 50 (D), and 60 (E) cycles. B: Jurkat started to produce a sharp −dF/dT peak after 30 PCR cycles. D: The −dF/dT peak height ratio of 100% Jurkat/100% tonsil reached 4.1 at 50 cycles (Table 1). Additional cycles did not significantly improve this ratio. Therefore, the diagnosis of a clonal T-cell gene rearrangement sample was based on DNA melting after 50 PCR cycles. x axis = temperature, ° C; y axis = −dF/dT, where F = fluorescence and T = temperature.

Journal:

Article Title: Rapid Detection of Clonal T-Cell Receptor-? Gene Rearrangements in T-Cell Lymphomas Using the LightCycler-Polymerase Chain Reaction with DNA Melting Curve Analysis

doi:

Figure Lengend Snippet: Optimization of PCR cycles. DNA samples from 100% Jurkat T-cell line (J, top curve), a mixture of 50% Jurkat and 50% tonsil (0.5 J + 0.5 T, middle curve), 100% tonsil (T, bottom curve), and a negative control including all reagents without DNA (H2O) were amplified for 20 (A), 30 (B), 40 (C), 50 (D), and 60 (E) cycles. B: Jurkat started to produce a sharp −dF/dT peak after 30 PCR cycles. D: The −dF/dT peak height ratio of 100% Jurkat/100% tonsil reached 4.1 at 50 cycles (Table 1). Additional cycles did not significantly improve this ratio. Therefore, the diagnosis of a clonal T-cell gene rearrangement sample was based on DNA melting after 50 PCR cycles. x axis = temperature, ° C; y axis = −dF/dT, where F = fluorescence and T = temperature.

Article Snippet: The polyclonal tonsil background had essentially no influence on the Tm values of the clonally rearranged Jurkat T-cell line DNA when amplified with either primer set A or C (compare lines 1 and 2 in ). table ft1 table-wrap mode="anchored" t5 caption a7 Cell lines Primer set A Primer set C n Tm, mean CV n Tm, mean CV 50% Jurkat 7 86.99 0.45 7 90.18 0.26 100% Jurkat 10 87.25 0.44 5 90.11 0.27 100% CEM 7 91.96 0.32 7 92.14 0.14 Open in a separate window Tm = DNA melting temperature, °C.

Techniques: Negative Control, Amplification, Biomarker Discovery, Fluorescence

Optimization of LightCycler PCR Cycle Number

Journal:

Article Title: Rapid Detection of Clonal T-Cell Receptor-? Gene Rearrangements in T-Cell Lymphomas Using the LightCycler-Polymerase Chain Reaction with DNA Melting Curve Analysis

doi:

Figure Lengend Snippet: Optimization of LightCycler PCR Cycle Number

Article Snippet: The polyclonal tonsil background had essentially no influence on the Tm values of the clonally rearranged Jurkat T-cell line DNA when amplified with either primer set A or C (compare lines 1 and 2 in ). table ft1 table-wrap mode="anchored" t5 caption a7 Cell lines Primer set A Primer set C n Tm, mean CV n Tm, mean CV 50% Jurkat 7 86.99 0.45 7 90.18 0.26 100% Jurkat 10 87.25 0.44 5 90.11 0.27 100% CEM 7 91.96 0.32 7 92.14 0.14 Open in a separate window Tm = DNA melting temperature, °C.

Techniques:

Coefficient of Variation (CV) of LightCycler System Melting Curve Analysis

Journal:

Article Title: Rapid Detection of Clonal T-Cell Receptor-? Gene Rearrangements in T-Cell Lymphomas Using the LightCycler-Polymerase Chain Reaction with DNA Melting Curve Analysis

doi:

Figure Lengend Snippet: Coefficient of Variation (CV) of LightCycler System Melting Curve Analysis

Article Snippet: The polyclonal tonsil background had essentially no influence on the Tm values of the clonally rearranged Jurkat T-cell line DNA when amplified with either primer set A or C (compare lines 1 and 2 in ). table ft1 table-wrap mode="anchored" t5 caption a7 Cell lines Primer set A Primer set C n Tm, mean CV n Tm, mean CV 50% Jurkat 7 86.99 0.45 7 90.18 0.26 100% Jurkat 10 87.25 0.44 5 90.11 0.27 100% CEM 7 91.96 0.32 7 92.14 0.14 Open in a separate window Tm = DNA melting temperature, °C.

Techniques:

Minimal detection of percent clonal T cell. Jurkat T-cell line DNA (100%, 50%, 25%, 12.5%, 6.25%, and 3.125%) was serially diluted into tonsil DNA. After 50 cycles of amplification in the LightCycler system, we could still detect a distinct peak with the expected Tm of Jurkat by DNA melting curve analysis at the 12.5% level with primer set A (A) and at 6.25% level with primer set C (B).

Journal:

Article Title: Rapid Detection of Clonal T-Cell Receptor-? Gene Rearrangements in T-Cell Lymphomas Using the LightCycler-Polymerase Chain Reaction with DNA Melting Curve Analysis

doi:

Figure Lengend Snippet: Minimal detection of percent clonal T cell. Jurkat T-cell line DNA (100%, 50%, 25%, 12.5%, 6.25%, and 3.125%) was serially diluted into tonsil DNA. After 50 cycles of amplification in the LightCycler system, we could still detect a distinct peak with the expected Tm of Jurkat by DNA melting curve analysis at the 12.5% level with primer set A (A) and at 6.25% level with primer set C (B).

Article Snippet: The polyclonal tonsil background had essentially no influence on the Tm values of the clonally rearranged Jurkat T-cell line DNA when amplified with either primer set A or C (compare lines 1 and 2 in ). table ft1 table-wrap mode="anchored" t5 caption a7 Cell lines Primer set A Primer set C n Tm, mean CV n Tm, mean CV 50% Jurkat 7 86.99 0.45 7 90.18 0.26 100% Jurkat 10 87.25 0.44 5 90.11 0.27 100% CEM 7 91.96 0.32 7 92.14 0.14 Open in a separate window Tm = DNA melting temperature, °C.

Techniques: Amplification