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t cell jurkat batch  (Eppendorf AG)


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    Eppendorf AG t cell jurkat batch
    Outputs of capacitance measurements for a <t>T</t> <t>cell</t> <t>(Jurkat)</t> bolus fed process. Panel (A) overlays the online capacitance trace for the LBB process with the viable and total cell concentrations. Feed points have also been marked on the figure. Panel (B) reproduces the lag phase data (the highlighted region in A) for the run to demonstrate the probe's ability to produce correlative results well below the typically observed operational ranges of the probes seen in current biotechnology processes. Panel (C) is a bubble‐plot of viable cell concentration versus capacitance which displays cell diameter and overall culture viability.
    T Cell Jurkat Batch, supplied by Eppendorf AG, used in various techniques. Bioz Stars score: 99/100, based on 191818 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/t+cell+jurkat+batch/pmc13093239-1-0-5?v=Eppendorf+AG
    Average 99 stars, based on 191818 article reviews
    t cell jurkat batch - by Bioz Stars, 2026-07
    99/100 stars

    Images

    1) Product Images from "Capacitance Technology Enables Automated Feeding, Improved Expansion, and Higher Throughput of CAR‐T Cell Stirred‐Tank Bioreactor Cultures"

    Article Title: Capacitance Technology Enables Automated Feeding, Improved Expansion, and Higher Throughput of CAR‐T Cell Stirred‐Tank Bioreactor Cultures

    Journal: Biotechnology Journal

    doi: 10.1002/biot.70226

    Outputs of capacitance measurements for a T cell (Jurkat) bolus fed process. Panel (A) overlays the online capacitance trace for the LBB process with the viable and total cell concentrations. Feed points have also been marked on the figure. Panel (B) reproduces the lag phase data (the highlighted region in A) for the run to demonstrate the probe's ability to produce correlative results well below the typically observed operational ranges of the probes seen in current biotechnology processes. Panel (C) is a bubble‐plot of viable cell concentration versus capacitance which displays cell diameter and overall culture viability.
    Figure Legend Snippet: Outputs of capacitance measurements for a T cell (Jurkat) bolus fed process. Panel (A) overlays the online capacitance trace for the LBB process with the viable and total cell concentrations. Feed points have also been marked on the figure. Panel (B) reproduces the lag phase data (the highlighted region in A) for the run to demonstrate the probe's ability to produce correlative results well below the typically observed operational ranges of the probes seen in current biotechnology processes. Panel (C) is a bubble‐plot of viable cell concentration versus capacitance which displays cell diameter and overall culture viability.

    Techniques Used: Concentration Assay

    Summary data for various feeding regimes employed in T cell (Jurkat) cultures. Panel (A) summarizes the different feeding regimes with respect to process time used for the various Jurkat runs. Panels B‐F all present the graphs of sample time recorded capacitance, viable cell number and culture volume (for ease of understanding feeding implications). Feed zones are marked by the shaded region and relevant detail given in magenta text. Panel (B) = batch process; Panel (C) = LBB; Panel (D) = capacitance‐based bolus; Panel (E) = linear feed; Panel (F) = exponential Feed.
    Figure Legend Snippet: Summary data for various feeding regimes employed in T cell (Jurkat) cultures. Panel (A) summarizes the different feeding regimes with respect to process time used for the various Jurkat runs. Panels B‐F all present the graphs of sample time recorded capacitance, viable cell number and culture volume (for ease of understanding feeding implications). Feed zones are marked by the shaded region and relevant detail given in magenta text. Panel (B) = batch process; Panel (C) = LBB; Panel (D) = capacitance‐based bolus; Panel (E) = linear feed; Panel (F) = exponential Feed.

    Techniques Used:

    Summary data for the different feed regime processes for T cells (Jurkat). Panel (A) gives an overlaid viable cell number graph for the different processes to compare culture time and cell yields obtained across the processes. Panel (B) presents the viability data for the same processes to allow for understanding of where ideal harvest points may occur. Panel (C) contextualizes the harvest point yields (selected as last point of ideal viability) in terms of largest doses of Kymriah for the treatment of either ALL or B‐cell lymphoma.
    Figure Legend Snippet: Summary data for the different feed regime processes for T cells (Jurkat). Panel (A) gives an overlaid viable cell number graph for the different processes to compare culture time and cell yields obtained across the processes. Panel (B) presents the viability data for the same processes to allow for understanding of where ideal harvest points may occur. Panel (C) contextualizes the harvest point yields (selected as last point of ideal viability) in terms of largest doses of Kymriah for the treatment of either ALL or B‐cell lymphoma.

    Techniques Used:



    Similar Products

    t cell jurkat batch  (Eppendorf AG)
    99
    Eppendorf AG t cell jurkat batch
    Outputs of capacitance measurements for a <t>T</t> <t>cell</t> <t>(Jurkat)</t> bolus fed process. Panel (A) overlays the online capacitance trace for the LBB process with the viable and total cell concentrations. Feed points have also been marked on the figure. Panel (B) reproduces the lag phase data (the highlighted region in A) for the run to demonstrate the probe's ability to produce correlative results well below the typically observed operational ranges of the probes seen in current biotechnology processes. Panel (C) is a bubble‐plot of viable cell concentration versus capacitance which displays cell diameter and overall culture viability.
    T Cell Jurkat Batch, supplied by Eppendorf AG, 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/product/t+cell+jurkat+batch/pmc13093239-1-0-5?v=Eppendorf+AG
    Average 99 stars, based on 1 article reviews
    t cell jurkat batch - by Bioz Stars, 2026-07
    99/100 stars
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    Outputs of capacitance measurements for a T cell (Jurkat) bolus fed process. Panel (A) overlays the online capacitance trace for the LBB process with the viable and total cell concentrations. Feed points have also been marked on the figure. Panel (B) reproduces the lag phase data (the highlighted region in A) for the run to demonstrate the probe's ability to produce correlative results well below the typically observed operational ranges of the probes seen in current biotechnology processes. Panel (C) is a bubble‐plot of viable cell concentration versus capacitance which displays cell diameter and overall culture viability.

    Journal: Biotechnology Journal

    Article Title: Capacitance Technology Enables Automated Feeding, Improved Expansion, and Higher Throughput of CAR‐T Cell Stirred‐Tank Bioreactor Cultures

    doi: 10.1002/biot.70226

    Figure Lengend Snippet: Outputs of capacitance measurements for a T cell (Jurkat) bolus fed process. Panel (A) overlays the online capacitance trace for the LBB process with the viable and total cell concentrations. Feed points have also been marked on the figure. Panel (B) reproduces the lag phase data (the highlighted region in A) for the run to demonstrate the probe's ability to produce correlative results well below the typically observed operational ranges of the probes seen in current biotechnology processes. Panel (C) is a bubble‐plot of viable cell concentration versus capacitance which displays cell diameter and overall culture viability.

    Article Snippet: T Cell (Jurkat) batch , Eppendorf 2L glass vessel , Futura , Batch (1.2L).

    Techniques: Concentration Assay

    Summary data for various feeding regimes employed in T cell (Jurkat) cultures. Panel (A) summarizes the different feeding regimes with respect to process time used for the various Jurkat runs. Panels B‐F all present the graphs of sample time recorded capacitance, viable cell number and culture volume (for ease of understanding feeding implications). Feed zones are marked by the shaded region and relevant detail given in magenta text. Panel (B) = batch process; Panel (C) = LBB; Panel (D) = capacitance‐based bolus; Panel (E) = linear feed; Panel (F) = exponential Feed.

    Journal: Biotechnology Journal

    Article Title: Capacitance Technology Enables Automated Feeding, Improved Expansion, and Higher Throughput of CAR‐T Cell Stirred‐Tank Bioreactor Cultures

    doi: 10.1002/biot.70226

    Figure Lengend Snippet: Summary data for various feeding regimes employed in T cell (Jurkat) cultures. Panel (A) summarizes the different feeding regimes with respect to process time used for the various Jurkat runs. Panels B‐F all present the graphs of sample time recorded capacitance, viable cell number and culture volume (for ease of understanding feeding implications). Feed zones are marked by the shaded region and relevant detail given in magenta text. Panel (B) = batch process; Panel (C) = LBB; Panel (D) = capacitance‐based bolus; Panel (E) = linear feed; Panel (F) = exponential Feed.

    Article Snippet: T Cell (Jurkat) batch , Eppendorf 2L glass vessel , Futura , Batch (1.2L).

    Techniques:

    Summary data for the different feed regime processes for T cells (Jurkat). Panel (A) gives an overlaid viable cell number graph for the different processes to compare culture time and cell yields obtained across the processes. Panel (B) presents the viability data for the same processes to allow for understanding of where ideal harvest points may occur. Panel (C) contextualizes the harvest point yields (selected as last point of ideal viability) in terms of largest doses of Kymriah for the treatment of either ALL or B‐cell lymphoma.

    Journal: Biotechnology Journal

    Article Title: Capacitance Technology Enables Automated Feeding, Improved Expansion, and Higher Throughput of CAR‐T Cell Stirred‐Tank Bioreactor Cultures

    doi: 10.1002/biot.70226

    Figure Lengend Snippet: Summary data for the different feed regime processes for T cells (Jurkat). Panel (A) gives an overlaid viable cell number graph for the different processes to compare culture time and cell yields obtained across the processes. Panel (B) presents the viability data for the same processes to allow for understanding of where ideal harvest points may occur. Panel (C) contextualizes the harvest point yields (selected as last point of ideal viability) in terms of largest doses of Kymriah for the treatment of either ALL or B‐cell lymphoma.

    Article Snippet: T Cell (Jurkat) batch , Eppendorf 2L glass vessel , Futura , Batch (1.2L).

    Techniques: