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  • ホーム
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  • CellCountingSub Section
  • Media Selection for Optimization of Culturing Conditions
Cell Counting and Image Cytometry

Media Selection for Optimization of Culturing Conditions

Section
Cell-based Assays for Bioprocessing
Celigo Applications
Cell Counting Method Selection
Cell Counting and Image Cytometry FAQs
Cell-based Assays for Bioprocessing
Cell-based Assays for Gene Therapy Development
Cellometer Applications
Modern Virology Assays
Sub Section
Bioprocessing Solutions
Bioprocessing Solutions
FDA Regulations of Biologics
Topic
Media Selection for Optimization of Culturing Conditions
Engineering CHO Cells Using CRISPR Technology
High-Throughput Clone Screening Ensures High-Quality Biologic Production
Media Selection for Optimization of Culturing Conditions
Monitoring Growth and Viability
Using Cellaca MX for High-Throughput CHO Cell Counting for Bioprocessing
Single Cell Cloning for Cell Line Development

Media selection

Serum-free cell cultures media has undergone continuous development and optimization efforts with the goal of increasing cell density, viability, and recombinant protein titer [Ritacco et al. 2018]

Fine tuning the media for your specific application can require testing different types and amounts of metabolites, nutrient amino acids, and antioxidants (e.g. DMSO). Considering the need for different concentrations and triplicate samples, media selection can quickly become an overwhelming task that is difficult to track. Image-based cytometry can monitor proliferation and viability to simplify media selection.

img-media-selection-for-optimization-of-culturing-conditions-1.PNG

The example above shows an experiment where three factors were used in different combinations (left panel). CHO cells (10/well) were plated on a 384-well plate (35 replicates per condition). On day 4, proliferation was measured with the Celigo™ image cytometer, and the highest cell counts were observed for samples grown in media containing Factor C (right panel: 1, 5, 6, 7).

Revvity can rapidly and reliably determine the cell concentrations and viabilities in the multiple plates needed to perform these optimization experiments.

  • Perform label-free cell proliferation assays in 96- and 384-well plates at 5 minutes per plate
  • Direct cell counting to determine expression levels from 6- to 1536-well plates
  • High speed, high-throughput, whole-well imaging

High-throughput cell counter provides precise cell counting and viability for 24 samples in <3 minutes.

For research use only. Not for use in diagnostic procedures.

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