Dilution Formula:
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Cell culture dilution is the process of adjusting the concentration of cells in a culture medium to achieve a desired cell density for experiments or subculturing. Proper dilution is essential for maintaining healthy cell growth and consistent experimental conditions.
The calculator uses the dilution formula:
Where:
Explanation: The formula calculates the total volume needed to dilute an initial cell suspension to achieve the desired concentration.
Details: Accurate cell dilution is crucial for maintaining consistent cell densities in experiments, preventing overcrowding, and ensuring proper nutrient availability for cell growth.
Tips: Enter the initial volume in mL, initial cell concentration in cells/mL, and desired final concentration in cells/mL. All values must be positive numbers.
Q1: How do I count cells for accurate dilution?
A: Use a hemocytometer or automated cell counter after trypan blue staining to determine viable cell concentration.
Q2: What's the typical cell concentration for subculturing?
A: This varies by cell type, but common ranges are 1-5×10⁴ cells/mL for adherent cells and 2-5×10⁵ cells/mL for suspension cultures.
Q3: Should I account for cell doubling time?
A: For long-term cultures, yes. The calculated dilution provides the starting concentration; cells will continue to multiply.
Q4: How does this differ from serial dilution?
A: This calculates a single-step dilution. Serial dilution involves multiple sequential dilution steps for greater dilution factors.
Q5: What medium should I use for dilution?
A: Use the same culture medium that the cells are growing in, pre-warmed to appropriate temperature with required supplements.