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Seeding density, passage dilution, and confluence targets decide whether an experiment starts on the right footing. This category collects calculators for cells per well, subculturing ratios, hemocytometer counts, and growth estimates, alongside the plate setup maths that follows from them. Each calculator states its assumptions about viability and vessel format, so you can match the result to the protocol you are actually running.

Frequently asked questions

  • How do I go from a cell count to seeding a plate?

    Count the suspension with the hemocytometer calculator to get viable cells per mL, then enter that concentration in the cell seeding calculator to get cells per well and the volumes to dispense. If several wells must receive the same number from one uneven suspension, the plate normalization calculator computes the source and diluent volumes per well.

  • Which calculator do I need to plate cells at a defined density?

    For a target density (cells per well or per cm²) use the cell seeding calculator; it converts the viable concentration from your count into suspension and medium volumes per vessel and totals for the whole plate.