VIABLE COUNT · PLATE ENUMERATION

CFU Calculator: CFU/mL and CFU/g

Calculate colony-forming units from plate counts, dilution fractions, and plated volumes.

CALCULATOR

Enter your plate count

Calculates locally

Example data is prefilled so you can inspect the calculation. Replace it with your measured values.

Plate 1
Countability and replicate plates

Configure countability limits per your regulatory standard or lab protocol. Out-of-range plates are flagged and omitted from pooled averages.

Countable range standard:
YOUR RESULT

Review the default example or enter your plate data to calculate.

How to calculate CFU concentration

A colony-forming unit represents a viable cell or cell cluster capable of forming a visible colony under the selected incubation conditions. Enter the exponent in the dilution (for example, 3 for 10^-3).

Liquid: CFU/mL = colonies ÷ (dilution fraction × plated volume in mL). Solid: CFU/g = colonies × homogenization volume ÷ (sample mass × dilution fraction × plated volume).

Terms and units

Colonies counted (C)
The colonies on the plate. For eligible replicate plates, the calculator pools them as ΣC ÷ Σ(d × V).
Dilution fraction (d)
The portion of the original sample in the tube you plated: a 10⁻³ dilution is 0.001. A factor of 1,000 is the same dilution as its reciprocal fraction.
Plated volume (V)
The volume of that dilution spread or poured onto the plate, in millilitres.
Sample mass (m)
Solid samples only: the mass of the sample in grams, before homogenization.
Homogenization volume (H)
Solid samples only: the volume, in millilitres, that the full sample mass is dispersed into before further dilution.

Worked example

For 86 colonies from a 10⁻³ dilution with 0.1 mL plated, the estimate is 86 ÷ (0.001 × 0.1) = 8.6 × 10⁵ CFU/mL. A zero-colony plate indicates no colonies were detected under those conditions; it does not prove the sample has zero viable organisms.

How to use this calculator

Enter values from your own measurement or validated laboratory method. Review the units and assumptions shown with each result before using it in a report.

Assumptions and limitations

These tools perform arithmetic from the values you provide. They do not validate a laboratory method or replace your laboratory's procedures. Biological samples and instruments can introduce uncertainty that a calculation alone cannot account for.

Frequently asked questions

How do you calculate CFU/mL from a colony count?

CFU/mL = C ÷ (d × V). For 86 colonies from a 10-3 dilution plated at 0.1 mL: 86 ÷ (0.001 × 0.1) = 8.6 × 105 CFU/mL. The CFU/mL calculation guide walks through the same steps.

Which plates should I count?

Most protocols treat about 30–300 colonies as countable; some use 25–250 (for example certain FDA BAM and USP methods) or 10–150 for yeast and moulds. Plates outside the window are flagged as TFTC or TNTC and omitted from pooled averages. Configure the range under "Countability and replicate plates".

What does a plate with zero colonies mean?

It means no colonies were detected under the incubation conditions used. It does not prove the sample contains zero viable organisms — the concentration may simply fall below what the plated volume can detect.

What's the difference between CFU and cells?

One CFU is whatever produced one visible colony: a single cell, or a cluster of cells that stayed together. CFU/mL therefore estimates viable culturable units, not total cell number. See what one CFU represents.

Guides and references