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Biology · Lab

Serial Dilution Calculator

Concentration at every tube in a serial dilution.

Final (most dilute) concentration
0.001µg/mL

After 6 serial 10-fold dilutions.

TubeDilutionConcentration (µg/mL)
01:1 (stock)1000
11:10100
21:10010
31:10001
41:100000.1
51:1000000.01
61:10000000.001

In a serial dilution, each tube divides the previous one by a fixed factor, so the concentration of tube n is Cₙ = C₀ ÷ factorⁿ. Starting from 1,000 µg/mL with a 10-fold factor, six steps give 1,000 ÷ 10⁶ = 0.001 µg/mL — a million-fold dilution in six manageable steps.

How a serial dilution works

A serial dilution repeats the same dilution step over and over to span many orders of magnitude — the backbone of standard curves, plate counts, and titrations. Each tube is the previous tube divided by a fixed dilution factor, so the concentration drops geometrically: after n steps it has been divided by the factor n times.

Cₙ = C₀ ÷ factorⁿ

C₀ = stock concentration, n = tube number (0 = stock)

Worked example

Stock of 1,000 µg/mL, a 10-fold dilution factor, six steps:

  1. 1
    Start from the stock (tube 0). C₀ = 1,000 µg/mL, dilution 1:1.
  2. 2
    Apply one 10-fold step. Tube 1 = 1,000 ÷ 10 = 100 µg/mL (1:10).
  3. 3
    Keep dividing by the factor. Tube 2 = 10, tube 3 = 1, tube 4 = 0.1, tube 5 = 0.01 µg/mL.
  4. 4
    Read the final tube. Tube 6 = 1,000 ÷ 10⁶ = 0.001 µg/mL — a million-fold dilution reached in six manageable steps.

Why serial, the bench mechanics, and pitfalls

Why not dilute in one step. Pipetting a 1,000,000-fold dilution directly is wildly inaccurate — you’d transfer a microscopic volume into a huge one. Six 10-fold steps reach the same endpoint with far less error because every transfer is a comfortable volume.

How to hit a given factor. For a 10-fold step, move 1 part sample into 9 parts diluent (factor = (1 + 9) ÷ 1 = 10). For a 2-fold step, mix equal volumes.

Common mistakes. Mix each tube thoroughly before drawing the next transfer, and use a fresh tip every step — carryover on a reused tip inflates the downstream concentrations. Remember tube 0 is the undiluted stock, so n counts the dilution steps, not the tubes.

10-fold series from a 1,000 µg/mL stock

Cₙ = 1,000 ÷ 10ⁿ; matches the tool’s default settings.

Tube (n)DilutionConcentration (µg/mL)
01:1 (stock)1000
11:10100
21:10010
31:10001
41:100000.1
51:1000000.01
61:10000000.001
What does a 10-fold dilution mean?
Each step makes the solution 10× more dilute — for example 1 part sample to 9 parts diluent.
How do I get a specific dilution factor?
Factor = (transfer volume + diluent volume) ÷ transfer volume. For 1 mL into 9 mL, that is 10; for 1 mL into 1 mL, it is 2.
What is tube 0?
The undiluted stock, shown as 1:1 for reference before the first dilution step. The exponent n counts dilution steps, so tube 6 has been diluted six times.
Why use serial dilutions instead of one big dilution?
A single extreme dilution requires pipetting an impractically tiny volume, which is inaccurate. Repeated moderate steps keep each transfer measurable and reduce compounding error.
Do all the steps have to use the same factor?
This tool assumes a constant factor, which is the most common design. A mixed-factor series is possible at the bench but has to be tracked tube by tube.
How do I work back to a concentration I want?
Find the tube whose value matches your target, or pick a factor and step count so that C₀ ÷ factorⁿ lands on it. The table updates as you change the inputs.