Immunology & Binding Assays

Endpoint Titre from Recorded Dilutions

Identify the highest tested dilution meeting an entered replicate rule. Keep bounded, all-negative, all-positive and nonmonotonic outcomes distinct.

Biology · experimental measurements

Summarize an entered dilution-response record without inventing a biological or diagnostic threshold.

Private calculations in your browser · explicit inputs and model boundaries
Example preview · Endpoint bounded by a negativePositive replicate share across dilutions
1:100 · qualifies100 %
1:200 · qualifies100 %
1:400 · qualifies100 %
1:800 · does not qualify0 %

Each bar preserves the observed positive fraction. The entered rule is 100%; dilution steps are shown in ascending order.

  1. 1EnterProvide the known values
  2. 2CalculateResults update automatically
  3. 3VerifyReview the details and units
Try an example

Enter values in %.

One row: reciprocal dilution factor, positive replicates, tested replicates. Enter 100 for a 1:100 dilution. Positivity is determined outside this tool using your method.

Calculation result

Enter valid values to see the result.

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Understand the relationship

The reasoning behind the result

Titre is a reciprocal dilution, not a concentration

The endpoint convention uses the highest dilution that still meets the assay's defined response criterion. A reciprocal value of 400 describes a 1:400 dilution. It does not directly measure antibody mass or concentration.

This tool starts after the assay has classified each replicate. It applies your entered fraction rule to those counts rather than choosing a signal cutoff or interpreting an instrument reading.

The tested range can bound the answer

When the last tested dilution still qualifies, the record establishes only that the endpoint is at least that dilution. When no tested dilution qualifies, the endpoint is below the first tested dilution under the entered rule. Neither case supplies an exact untested value.

A qualifying dilution followed by a nonqualifying dilution gives a recorded endpoint at the last qualifying tested step. The true transition may lie between tested steps; interpolation is not performed.

Preserve irregular patterns

If a nonqualifying dilution is followed by a qualifying one at a higher dilution, the pattern is nonmonotonic. The tool displays the highest observed qualifying step but labels the inconsistency instead of presenting an ordinary endpoint conclusion.

Experimental interference, variability or recording problems require method-specific review. No cause, clinical meaning, treatment implication or significance threshold is inferred from this record.

Follow the numbers

A bounded reciprocal titre of 400

  1. At the 100% replicate rule, 2/2 qualifies and 0/2 does not.
  2. Dilutions 1:100, 1:200 and 1:400 qualify; 1:800 does not.
  3. The highest qualifying tested dilution is 1:400, and the next tested dilution bounds it above.

Report the recorded reciprocal titre as 400 with its tested dilution series and rule; no concentration or clinical interpretation follows.

Quick guide

How to use this calculator

  1. Enter the positivity rule for replicates from the actual method.
  2. Enter recorded positive and tested counts at each dilution.
  3. Read the highest qualifying dilution together with its bound and monotonicity status.
  4. Retain the original record; this calculation does not diagnose a condition or compare assay methods.

Calculation method

Calculation and interpretation

Summarize an entered dilution-response record without inventing a biological or diagnostic threshold.

Qualifiesᵢ = positiveᵢ/testedᵢ ≥ entered rule; recorded titre = greatest qualifying reciprocal dilution

Worked example

A bounded reciprocal titre of 400

Report the recorded reciprocal titre as 400 with its tested dilution series and rule; no concentration or clinical interpretation follows.

Qualifiesᵢ = positiveᵢ/testedᵢ ≥ entered rule; recorded titre = greatest qualifying reciprocal dilution

Supported inputs

Precision and limits

An entered laboratory plan

This tool reconciles the measurements and choices you enter. It does not select a biological protocol, certify a preparation, assess sample suitability or establish an equipment operating limit.

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