1. Enter the sample or fraction volume
Use the liquid volume being diluted after the centrifuge step, not the original pre-centrifugation volume unless that is truly the aliquot being mixed.
2. Enter added diluent or buffer
Use the same volume unit as the sample input.
3. Enter a diluted concentration if available
This optional numerical input is used to show the concentration corrected by the volume dilution factor.
4. Review the fold dilution
The factor is final mixed volume divided by the sample/fraction volume.
5. Separate dilution from centrifuge recovery
Do not treat this volume ratio as a correction for analyte loss, pelleting efficiency, or residual supernatant unless those effects are independently characterized.