The qPCR platform from the team behind MIQE, geNorm & qbase+
Every step of the run, guided at the bench.
Add notes as you go — so if something later looks off in analysis, you have the context to decide whether to exclude it.
The run, step by step
Four guided steps at the bench, from collecting material to starting the run. Tap any step to see it in detail.
- 1Collect material
Check off every sample, assay, and reagent the run needs — and note anything off (a freezer running warm, a low tube) right where it happened, before a drop is pipetted.
- 2Prepare mixes
Master-mix volumes calculated per reagent, with overage built in.
No spreadsheet, no arithmetic slips. - 3Fill plate
Step-by-step pipetting guidance for your layout — distribute the mix, add sample and assay, well by well. Flag a slip on the spot ("pipetting error, A9"); the note stays on the well, ready when you analyze.
- 4Start run
Pick the instrument and confirm the cycling protocol.
The run is set up and ready to go.
The qPCR platform from the team behind MIQE, geNorm & qbase+
Every step of the run, guided at the bench.
Add notes as you go — so if something later looks off in analysis, you have the context to decide whether to exclude it.
Collect material
Check off samples, assays, and reagents before you start.Prepare mixes
Fill plate
Follow the pipetting steps, well by well.Start run
Pick the instrument, confirm the protocol.Execution pain / problem section
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Execution deep-dive animation bands
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Execution methodology / FAQ accordion
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From sample list to a run you can trust.
Plate layout, master mixes, and replicate placement, handled for you. Free to start.