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  2. Here is a protocol for the PicoGreen assay12:
    • Protect PicoGreen from light.
    • Dilute PicoGreen 1:200 in 1x TE buffer.
    • Add 100 μl of the PicoGreen working solution into each well of a white 96-well plate.
    • Pipette 100 μl of blank, DNA standard dilutions and samples into the wells of the plate with a defined number of replicates.
    • Swirl the bottle to mix the PicoGreen.
    • An additional 1 ml TE with 5 ul PicoGreen may need to be prepared for the standards.
    • Add PicoGreen to DNA samples.
    Learn more:
    PicoGreen Should be protected from light. 100 ul of diluted PicoGreen is needed per sample/standard. For each DNA plate to be quantified add: 10 ml 1x TE 50 ul PicoGreen Mix by swirling bottle. (An additional 1 ml TE with 5 ul PicoGreen may need to be prepared for the standards.) Add PicoGreen to DNA samples
    www.k-state.edu/igenomics/equipment/documents/…
    Procedure for 96-well plate assay Pipette 100 μl of blank, DNA standard dilutions and samples into the wells of white 96-well plate with a defined number of replicates (having at least 2- 3 replicates is recommended). Add 100 μl of the PicoGreen working solution into each well.
    assets.thermofisher.com/TFS-Assets/LCD/Applicati…
     
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