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- 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:✕This summary was generated using AI based on multiple online sources. To view the original source information, use the "Learn more" links.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 sampleswww.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… - bing.com › videosWatch full video
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