Jeff:LabNotes/Midas Animation: Difference between revisions
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>Dinh mNo edit summary |
>Dinh mNo edit summary |
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* I agree with Matt about the weird pronunciation for polymerase. | * I agree with Matt about the weird pronunciation for polymerase. | ||
* Does not mention how the fluorescence get incorporated with new DNA. | * Does not mention how the fluorescence get incorporated with new DNA. | ||
* | * Primer binding pattern seems non-random, although the primer sequences are different, should it be evenly spaced? |
Revision as of 00:02, 23 August 2013
Matt's comments:
Really cool video and easy to understand! and all my comments here are just trying to be nit-picky
- At 00:45 should the DNA be fragmented? If so, should the voice mention that?
- Starting at 1:00 every time it says polymerase it sounds like "pall-mer-aze"
- At 1:30 for the MDA, shouldn't the polymerases keep going and not get stuck?
- At 2:24, why are the first 2 PCR tubes next to each other and all the others are organized every-other. It makes the first corner tube seem unique
Dinh's comments:
- Very cool how the color of the solution changes to indicate new mixtures.
- I agree with Matt about the weird pronunciation for polymerase.
- Does not mention how the fluorescence get incorporated with new DNA.
- Primer binding pattern seems non-random, although the primer sequences are different, should it be evenly spaced?