Project:Sex typing with amelogenin/results-20120212: Difference between revisions

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* Chances are we *haven't* ruined our old master mix, which is great (£)
* Chances are we *haven't* ruined our old master mix, which is great (£)
* We should aliquot our master mixes so we don't have to put them through any more thaw / freeze cycles.
* We should aliquot our master mixes so we don't have to put them through any more thaw / freeze cycles.
* We may have too much template (surprisingly, this can be a problem)
* Do we need hot start?


Basically I think we are screwing up the PCR stage: using the wrong temperatures, too-short timings, or whatever. Here is a paper on sex typing with amelogenin:
Basically I think we are screwing up the PCR stage: using the wrong temperatures, too-short timings, or whatever. Here is a paper on sex typing with amelogenin: