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Project:Blood typing: Difference between revisions

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* Increased PCR cycles from 35 to 40, and increased amount of product loaded onto gel. These could explain results being better than normal.
* Increased PCR cycles from 35 to 40, and increased amount of product loaded onto gel. These could explain results being better than normal.
* First pipetting of Will gDNA went over gel instead of into hole. We repeated but could explain diffusion + weak band.
* Odd that PC gDNA travelled further in gel than our extractions.
* Odd that PC gDNA travelled further in gel than our extractions
* Also more confirmation that there's seemingly no correlation between strength of gDNA and strength of PCR product.
* Also more confirmation that there's seemingly no correlation between strength of gDNA and strength of PCR product.
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