At this meeting we electrophoresis. Adriana first showed us how to prepare plates and prepared the gel. To use a gel buffer (tristaurinaEDTA) piperazine acrylamide, ethylene glycol, formamide, distilled water, persulfate and fear.
The pipette we use for acrylamide should be dismissed because the chemical (uncured) is very toxic.
We had to do twice the gel because it gelled.
When the race was ready we took her to UV. Adriana
showed us copies of gels and some gels that were saved and we get information to photocopy.
today Photos: http://www.slide.com/r/dK0Ktq5E6z-ZwTjUdp-hN3zVFdFyHwiq?previous_view=mscd_embedded_url&view=original
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