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→Workshop 2 (Gel electroforese chamber)
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*5. cutting out endings of agarose for screws (screws get hot when letting electricity through and therefore it needs liquid outside) | *5. cutting out endings of agarose for screws (screws get hot when letting electricity through and therefore it needs liquid outside) | ||
*6. pouring the liquid (distiled water + the solution; no agarose) | *6. pouring the liquid (distiled water + the solution; no agarose) | ||
*7. pipetting dna ladder for measurements into the first gel pocket | *7. pipetting dna ladder for measurements into the first gel pocket. https://www.addgene.org/plasmid-protocols/gel-electrophoresis/ | ||
*8. pipetting samples with colouring (instead of colour one could use 40% glicerol so the samples sink into the gel pockets) into the remaining gel pockets | *8. pipetting samples with colouring (instead of colour one could use 40% glicerol so the samples sink into the gel pockets) into the remaining gel pockets | ||
*9. waiting 40 min | *9. waiting 40 min | ||