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Tuesday: We did a mini-prep of our religated part containing our Gene (BBa_E1010) & double terminator (BBa_B0015). We did this to isolate our plasmid from the bacteria.

Thursday: We digested our sample and ran a gel to confirm if our second attempt at religating the Gene (BBa_E1010) & double terminator (BBa_B0015) Was successful or not; around 800bp

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