6 (June 6, 2011 GDS)

From 2011.igem.org

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Spin 1.5 mL of overnight culture for 30 secs. in micro-centrifuge. Aspirate off all but 200uL of supernatant and resuspend the pellet by vortexing. Add 300uL of TENS and mix by inversion . The solution should become viscous add 150uL of sodium acetate and vortex. A fine white precipitate should form. Centrifuge for 2.5 minutes. Transfer the supernatant to clean tube and add 2 volumes (1mL) of room temp ETOH. Mix and pellet DNA by centrifugation for 2-5 min. Wash pellet with 70% ethanol and allow pellet to dry. Resuspend the pellet in 30uL TE. Digest 5-10uL as usual.
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P.P. G.E. S.D.
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Latest revision as of 15:11, 24 September 2011