NH4AcandEtOHprecipitationofDNA

Add NH4Ac (10 M stock or solid) to the sample for a final concentration of 2.5 M, mix (spin at 4℃, transfer the supernatant to a new tube; optional spin for extra purification of the DNA), add 2.5 volumes of EtOH, mix, and spin this time keeping the pellet (watch the liquid as pouring it down the drain to make sure that pellet does not come loose). Turn the tube upside down on a paper towel to allow the EtOH to drain well. Give the pellet a 70 % EtOH rinse (carefully and a little slowly add the EtOH by a DPTP: if the pellet comes loose, spin it again), drain the tube again, and dry the pellet briefly (under the vacuum for 5 to 10 min) before resuspending the DNA in 10:2 TE (almost always TE except doing a digest or ligation in which case the DNA is resuspended in H2O:low salt in the resuspension buffer is important). Often multiple NH4Ac/EtOH precipitation are desired. If the DNA is particularly important or if it is at a very low concentration i.e. <0.5 µg/ml, it is best to include a waiting period before each spin: at least one hour (overnight is better) and at either room temperature or 4 ℃. EtOH and salt reduce the solubility of DNA, consequently, it is best to drain the EtOH well, wiping the inside of the tube with a Chimwipe (but, do not touch the pellet)

Sample Volume of Table

　 　MFT(0.5 ml) 　　　 MFT(1.5 ml) 　　　 Corex 　　　　　　　ORT 250mlDNA 　　105 &mu;l 　210 &mu;l 　　315 &mu;l 　　　　　 2.1 ml 　9 ml 　　　 60.0 mlNH4Ac 　35 &mu;l 　70 &mu;l 　　105 &mu;l 　0.7 ml 　　3 ml 　 12.6 gEtOH 　　350 &mu;l 　700 &mu;l 　　1050 &mu;l 　　　　 　7.0 ml 　30 ml 　　　165.0 ml

Optional spin check:

Min/rpm 　　15/14K 　　　　　　20/14K 　　10/14K 　　　　　　25/9KMin/rpm 　　20/14K 　20/14K 　　20/14K 　　20/14K 　　20/14K 　　25/9K