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文献和实验Replication timing by density transfer
-Aldrich (previously from Isotec, which is now part of Sigma-Aldrich) "-N" medium =1.61 g yeast nitrogen base w/o amino acids and ammonium sulfate, 11.1 g succinic acid, 6.67 g NaOH per litre. Pronase : We use
Replication timing by density transfer
-Aldrich (previously from Isotec, which is now part of Sigma-Aldrich) "-N" medium =1.61 g yeast nitrogen base w/o amino acids and ammonium sulfate, 11.1 g succinic acid, 6.67 g NaOH per litre. Pronase : We use
Chromosomal DNA Extraction from Gram-positive Bacteria
-HCl (pH 8.0)containing 20 % sucrose (v/v),add lysozyme to 2.5 mg/ml,and incubate at 37℃ for 45 min. 3.Add 9 ml lysis buffer (10 mM Tris-HCl [pH 8.0],1 mM EDTA,500 mg pronase B,1 % SDS),and incubate additional 30 min at 37℃. 4.Phenol and chloroform
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