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文献和实验Sodium Acetate Precipitation of Small Nucleic Acids
实验步骤 1. Add 2 μl carrier to the nucleic acid solution and mix well. 2. Add 1:10 volume of 3 M sodium acetate and mix thoroughly; for 230 μl of Lower Running Buffer, this will be 23 μl of 3 M
PCR clean up using 3M sodium acetate and chilled absolute ethanol
For each 20 ul of PCR product, prepare the following mixture in 1.5 ml Tube. 2 ul of 3M sodium acetate (NaOAc) pH 4.5 40 ul chilled absolute ethanol. Transfer the PCR product (20ul) into the tube containing
Silver Acetate Autometallography (AMG)
hybridization, in situ PCR and in situ 3SR techniques were born. Silver Acetate AMG was developed and optimized during research visits of Gerhard W. HACKER at the University of Uppsala, Sweden, in joint collaboration with Gorm DANSCHER (Aarhus, DK) and Lars
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