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联硕生物
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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
Assembly of Nucleosomal Templates by Salt Dialysis
recipeLow‐salt Buffer (see recipe ) recipeZero‐salt buffer (see recipe ) 10% and 30% glycerol gradient buffer
Sections 5-10, micron unfixed, or cold formol calcium/gum sucrose fixed Cryostat sections. Stock solutions A) Pararosanilin-HCL Stock Pararosanilin 1g Distilled water 20ml HCl Conc 5ml
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