- ￥390
- 钦诚生物
- 上海
- QC25-03767
- 2025年07月08日
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- 详细信息
- 文献和实验
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- 保存条件：
室温
- 保质期：
一年
- 供应商：
钦诚生物
- 规格：
250ML
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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)
and the detection of metallic gold and silver, and sulfides and selenides of mercury, silver and zinc. Solutions A and B should be freshly prepared for every run. Solution A: Dissolve 80 mg silver acetate (code 85140; Fluka, Buchs, Switzerland) in 40 mL
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