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文献和实验TRICINE GELS Protocol (For Low MW proteins (
Solution Methanol CP 500ml 50% Acetic Acid CP 100ml 10% H2O 400ml
. Two μL of the desorbed solution were taken and analyzed by gas chromatography. Satisfactory separation was attained by using PEG-20M column. Retention time method was used in the qualitative analysis and peak height method was used in the quantitative
6xHis-tagged protein purification using Qiagen Ni-NTA Column
Buffers:Lysis Buffer (1 liter)50 mM NaH2PO4 6.90g NaH2PO4.H2O (MW 137.99g/mol )300 mM NaCl(up to 2M)17.54gNaCl(MW 58.44)or 60ml 5M10 mM Imidazole (up to 100mM)0.68g (MW 68.08 )10 mM BME (up to 20 mM)0.69 ml stock (14.4M )Adust pH to 8.0 using
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