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Ni-NTA Spin Kit (50)
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文献和实验6xHis-tagged protein purification using Qiagen Ni-NTA Column
)Centrifuge lysate at 10,000xg for 20’ at 40℃to pellet the cellular debris and save supernatant.Add 5μl 2xSB to 5μl Supernatant and store at 200℃for SDS-PAGE analysisBatch purification under Native ConditionsAdd 2.5 ml of the 50% Ni-NTA slurry to 10 ml cleared
Fastfilter Plasmid Maxi Kit Spin Protocol
Column into a 50 ml collection tube, provided. Add 5 ml of Buffer GPS to the column and Lit it sit at room temperature for 3-10 min. Spin in a swinging bucket rotor at 3,000-5,000 x g for 5 minutes at room temperature. Discard the eluate and assemble
Fastfilter Plasmid Midi Kit Spin Protocol
实验步骤 Growth of bacterial culture: 1. Culture volume: Inoculate 30-50 ml LB/ampicillin (50 ug/ml) medium placed in a 200-400 milliliter culture flask with E.coli carrying desired plasmid and grow at 37°C
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