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文献和实验Fastfilter Plasmid Maxi Kit Spin Protocol
high quality DNA. Discard flow-through liquid and reuse the collection tube in the next step. 12. Wash the column by adding 15 ml of DNA Wash Buffer diluted with ethanol. Centrifuge as above and discard flow-through. Note: DNA Wash Buffer
Fastfilter Plasmid Midi Kit Spin Protocol
and centrifuge as above. This step ensures that residual protein contamination is removed and must be included for downstream applications requiring high quality DNA. Discard flow-through liquid and reuse the collection tube in the next step. 12. Wash
E-Z 96® Viral RNA Protocol with Centrifugation
into the each well of the HiBind® RNA plate . Seal the plate with a new sealing film. Centrifuge at 5500 x g for 5 minutes at room temperature. 11. Place HiBind® RNA plate on top of another clean 2ml 96-well plate (Not supplied). Remove the sealing film and add 500 ul Wash
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