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- 详细信息
- 文献和实验
- 技术资料
- 库存:
10
- 供应商:
北京柏瑞图科技有限公司
- 规格:
96
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文献和实验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
E-Z 96® M13 Isolation Vacuum Manifold Protocol
9. Next, apply the vacuum until all of the liquid passes through the membrane. 10. Add 1 mL of SPW Wash Buffer into each well of the E-Z 96® DNA Plate and switch on the vacuum until all of the liquid has passed through the membran. 11. Remove the E-Z
E.Z.N.A.® Mag-Bind® Viral DNARNA Spin Protocol
containing detergent. DNA/RNA was bound to the surface of Mag-Bind® magnetic particles under proper condition. Proteins and cellular debris are efficiently washed with few wash steps. Pure RNA and DNA is then eluted in nuclease-free water or low ionic
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