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- 2025年07月15日
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文献和实验E.Z.N.A.® Mag-Bind® Viral DNARNA Spin Protocol
, or centrifuge at 4000 x g for 10 min for 96-well plate. Remove and discard the supernatant. 9. Repeat step 7-8 by adding another 0.7 ml SPR Wash Buffer to each sample. 10. Remove and discard the supernatant. Briefly spin to collect the liquid
E.Z.N.A.® Mag-Bind® Viral DNA/RNA Spin Protocol
实验原理 If using the E.Z.N.A.™ Mag-Bind® Viral DNA/RNA Kit for the first time, please read this booklet to become familiar with the procedure and its various modification. Samples are lysed in a specially formulated buffer
E.Z.N.A.® Viral RNA Spin Protocol
of absolute ethanol (room temperature, 96-100%) to the sample, mix throughly by vortexing at maxi speed for 30 seconds. 5. Apply the 650 ul of the mixture (including any precipitate) to a HiBind® RNA column assembled in a 2 ml collection tube (supplied
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