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- 9000347-1 mg
- 2026年04月15日
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文献和实验E.Z.N.Z.TM MicroElute RNA Clean-up Protocol
实验步骤 1. Measure the volume of sample and adjust the sample volume to 100ul with DEPC-Water and proceed to step 2. 2. Add 350ul QVL Lysis buffer and mix by vortexing at maximum speed for 15 seconds. When process small
E.Z.N.Z.TM MicroElute RNA Desalting and Concentration protocol
(supplied with kit), centrifuge at 10,000 x g for 30 seconds at room temperature. Discard flowthrough and re-use the collection tube. 5. Place column in the same 2 ml collection tube from step 4 and add 500 ul RWB Wash Buffer diluted with absolute
E.Z.N.A.® Protocol for Bacteria
flow-through. Then empty the collection tube and centrifuge the spin cartridge for 10 min at 4000-5000 x g to completely dry the HiBind™ matrix. 8. RNA Elution. Transfer column to a clean 15 ml collection tube (Not supplied) and elute RNA with 250
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