E.Z.N.Z.TMMicroEluteRNACleanupProtocol

實驗概要

This protocol is designed to recovery RNA from enzymatic reactions such as DNase I digestion, In vitro transcription, etc. For RNA desalting or clean-up from sample using RNA-Solv Reagent or other phenol involved reagents, please use RNA desalting protocol.

實驗步驟

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 amount of RNA (?2 ug). Add 2 ul of Linear Acrylamide to the mixture.

Note: Remember to add 20 ul of 2-mercaptoethanol per 1 ml of QVL Lysis Buffer before use.

3. Add 250ul absolute ethanol (96-100%, room temperature) to the sample and mix thoroughly by vortexing.

4. Apply sample from step 3 to HiBind^? MicroElute RNA column inserted in a 2 ml collection tube (supplied). The maximum capacity of the spin cartridge is 700 ul. (Larger volumes can be loaded successively.) A precipitate may form upon addition of ethanol in Step 3. Vortex and add the entire mixture to the column. With the spin column inside a 2ml collection tube (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 ethanol. Centrifuge and discard flowthrough.

Note: RWB Wash Buffer Concentrate must be diluted with absolute ethanol before use. Refer to label on bottle for directions.

6. Place column back into the same collection tube from step 5, and add another 500 ul RWB Wash Buffer diluted with absolute ethanol. Centrifuge and discard the flow-through and collection tube.

7. Place the column into a new 2 ml collection tube (supplied). Centrifuge the column at full speed ($13,000 x g) for 2 minutes. Discard the flow-through and the collection tube.

8. Elution of RNA. Transfer the column to a clean 1.5 ml microfuge tube (not supplied with kit) and pipet 15-30 ul of DEPC-treated water (supplied with kit) into the column. Make sure to add water directly onto center of column matrix. Incubate at room temperature for 2 min. Centrifuge for 1 min at maximum speed. A second elution may be necessary if the expected yield of RNA >20 ug.

Alternatively, RNA may be eluted with a smaller volume of water. While reduced elution volume reduce the RNA yield, the concentration will be higher since more than 80% of RNA is recovered with the first elution. Pre-heating the water to 65°C before adding to column and incubating column 2 min at room temperature before centrifugation may increase yields. Elution with less than 10ul volume is not recommended.