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实验方法

实验方法

RNASafer® Protocol for Total RNA Isolation

来源：互联网关键词： rnasafer protocol isolation

实验步骤

1. Protocol for total RNA purification from tissue sample with E.Z.N.A.^® Total RNA System

1) Remove sample from RNASafer^® Reagent using forceps.

2) Estimate the amount of the tissue and select appropriate E.Z.N.A.^® Total RNA Kit. Use RNA Miniprep Kit (R6634) for less than 40mg tissue, Total RNA Midiprep kit (R6664) for 200mg tissue, RNA Maxiprep Kit(R6693) for 1 gram tissue.

3) For RNA isolation using RNA miniprep kit, add 700ul TRK lysis buffer. Homogenize the tissue with a rotor-stator homogenizer. For RNA isolation using Midi and Maxiprep kit, follow the standard protocol in the user manual.

4) Follow standard protocol for E.Z.N.A.^® Total RNA Kits in user manuals.

2. Protocol for total RNA purification from culture cells and white blood cells with E.Z.N.A.^® Total RNA System

1) For RNA isolation using RNA miniprep kit, take 150ul cell/RNASafer^® Reagent mixture to a RNase free 1.5 ml tube. Add 200ul TRK lysis buffer and mix with 350ul 70% ethanol. For RNA isolation using Midi and Maxiprep kit, follow the standard protocol in the user manual.

2) Apply the sample to the HiBind^® RNA column and follow standard protocol in user manual for each kits.

注意事项

When working with RNASafer^® Reagent use gloves and eye protection (safety goggles) and avoid contact with skin or clothing. Unless otherwise noted, all steps are to be carried out at room temperature (20°C -25°C).

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