Dear All,

I have a few questions pertaining to the RNA immunoprecipitation procedure.

1. How do we decide if we need to include a cross-linking step in RIP?

2. If a cross-linking step is involved in the RIP procedure, can we prepare a common lysate (that involves cross-linking, quenching and sonication) for ChIP and RIP? Or there is/are any additional step(s) or tricks that we need to take care while preparing the lysate for RIP?

3. Does anyone know of any standard procedure for RIP in the Jurkat cells or any other suspension cells?

Need some valuable inputs.. Thanks

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