Hi all,

I am wondering if everyone gets a stable expression hence readout of Renilla Luciferase among different samples, which is used as an internal control for the normalisation of Firefly readout in a dual luciferase (DLR) assay system. I am performing DLR experiments using the DLR kit from Promega and I achieve varying Renilla readout. I did quite a lot of troubleshooting but nothing really ameliorated. I appreciate if you may share your experiences. Thanks in advance!

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