I just started learning dual luciferase assay now.( Firefly-Renilla signal)
using HEK 293 cell, and give stimulation by PMA/lono.
the main point is I wonder what if I changes the few conditions, what experiment result make differences? and how?
please let me know what can be changed and the reasons for that.... or how can I get those informations ..
main question is below
4 conditions changed
1. harvest cell include cell debris without centrifuge.
2. less or much amounts of stimulation concentration
3. if I use different concentrations of cell, what is the main differences on data result.
4. do bubbles can distract analysis ?