Protocol:- 1.Add 20 μl and mix well
- 2.Incubate at 37°C for 10 minutes.
- 3.Spin down and collect supernatant.
The same step can be surprisingly variable.
How do you know the right way to interpret it, and if it matters for getting high quality data?
- Pipetting
- Inverting Tube
- Flicking
- Washboard
- Vortexing
- Inverting Rack
The same step can be surprisingly variable.
How do you know the right way to interpret it, and if it matters for getting high quality data?
Protocol:Add 20 μl and mix well
- Pipetting
- Inverting Tube
- Flicking
- Washboard
- Vortexing
- Inverting Rack