Before running an experiment, prepare your samples and add them to the appropriate wells in the kit input plate according to the loading instructions for the kit. For example, prepare the eight treatment-condition eukaryotic cell culture replicates that have more than 106 cells/mL each and the 8 control-condition replicates of the same cell density.
Steps
- Treat the biological input samples according to the appropriate protocols for the material and the field of study.
- Follow the kit instructions for:
- Cell lysis, nuclease, and other appropriate protein-clearing instructions.
- Determining the protein concentration of cleared cell lysates using established methods such as the Pierce™ BCA Protein Assay Kit (Product No. 23227) or Pierce™ Rapid Gold BCA Protein Assay Kit (Product No. A53226).
NOTE
If the input protein amount is outside the supported range for the kits, the results can be unreliable.
If you created an experiment method file in the Experiment Designer application and want to run these samples in an experiment using the file, see Run an experiment using a method file.
If you want to use these samples in an experiment run without creating an experiment method file, that is, using a default method on the instrument, see Run an experiment using quick start .
CAUTION
Flammable Material
Do not put corrosive material or unauthorized chemicals or reagents into the system. This can cause chemical burns.
CAUTION
Biological Hazard
Do not use biohazardous and infectious materials like pathogen and prion samples. This can cause biological harm.