Abstract: The inputs include separate E. coli glycerol stocks for each of 3 variants, distributed according to the provided function plate map (see attachments). The protocol begins with several growths which convert the separate glycerol stocks into cultures that have reached stationary phase in a 96-well plate. The glycerol stocks are first grown overnight in separate tubes. The next morning, the optical density (OD) of each culture is measured, and then each culture is distributed into a 96-well growth plate. This plate is placed in a plate reader/incubator to grow to stationary phase (~12 hours) without antibiotics or additives (except those required for plasmid maintenance). After this point, the cultures are ready to act as an inputs for the next growth cycles where a 2-fold dilution series of the corresponding inducer is introduced. Throughout the subsequent growths, optical density (OD) and fluorescent measurements are recommended to be taken every 5 minutes and at the end of each growth plate's incubation. The growth cycles are all ~3 hours long, so that cells stay in mid-log phase. At the end of the last growth cycle, the cultures in the growth plate act as input for quantifi cation using either a flow-cytometry or a plate reader.
Keywords:
Deep mutational scanning ; protein sequence-function relationships ; fitness landscape ; laboratory automation ; flow cytometry
Chemistry
Pharmaceutical Intermediates
Inhibitors/Agonists
Material Science
For Research Only
120K+ Compounds
Competitive Price
1-2 Day Shipping
