$$\rightleftharpoonup{xx}$$
$$\longleftharp{xx}$$,
$$\longrightharp{xx}$$,
1. Adaptation for Screening Multiple Caenorhabditis elegans Strains or Knockdowns (Ribonucleic Acid Interference (RNAi) Screen Setup)
Note: This is an RNAi screen described for a 24-well plate setup.
- Add 1 mL of S Basal per well of a 24-well plate containing worms seeded with RNAi. Gently agitate worms by shaking the plate, then transfer worms to an empty, sterile 24 deep-well plate. Allow worms to settle gravitationally (~5 minutes).
- Aspirate supernatant, leaving approximately 1 mL. Add 7 mL of S Basal to each well.
- Repeat steps 1.1 - 1.2 a minimum of 2 more times. After final wash, aspirate supernatant, leaving approximately 400 µL.
- Using the Resampler function of the worm sorter, sort 22 worms from the 24-well plate worm suspension into each well of a 384-well plate (each well of a 24-well plate yields 8 - 12 wells of a 384-well plate).
- To avoid starvation, pipette bacteria into 384-well plates (either a strain that serves solely as food, such as OP50, or a pathogenic strain) prior to sorting.
- After worms have been sorted into the 384-well plate, add small molecules or other experiment-specific materials.