Difference between revisions of "DsRNA Mediated Knockdown of S2 Cells"

Revision as of 20:00, 29 September 2009

Materials

• S2 Cells. See Culturing S2 Cells
• dsRNA. See Preparation of dsRNA
• S2 Cell Media. See Culturing of S2 Cells

Protocol

• Take a near-confluent plate of S2 cells aspirate media and scrape into 1 mL of fresh media.
• Add 9 mL of fresh media and pipet to mix.
• Using hemocytometer count cells.
  • Add ~100 uL cells under coverslip to hemocytometer.
  • Count one row of 4 squares. For cells touching the edges of the square, only count the top and left line to avoid counting the same cells twice.
  • Record the number of cells (should be 30-150 cells per row) and Calculate cell concentration, where \alpha is number of cells per row

<math>\alpha\times 4 (rows per square) \times 10^5 (dilution factor)</math>