Team:Washington/Notebook/Flow Cytometry

From 2009.igem.org

(Difference between revisions)
(→Flow Cytometry)
(→Flow Cytometry)
Line 3: Line 3:
==== Flow Cytometry ====
==== Flow Cytometry ====
-
# Set up overnights of parts 48-51 in terrific broth (TB). Let grow overnight at 37 °C.
+
# Set up overnights of parts J36848-J36851 in terrific broth (TB). Let grow overnight at 37 °C.
# Dilute 20 μL overnight into 1 mL TB and grow at 37 °C until OD 0.3 to OD 0.8.
# Dilute 20 μL overnight into 1 mL TB and grow at 37 °C until OD 0.3 to OD 0.8.
# Add IPTG to 1 mM concentration and let grow for minimum of four hours at room temperature (~23 °C).
# Add IPTG to 1 mM concentration and let grow for minimum of four hours at room temperature (~23 °C).

Revision as of 06:59, 20 October 2009

Uw title logo.png

Flow Cytometry

  1. Set up overnights of parts J36848-J36851 in terrific broth (TB). Let grow overnight at 37 °C.
  2. Dilute 20 μL overnight into 1 mL TB and grow at 37 °C until OD 0.3 to OD 0.8.
  3. Add IPTG to 1 mM concentration and let grow for minimum of four hours at room temperature (~23 °C).
  4. Record OD 600 and add equivalent of 1 μL of OD 2.0 cells to 1mL PBS with 1 mg/mL BSA and specified flourophore concentration (0-100 nM) and allow time to bind (30 minutes to 1 hour).
  5. Preincubate second set of samples in 1 μM biotin to test for nonspecific binding of the fluorophore to the cells
  6. Similarly incubate streptavidin-coated beads with fluorophore in PBS + BSA.
  7. Record cytometry data with 100 μL of each sample.
  8. Centrifuge samples, carefully pipette off supernatant to ~20 μL to avoid disturbing loose pellets, and resuspend samples in 1mL PBS + BSA
    • Spin beads at 1000 x g for 1 minute
      Spin cells at 17,000 x g for 1 minute
  9. Record cytometry data again with reduced fluorescence background


Retrieved from "http://2009.igem.org/Team:Washington/Notebook/Flow_Cytometry"