Hi,
I was trying Butanone Chemotaxis assay with normal N2 worms. I maintained worms at 20 degree in a NGM plate containing HB101. For assay, I used day1 young adult (total animals=100-150). The assay plate is a 90 mm plate with 1.6% agar in 5 mM potassium phosphate pH 6.0, 1 mM Cacl2, 1mM MgSO4. Butanone dilution: 1:1000 (in 95% EtOH). For control spot I use 95% EtOH. Assay time was 2 hrs at 20 degree. However, I am achieving chemotaxis index= 0.4, while in many published articles it is close to 0.8.
Please advice me how can I increase CI?
Thanks in advance.