Team:Chiba/Notebook/Calendar/8 September 2009

(Difference between revisions)

Latest revision as of 18:22, 23 September 2009

We cultured a sample at 37 degrees Celsius.

We transferred cultured sample into plate. We observed samples every 30 min. Here are pictures of samples.

0 nM	1 nM	10 nM	100 nM
1000 nM	All

0 nM	1 nM	10 nM	100 nM
1000 nM

0 nM	1 nM	10 nM	100 nM
1000 nM	All

0 nM	1 nM	10 nM	100 nM
1000 nM	All

0 nM	1 nM	10 nM	100 nM
1000 nM	All

0 nM	1 nM	10 nM	100 nM
1000 nM	All

0 nM	1 nM	10 nM	100 nM
1000 nM	All

0 nM	1 nM	10 nM	100 nM
1000 nM

We did prior culture using glycerol stock(XL10G, plac-LuxI, PSB1, Amp) .

@@ Line 7: / Line 7: @@
 == Measurement of Receiver's Responce by AHL concentration (1)==
-*Inoculation
+=== 13:55 Inoculation===
-:55
 We cultured a sample at 37 degrees Celsius.
-:15
+===16:15 Observation of GFP fluorescence ===
 We transferred cultured sample into plate.
-=== Observation of GFP fluorescence ===
 We observed samples every 30 min.
 Here are pictures of samples.
@@ Line 99: / Line 93: @@
 Image:Chiba_0709_1945_1000_nM.jpg|1000 nM
 </gallery>
 == Check of Sender's AHL generation (1) Day 1 ==