Team:Tokyo Tech/Projects/Lux-Tet hybrid promoter/index.htm

From 2012.igem.org

Revision as of 06:33, 4 September 2012 by Takuo (Talk | contribs)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)

bar

Tokyotechlogo2012.png

LasR generator

Abstract

We succeeded in constructing and characterizing a NEW Biobrick device (name). This device is a LasR generator We found that the device is (explain)

Introduction

TEXT

Rusult

Text

Conclusion

Text

Discussion

Text

Material&Method

Construction

Samples

Strain

Protocol

1.Prepare overnight culture at 37 degrees for 12hours. (2 tubes for each sample)

2.Take 30 μl of the overnight culture of reporter cell into LB + antibiotics (Amp + Kan). (→fresh culture)

3.Incubate the flesh culture of reporter cell] until the observed O.D. reaches around 0.60. and gather the supernatant of culture of inducer cell.

4.Each sample of reporter cell was divided into 2. Prepare and add AHL mixture to one, cell-synthesized AHL to another one, and DMSO mixture to the other.

5.Induction of reporter cell for 3 hours.

6.Fluorometer (FLA5200) and flow cytometry measurements for GFP expression of reporter cell