"
Team:Newcastle/10 September 2010
From 2010.igem.org
(Difference between revisions)
Shethharsh08 (Talk | contribs) (→Result and Conclusion) |
Shethharsh08 (Talk | contribs) (→Result and Conclusion) |
||
| Line 18: | Line 18: | ||
==Result and Conclusion== | ==Result and Conclusion== | ||
| - | Please refer to: [[Team:Newcastle/Filamentous_Cells#Characterisation|Characterisation]] for the result | + | Please refer to: [[Team:Newcastle/Filamentous_Cells#Characterisation|Characterisation]] for the result. |
| - | + | ||
{{Team:Newcastle/footer}} | {{Team:Newcastle/footer}} | ||
Latest revision as of 03:14, 26 October 2010
| |||||||||||||
| |||||||||||||
Contents |
Characterization of yneA
Aim
The aim of this experiment is to prepare slides for the Bacillus subtilis 168 cells which have yneA on the plasmid (pMutin4 and pMap65) and under lacI regulation and are induced by IPTG at various concentrations.
Materials and Protocol
Please refer to: Slide preparation for IPTG induced cells for materials and protocol. For this experiment we used the following cell colonies:
- Bacillus subtilis 168
- Bacillus subtilis 168 with pMutin4 having yneA insert
- Bacillus subtilis 168 tith pMap65 having yneA insert
Today we see the cells on a flourescent microscope.
Result and Conclusion
Please refer to: Characterisation for the result.
   
|
    
|
