User:Behzad Damadzadeh/Notebook/PcTF Subcloning in E-coli/2012/12/18: Difference between revisions
From OpenWetWare
Line 16: | Line 16: | ||
'''Plate Reader''' | '''Plate Reader''' | ||
* Transfer 50 μl of each solution to the Costar 96 clear bottom black side. | * Transfer 50 μl of each solution and a control to the Costar 96 clear bottom black side. | ||
* Here is the software setting: | * Here is the software setting: | ||
** Fluorescence | ** Fluorescence | ||
Line 28: | Line 28: | ||
** Read Height: 9.5 mm | ** Read Height: 9.5 mm | ||
* Click OK and then Run the experiment. | * Click OK and then Run the experiment. | ||
* Export the data to an excel file. | |||
* The software will deduce the control data from the sample data | |||
'''Result''' | '''Result''' |
Revision as of 14:23, 18 December 2012
PcTF Subcloning in E. coli | <html><img src="/images/9/94/Report.png" border="0" /></html> Main project page <html><img src="/images/c/c3/Resultset_previous.png" border="0" /></html>Previous entry<html> </html>Next entry<html><img src="/images/5/5c/Resultset_next.png" border="0" /></html> | ||||||||||||
18/12/2012RFP Plate Reader Serial Dilution
Plate Reader
Result
|