Team:Imperial College London/Wetlab/Protocols/Calibration

From 2009.igem.org

(Difference between revisions)
(Calibration protocols (CA))
Line 12: Line 12:
| <b>CA2</b>:External GFP fluorescence
| <b>CA2</b>:External GFP fluorescence
| [[Team:| Link]]
| [[Team:| Link]]
-
| * T <br>
+
| * To relate how the fluorescence observed can be correlated with number of GFP molecules <br>
|- style="color:#333; background-color:#CCCCFF;" cellpadding="6" cellspacing="0" border="1"
|- style="color:#333; background-color:#CCCCFF;" cellpadding="6" cellspacing="0" border="1"
| <b>CA3</b>:Internal GFP fluorescence
| <b>CA3</b>:Internal GFP fluorescence

Revision as of 15:41, 23 September 2009

Calibration protocols (CA)

Section Assay Overview and Aims
CA1:Calibration Curves TOP10 Growth * To produce a calibration curve to aid in the normalising of absorbance values. The relation of absorbance reading to number of cells varies with different cell strains. We are therefore doing one for Top-10.
CA2:External GFP fluorescence Link * To relate how the fluorescence observed can be correlated with number of GFP molecules
CA3:Internal GFP fluorescence Link * T

Mr. Gene   Geneart   Clontech   Giant Microbes