Team:Calgary/Notebook/Protocols/Process19

From 2011.igem.org

(Difference between revisions)
 
(3 intermediate revisions not shown)
Line 1: Line 1:
{{Team:Calgary/Main_Header|notebook}}
{{Team:Calgary/Main_Header|notebook}}
{{Team:Calgary/Notebookbar|
{{Team:Calgary/Notebookbar|
-
TITLE=cDNA Synthesis/Reverse Transcription Reaction|
+
TITLE=Making Chemically Competent <i>E. coli</i> Cells|
BODY=<html>
BODY=<html>
-
<br /> <br /> <h2 style="color:#0066CC">Making competent cells</h2>
 
-
<br /> <p>This procedure was done using Top10 cells ordered from Invitrogen. 50 mL Falcon tubes were used for this protocol.</p>
+
 
 +
<p>This procedure was done using Top10 cells ordered from Invitrogen. 50 mL Falcon tubes were used for this protocol.</p>
<ol>
<ol>
Line 17: Line 17:
<li> Leave on ice for at least 30 minutes and then aliquot 200 uL and freeze at -80&deg;C </li>
<li> Leave on ice for at least 30 minutes and then aliquot 200 uL and freeze at -80&deg;C </li>
</ol>
</ol>
-
 
+
<br></br><br></br>
</html>}}
</html>}}

Latest revision as of 03:24, 29 September 2011


Making Chemically Competent E. coli Cells

This procedure was done using Top10 cells ordered from Invitrogen. 50 mL Falcon tubes were used for this protocol.

  1. Innoculate 5-10 mL LB at 37°C while shaking
  2. Subculture 1 mL of bacteria solution into 50 mL LB broth at 37° while shaking until OD600 is 0.4-0.6 (This step should require approximately 2.5 hours)
  3. Centrifuge the subculture at 10 000 rpm at 4°C for 2 minutes
  4. Resuspend pellet in 12.5 mL of cold CaCl2 (50 mM) and leave on ice for 10 minutes
  5. Centrifuge at 10 000 rpm at 4°C for 2 minutes and resuspend in 2 mL of cold CaCl2 (50 mM, 15% glycerol solution)
  6. Leave on ice for at least 30 minutes and then aliquot 200 uL and freeze at -80°C