IGEM:MIT/2007/Notebook/2007-6-14

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9 Transformations<br>
9 Transformations<br>
<pre>
<pre>
-
Contents    Volume
+
Contents    Volume   Label
-
U V     (2 uL)
+
U V         (2 uL)   I
-
dV     (5 uL)
+
dV         (5 uL)   A
-
dV + dI   (5 uL)
+
dV + dI     (5 uL)   B
-
ddV       (5 uL)
+
ddV         (5 uL)   C
-
ddV + ddI   (5 uL)
+
ddV + ddI   (5 uL)   D
-
dV       (10 uL)
+
dV         (10 uL)   E
-
dV + dI     (10 uL)
+
dV + dI     (10 uL)   F
-
ddV     (10 uL)
+
ddV         (10 uL)   G
-
ddV + ddI     (10 uL)
+
ddV + ddI   (10 uL)   H
</pre><br><br>
</pre><br><br>

Revision as of 09:59, 14 June 2007

Grad Advisors

  • Morning: Debbie
  • Afternoon: Brian

LAB WORK

  • Make competent E. coli cells
  • Transformation into competent cells
  • Plate transformed cells


Depending on how fast cells grow......

  • Night time
    • Analyze plates
    • innoculate 4ml LB/Amp

Procedures

Details of DH5 Strain E Coli

Regular cell membranes are not permeable to plasmids, so we much use ions (CaCl) to make the bacteria competent and able to accept foreign DNA.
Start: 2 vials of competent bacteria (500 uL each)
9 Transformations

Contents    Volume    Label
U V         (2 uL)    I
dV          (5 uL)    A
dV + dI     (5 uL)    B
ddV         (5 uL)    C
ddV + ddI   (5 uL)    D
dV          (10 uL)   E
dV + dI     (10 uL)   F
ddV         (10 uL)   G
ddV + ddI   (10 uL)   H


  1. Aliquot 5 uL and 10 uL of ligation reactions into eppendorfs
    • For the undigested vector, dilute 100x so we can put in around 2 ng (because optical density of undigested vector is 86.4 ng/uL)
  2. Pipette 50 uL of competent DH5a E. coli bacteria into ligation reaction plasmid eppendorfs from above and mix by tapping gently
    • Do not pipette up and down
  3. Incubate on ice for 60 minutes
  4. Heat shock the bacteria in a 37C water bath for 30 seconds
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