04/09/13

From 2013.igem.org

(Difference between revisions)
(Gel Electrophoresis)
(Gel Electrophoresis)
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*This was done in order to confirm that the digest worked and also to purify the pSB1C3 vector.
*This was done in order to confirm that the digest worked and also to purify the pSB1C3 vector.
[[File:igem_psb1c3_doubledigest_040913.jpg]]
[[File:igem_psb1c3_doubledigest_040913.jpg]]
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*From left to right
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#Sample 1.1 - track 2
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#Sample 1.2 - track 3
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#Sample 2.1 - track 4
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#Sample 2.2 - track 5
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**The 2 Kb bands are the pSB1C3 backbone
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**The 1 Kb bands are the RFP biobrick
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The two higher bands in tracks 2 and 3 are plasmids that were not digested.
==Gel purification of the pSB1C3 backbone and RFP biobrick==
==Gel purification of the pSB1C3 backbone and RFP biobrick==

Revision as of 08:47, 5 September 2013

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Contents

Transformation results

Gel Electrophoresis

  • The double digest (pSB1C3) from yesterday was run on a 1% gel.
  • This was done in order to confirm that the digest worked and also to purify the pSB1C3 vector.

Igem psb1c3 doubledigest 040913.jpg

  • From left to right
  1. Sample 1.1 - track 2
  2. Sample 1.2 - track 3
  3. Sample 2.1 - track 4
  4. Sample 2.2 - track 5
    • The 2 Kb bands are the pSB1C3 backbone
    • The 1 Kb bands are the RFP biobrick
The two higher bands in tracks 2 and 3 are plasmids that were not digested.

Gel purification of the pSB1C3 backbone and RFP biobrick

  • The Zymoclean Gel DNA recovery Kit was used to perform the purification and its protocol was followed.
  • However the elution step was changed to 12ul of elution buffer, and this step was repeated.

Double digest of TOD gene ligations