04/09/13

From 2013.igem.org

(Difference between revisions)
(Gel purification)
(Gel Electrophoresis)
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*The double digest (pSB1C3) from yesterday was run on a 1% gel.
*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.
*This was done in order to confirm that the digest worked and also to purify the pSB1C3 vector.
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[[File:igem_psb1c3_doubledigest_040913.jpg]]
==Gel purification of the pSB1C3 backbone and RFP biobrick==
==Gel purification of the pSB1C3 backbone and RFP biobrick==

Revision as of 08:37, 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

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