Team:UNICAMP-Brazil/Notebooks/September 13

From 2009.igem.org

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(Lysozyme (orf), Jen1 (orf), DLD (promoter) and Jen1 (promoter))
(Lysozyme (orf), Jen1 (orf), DLD (promoter) and Jen1 (promoter))
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====Lysozyme (orf), Jen1 (orf), DLD (promoter) and Jen1 (promoter)====
====Lysozyme (orf), Jen1 (orf), DLD (promoter) and Jen1 (promoter)====
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* We performed miniprep to get purified these parts (Protocol 2).  
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* We performed miniprep to get purified the plasmids containing these parts. (Protocol 2).  
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* We then digest the plasmids obtained by the miniprep with ''Xba''I (Protocol x).  
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* We then digest the plasmids obtained by the miniprep with ''XbaI'' to confirm the correct ligation of the parts following the biobrick format (Protocolo x). However, the electrophoresis gel (down) showed no success in the ligations.
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* The electrophoresis gel (down) showed nonspecific bands of al the parts digested.  
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[[Image:MInipreps e digestões Wesley.jpg |center|‎]]
[[Image:MInipreps e digestões Wesley.jpg |center|‎]]

Revision as of 20:43, 26 September 2009

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ColiGuard

finO+pSB1A3

  • After the O/N period, today we transformed the ligation finO+pSB1A3 into electrocompetent E. coli bacteria, strain DH10B. We followed protocol 3, without modifications (see Protocols section).
  • We then plated the transfomed cells in LB-AMP media, and let them grow at 37ºC for an O/N period.

finP+pSB1A3

  • We followed the same produce for the finP+pSB1A3 ligation.

Marcelo

YeastGuard

Lysozyme (orf), Jen1 (orf), DLD (promoter) and Jen1 (promoter)

  • We performed miniprep to get purified the plasmids containing these parts. (Protocol 2).
  • We then digest the plasmids obtained by the miniprep with XbaI to confirm the correct ligation of the parts following the biobrick format (Protocolo x). However, the electrophoresis gel (down) showed no success in the ligations.
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Wesley and Gleidson