Team:Goettingen/week5-3

From 2012.igem.org

Revision as of 09:49, 22 September 2012 by Alicia (Talk | contribs)

Deutsch  / English 

#3 Chemoreceptor Library - 5th Week

Back to overview

V05_29


Insertion of tar into pUC18
  • Experiment:
    Double digest of tar and pUC18 using EcoRI, PstI and Orange buffer (ThermoScientific) according to protocol. Gel extraction and purification of pUC18 and tar using PeqGOLD Gelextraction Kit (Peqlab). Ligation of tar into pUC18 using T4 DNA Ligase (Thermo Scientific).


V05_30


Transformation of DH10B with pUC18_TAR construct
  • Experiment:
    Transformation was carried out according to protocol. Transformed DH10B were plated on LB-Amp plates (see here for recipe). Transformation was successful.


V05_31


Preparation of pUC18_TAR
  • Experiment:
    Inocculation of overnight cultures of 10 supposedly positive clones in liquid LB-Amp (recipe).


V06_01


Changing the XbaI site in the tar sequence via QuikChange
  • Experiment:
    DNA was prepped using PeqGOLD MiniPrep Kit (Peqlab). A DNA test digest with EcoRI and XbaI was performed according to protocol and analyzed on a 1% agarose gel. Test digest showed 8 out of 10 clones contained the construct pUC18_TAR. QuikChange PCR was performed using designed primers and Pfu Turbo polymerase (see QuikChange protocol here). Resulting construct was labeled pUC18_TAR_QC.


V06_02


Changing the XbaI site in the tar sequence via QuikChange
  • Experiment:
    DpnI digest of QuikChange PCR product to get rid of the parent plasmid.


Back to overview

↑ Back to top!