Team:NTU-Singapore/Notebook/4 July 2008

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Latest revision as of 02:24, 28 October 2008


Contents

Friday 4 July

Hung, Darius

    • Ligation of E7 into empty plasmid vector extracted from GFP plasmid.
      • Gel electrophoresis for the E7 plasmids synthesized by PCR (with 2 blunt ends recognized by EcoRI and PstI).
      • Gel extraction of E7 bands (around 2kb) to remove all the oligonucleotides.
      • Purification for E7 after extracted.
      • Digestion of GFP by EcoRI and PstI. Incubation for 3 hours.
      • Digestion of purified E7 by EcoRI and PstI. Incubation for 3 hours.
      • Gel electrophoresis and gel extraction for GFP to get the empty plasmid vector (around 2kb).
      • PCR purification for digested E7 to remove all the enzymes, buffers and small nucleotides.
      • Ligation of empty plasmid (from GFP) and E7 insert.
      • Transformation and cloning into homemade top10 cells.

Lu Chao, Hung

transformation and cell cloning of LacI-GFP and LacI-RFP again.

Lu Chao

inoculation of LacI-RBS cells.

Choon Kit

documentation of lab protocols.