Team:Tuebingen/NotebookAppendix

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Contents

Appendix

To complete this report we list all products and software used over the course of our project.

Constructs

backbone pRS#part #1part #2part #3
313Padh1mPR Danio rerioTadh1
313Padh1mPR Xenopus laevisTadh1
315Pfet3rox1Tadh1
315Pfet3mig1Tadh1
316Panb1lacZTadh1
316Panb1luciferaseTadh1
316Psuc2lacZTadh1
316Psuc2luciferaseTadh1

Protocols

Kits

  • Genaxxon Plasmid DNA Purification Mini Prep
  • Genaxxon Gel Extraction Mini Prep
  • Genaxxon PCR DNA Purification Mini Prep
  • Qiagen Plasmid Midi

Chemicals

We needed the following chemicals:

  • Ampicillin
    beta-lactam antibiotic
  • Agarose
    Polysaccharide, major component of Agar
  • Dimethylsulfoxid (DMSO)
    organic solvent
  • Acetic Acid
  • Ethylenediaminetetraacetic acid (EDTA)
  • Ethanol
  • TRIS
    buffer solution for enzymes
  • Nucleoside triphosphate
  • Trypton
  • Isopropanol
  • Isopropyl-β-D-thiogalactopyranosid (IPTG)
  • LB-medium
    used for growth of E.coli
  • Agar-Agar

Software

The following list of software was used in the team:

  • Unipro UGENE
    UGENE is a free open-source cross-platform bioinformatics software. We used it to construct and annotate all needed sequences, search for restriction sites and visualization.
  • Vector NTI (commercial)
    All our primers were designed using Vector NTI which is also used by our advisors.
  • BLAST
    BLAST was our main sequence search tool. It was quite useful for controlling sequence results.
  • Google Drive
    Google Drive was used for our documentation and all of our collaborative work (papers, poster, images).