Team:Bielefeld-Germany/Labjournal/May

From 2013.igem.org

(Difference between revisions)
Line 4: Line 4:
__NOTOC__
__NOTOC__
-
 
<div id=globalwrapper style="padding-left:20px; padding-right:20px">
<div id=globalwrapper style="padding-left:20px; padding-right:20px">

Revision as of 21:39, 4 October 2013



May


Milestones

  • Initiating lab work on the sub-project endogenous mediator Glycerol dehydrogenase.
  • Starting lab work with the first successful PCR: GldA with Pre- and Suffix overlaps could be amplified from Escherichia coli genome.
  • The main work however is still planning of our subprojects, designing experiments and a lot of research.
  • Finding sponsors goes ahead. Many companies like our project and want to support us.






Week 1

Organization

  • We were already able to find sponsors for our team: IIT BIEKUBA, IIT Biotech, Evonik, PlasmidFactory and FisherScientific will support us.


MFC

Mediators

  • Glycerol dehydrogenase
    • Primerdesign for isolation of GldA gene from Escherichia coli KRX strain, with overlaps for BioBrick Prefix and Suffix:
    • Forward Primer GldA (43 bp): GAATTCGCGGCCGCTTCTAGATGGACCGCATTATTCAATCACC
    • Reverse Primer GldA (45 bp): CTGCAGCGGCCGCTACTAGTATTATTCCCACTCTTGCAGGAAACG










2.Week

Organization

  • Distribution of our team in various subgroups for best work efficiency.
  • We’ve organized a barbecue to thank the working group of Dr. Jörn Kalinowski in the CeBiTec for the appropriation of space and support in the laboratory.


MFC









3.Week

Organization

  • Planning the trip to the European jamboree in Lyon from October 11. to 13. 2013.


MFC

Mediators

  • Glycerol dehydrogenase


Table 1: Standard Phusion PCR Master Mix.

Table 2: Two step standard Phusion PCR program for GldA amplification.


    • GldA PCR product was isolated by agarose gel electrophoresis and purified.
    • Bands are on at the expected size of 1050 bp.


Figure 1: Agarose gel from PCR on the GldA gene of Escherichia coli KRX strain with forward and reverse primer GldA. As a ladder we used [http://www.thermoscientificbio.com/nucleic-acid-electrophoresis/generuler-1-kb-dna-ladder-ready-to-use-250-to-10000-bp GeneRuler™ 1 kb DNA Ladder from Thermo Scientific].










4.Week

Organization

  • We will also take part at the congress "Next generation of biotechnological processes 2020+" in Berlin at 27. June 2013.
  • Having a second presentation at Merck KGaA head office in Darmstadt for explaining our project in detail. We are happy that Merck will be our next supporter in 2013.


MFC











Contents