Dienstag, 14. August 2012

13.08.2012


Start-> 17:30
Origami (Alex):
  • Cost 1160 euros, 7560 bp.
  • Origami descrition see presentation and dropbox for extra details
  • Question: Why the locks are not symmetric
  • Effective radio of strands in the origami: 2.25nm, extra 0.25nm given by possible repulsion between strands.
  • 45nmx37.35x40.5-44nm
  • Two versions->guided, not guided
  • Edge staples. Possible correction issues.
  • Versions tried->Open shell, closed shell
  • Separation by gel extraction->Doesn’t it damage the structure???
  • IDEA: PCR Purification to separate single oligos from structure.
  • Staining->which technique use Douglas for staining?
  • Different protocols for staining 3 drops of water, 1 drop. Which one is the best??
  • Is DNA interacting with the grid?? Maybe as it is laying It can change its structure and affect the results. Check with Douglas paper.
  • Results->Good: Distinguishable regular spots, Bad: No differentiation between open and closed versions
  • Errors in staining->probably during centrifugation and taking too much time.
  • We should do a gel with different buffers, i.e, different concentrations of Mg(2+).
  • Probable clash between Mg concentrations for DNA and GUV experiments.
  • Maybe adding long catcher strands could help the structure to stay open.
  • Schedule staining session with Suzanne Kretschmar and TEM session with Thomas Kurth.
  • Question: How is DNA labeled?? Could we use QDots??
Santiago part/Wiki and Origami:
  • Origami->Santiago has to be aware of every single detail of the DNA origami, know the sequences, structure of the origami, length, locks, guide strands.
  • Gockan designed the webpage for I-GEM. He knows a lot about javascripting and Photoshop. Contact him!! Use I-Gem web pages as a measuring stick for webpage. BIOMOD ones are not that good.
Finances:
  • Who’s gonna do the finances? -> Varsha
  • Tell to juliane, avoid any confusion for her.
GUVs:
  • Problem-> Still clustering.
  • Possible solutions-> Change buffer concentration and length of the linker
  • LSM meeting tomorrow at 10:00->Praveen, Varsha and Mari are attending
  • Aptamer group-> Ali should check the kinetic coefficients and know them by heart, not just saying that they’re on the paper.
  • We have to know things to order from the sponsorship of the companies-> we have to do it fast; if it’s too late companies could be reluctant to give them.
  • Start Downloading the pictures made with the LSM for safety issues

Keine Kommentare:

Kommentar veröffentlichen