Team:Freiburg/Notebook/7 September

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'''Investigators: Sophie'''
'''Investigators: Sophie'''
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again Ligation (see 31.08.11) because I don't find the last ligation product that produced positive clones. I have to redo the Trafo because the last positive clones seem to have mutated over the last generations, probably because the pbd is toxic.  
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For pbd in iGEM C3-vector: again Ligation (see 31.08.11) because I don't find the last ligation product that produced positive clones. I have to redo the Trafo because the last positive clones seem to have mutated over the last generations, probably because the pbd is toxic.  
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<br/>
labelled: L S54-ε5-C3 1:1 / 1:3
labelled: L S54-ε5-C3 1:1 / 1:3

Revision as of 14:08, 7 September 2011


This is the wiki page
of the Freiburger student
team competing for iGEM 2011.
Thank you for your interest!

Contents

Commons

Ligation

Investigators: Sandra

Ligation of PR1-PR6 with RFP (S1b and S2a). PR1-PR6 were digested with antarctica before start of ligation. Start of ligation at 12:40. Incubation at room temperature for at least 3 hours.

Trafo

Investigators: Sandra

Trafo of:

  • PR1+GFP
  • PR2+GFP
  • PR3+GFP
  • PR4+GFP
  • PR5+GFP
  • PR6+GFP
  • PR1+50b
  • PR2+50b

green light receptor

NAME OF YOUR EXPERIMENT

Investigators:NAME


blue light receptor

no colonies on the plates

There were no colonies on the plates with ligated parts of the 2A-assembly.

Miniprep

Investigators: Sophie
yesterday two tubes with LB were inoculated with cells from our S35 glycerol stock(BBa_K322999). Today minipreps were performed.

PCR

Investigators: Sophie

Name: Sophie


Date: 07.09.11
Continue from Experiment (Date)

(Name)

Project Name: Gibson of ♥ and NOT

PCR-Mixture for one Reaction:

For a 50 µl reaction use


32,5µl H20 Name
10µl 5x Phusion Buffer of Primer
2.5µl Primer fw ♥: P97

NOT: P99

2.5µl Primer dw ♥: P98

NOT: P100

1µl dNTPs of Template DNA
1µl DNA-Template M45a,b,c (BBa_Q0400)

Miniprep of M35 (1x) amd M35b (2x) (BBa_K322999)

0.5 µl Phusion (add in the end)

Digestion with Dpn I and purification with PCR purification kit What program do you use?

First 20 cycles touchdown 69°C -0.4/cycle

next 10 cycles touchdown 72°C -0.2 per cycle


PCR products were loaded onto a gel, but there were no bands execpt for not3.

red light receptor

NAME OF YOUR EXPERIMENT

Investigators:NAME



Lysis cassette

NAME OF YOUR EXPERIMENT

Investigators:NAME


Precipitator

Trafo

Investigators: Sandra

Trafo of the already ligated parts of the pbd + Gst-vector

Ligation

Investigators: Sophie

For pbd in iGEM C3-vector: again Ligation (see 31.08.11) because I don't find the last ligation product that produced positive clones. I have to redo the Trafo because the last positive clones seem to have mutated over the last generations, probably because the pbd is toxic.
labelled: L S54-ε5-C3 1:1 / 1:3
stored in "Ligationsreaktionen"-box

                       

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