Team:Freiburg/Notebook/3 September

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==<span style="color:green;">green light receptor</span>==
==<span style="color:green;">green light receptor</span>==
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===NAME OF YOUR EXPERIMENT===
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===Testdigestion of 2a-assembly===
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'''Investigators:NAME'''
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'''Investigators: Julia'''
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<br/>
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Continuing from 31 of Aug. [https://2011.igem.org/Team:Freiburg/Notebook/31_August]<br/>
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Before Miniprep of 20 different colonies.<br/>
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Each minipreped DNA-sample (3μl)was digested with EcoRI and PstI.<br/>
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<br/>
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Result:<br/>
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<br/>
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[[File:Freiburg11 09 03Testdigest 2A.Jpg|400px|400px]]
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<br/>
 +
 
 +
 
 +
 
 +
the samples
 +
 
 +
46b= ho1 with a RBS (BBa_B0034)<br/>
 +
 
 +
50b= RBS(BBa_B0034)+pcyA+terminator<br/>
 +
 
 +
64b= Promotor (BBa_J23110)+CcaS<br/>
 +
 
 +
67b= Promotor (BBa_J23110)+CcaR<br/>
 +
 
 +
were send on [https://2011.igem.org/Team:Freiburg/Notebook/6_September 6.09] to GATC for sequencing
 +
 
 +
===3A-assembly:Digestion===
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 +
'''Investigators: Sandra'''
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Digestion of:
 +
 
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'''InsertI:'''
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*64, CcaR
 +
*46, ho1
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 +
with EcorI and SpeI
 +
 
 +
'''InsertII:'''
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*67, CcaS
 +
*50, pcyA
 +
 
 +
with XbaI and PstI
 +
 
 +
For this assembly we used the constructs from the 2A-assembly made on [https://2011.igem.org/Team:Freiburg/Notebook/31_August 31.08]
 +
 
 +
Incubation for 6 hours at 37°C. Vector pSB1C3 was already digested,<br/>  it was just treated with antarctic phosphatase for one hour.
 +
===3A-assembly:Ligation===
 +
'''Investigators: Julia'''
==<span style="color:blue;">blue light receptor</span>==
==<span style="color:blue;">blue light receptor</span>==
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===NAME OF YOUR EXPERIMENT===
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===Stop of ligation===
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'''Investigators:NAME'''
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'''Investigators: Sandra'''
 +
Inactivation of ligase at 80°C for 20 minutes.<br/>
 +
Stored in the blue light box, labelled: ♥C3 Lig., and Not C3 Lig.
 +
To do: Trafo
 +
 +
===Transformation===
 +
with ♥C3 Lig. and Not C3 Lig
 +
 +
'''Investigator: Sophie'''
==<span style="color:red;">red light receptor</span>==
==<span style="color:red;">red light receptor</span>==
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==<span style="color:grey;">Precipitator</span>==
==<span style="color:grey;">Precipitator</span>==
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===NAME OF YOUR EXPERIMENT===
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===Picking clones===
 +
 
 +
'''Investigators: Sandra'''
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 +
Only few colonies grew on two plates. These clones were picked and incubated in LB with amp at 37°C.
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'''Investigators: NAME'''
 
{{:Team:Freiburg/Templates/footer}}
{{:Team:Freiburg/Templates/footer}}

Latest revision as of 00:27, 22 September 2011


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

Contents

green light receptor

Testdigestion of 2a-assembly

Investigators: Julia
Continuing from 31 of Aug. [1]
Before Miniprep of 20 different colonies.
Each minipreped DNA-sample (3μl)was digested with EcoRI and PstI.

Result:

Freiburg11 09 03Testdigest 2A.Jpg


the samples

46b= ho1 with a RBS (BBa_B0034)

50b= RBS(BBa_B0034)+pcyA+terminator

64b= Promotor (BBa_J23110)+CcaS

67b= Promotor (BBa_J23110)+CcaR

were send on 6.09 to GATC for sequencing

3A-assembly:Digestion

Investigators: Sandra

Digestion of:

InsertI:

  • 64, CcaR
  • 46, ho1

with EcorI and SpeI

InsertII:

  • 67, CcaS
  • 50, pcyA

with XbaI and PstI

For this assembly we used the constructs from the 2A-assembly made on 31.08

Incubation for 6 hours at 37°C. Vector pSB1C3 was already digested,
it was just treated with antarctic phosphatase for one hour.

3A-assembly:Ligation

Investigators: Julia

blue light receptor

Stop of ligation

Investigators: Sandra

Inactivation of ligase at 80°C for 20 minutes.
Stored in the blue light box, labelled: ♥C3 Lig., and Not C3 Lig.

To do: Trafo


Transformation

with ♥C3 Lig. and Not C3 Lig

Investigator: Sophie

red light receptor

NAME OF YOUR EXPERIMENT

Investigators:NAME



Lysis cassette

NAME OF YOUR EXPERIMENT

Investigators:NAME


Precipitator

Picking clones

Investigators: Sandra

Only few colonies grew on two plates. These clones were picked and incubated in LB with amp at 37°C.

                       

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