Team:Freiburg/Notebook/26 August

From 2011.igem.org

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==<span style="color:blue;">blue light receptor</span>==
==<span style="color:blue;">blue light receptor</span>==
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===Ligation===
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'''Investigators: Sophie'''<br/>
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Date: 25.08.11<br/>
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Experiment: Digestion <br/>
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Investigator: Sandra<br/> 
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Project Name: Blue light receptor<br/>
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all samples stored in Blue light box
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===Transformation===
===Transformation===
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'''Investigators: Sophie'''<br/>
'''Investigators: Sophie'''<br/>
Date: 26.08.11<br/>
Date: 26.08.11<br/>
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Continue from <br/>                                 Date: 26.08.11        Name: Sophie                 
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Continue from                                  Date: 26.08.11        Name: Sophie                 
Experiment Ligation <br/>   
Experiment Ligation <br/>   
Project Name: Blue light receptor<br/>
Project Name: Blue light receptor<br/>

Revision as of 12:50, 26 August 2011


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

Contents

Meeting

attendants:
Time:

green light receptor

already done:


To-do:

blue light receptor

already done:


To-do:

red light receptor

already done:


To-do:

Lysis cassette

already done:


To-do:


Precipitator

already done:


To-do:

green light receptor

NAME OF YOUR EXPERIMENT

Investigators:NAME


blue light receptor

Ligation

Investigators: Sophie
Date: 25.08.11
Experiment: Digestion
Investigator: Sandra
Project Name: Blue light receptor
all samples stored in Blue light box


Transformation

Investigators: Sophie
Date: 26.08.11
Continue from Date: 26.08.11 Name: Sophie Experiment Ligation
Project Name: Blue light receptor

Procedure
1. take cells from -80°C freezer and put them on ice! (every eppi contains about 400 μl cells) 2. thaw cells on ice 20 minutes 3. pipette 50 μl cells and 2 μl DNA into eppi still on ice! 4. Incubate for 30 minutes on ice 5. Heat at 42°C for 60 sec 6. Incubate on ice for 5 minutes 7. Add 200 μl LB Broth 8. Incubate for 2 hours at 37°C (cells with lysis cassette at 30°C!!) 9. Plate 50 μl and 200μl on two different LB/Agar plates with appropriate antibiotic resistance


Documentation: Why are you doing this experiment? Name of the sample? Where are they stored? Name the vector with inserts, antibiotika resistance etc. Why? The last cloning was done with a NOT-PCR-Product which might make problems because it does not have enough bases after the restriciton sites.

Name of the samples: Not 1:1, Not 1:3, nOt 1:1 nOt 1:3, noT 1:1, noT 1: 3

stored in incubator on Amp plates

vector: psb1A3
inserts: Not/ nOt/ noT + LOV-3A-PCR

red light receptor

NAME OF YOUR EXPERIMENT

Investigators:NAME



Lysis cassette

NAME OF YOUR EXPERIMENT

Investigators:NAME


Precipitator

NAME OF YOUR EXPERIMENT

Investigators: NAME

                       

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