Team:Freiburg/Notebook/23 August

From 2011.igem.org

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'''Investigators: Sophie:'''
'''Investigators: Sophie:'''
LOV-pcr, NOT-pcr and the Amp vector where ligated at 16°C
LOV-pcr, NOT-pcr and the Amp vector where ligated at 16°C
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===Ligation===
 
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'''Investigators: Sophie''' I ligated the purified inserts to the vector in the ratio 5:2 and 10:5 because of the loss of DNA due to the gelextraction
 
===Transformation===
===Transformation===

Revision as of 09:54, 24 August 2011


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

Contents

green light receptor

PCR

Investigator: Jakob


PCR


Name:

Jakob

Date:

16.08.2011

Continue from Experiment: 12.08.2011

Order primers

Project Name:

Quickchange of CcaR (EcoRI)

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 P 77 (1:10)
2.5µl Primer dw P 78 (1:10)
1µl dNTPs of Template DNA
1µl DNA-Template CcaR from synechocystis 5ng/µl
0.5 µl Phusion (add in the end)

The program we used: for Quickchange of CcaR (EcoRI)


Temp.
Time
Nr. of cycles
94°
5’
1x
94°
30’’
2x
64°
30’’
72°
1’30’’
94°
30’’
2x
62°
30’’
72°
1’30’’
94°
30’’
5x
61,6°
30’’
72°
1’30’’
94°
30’’
25x
57,8°
30’’
72°
1’30’’
72°
7’
1x
4°
∞


blue light receptor

Gel purification

Investigators:Sophie the bands of LOV-pcr and NOT-pcr where purificated. The vector was digested again because the band on the gel was not intense enough.

Ligation

Investigators: Sophie: LOV-pcr, NOT-pcr and the Amp vector where ligated at 16°C

Transformation

Investigators: Sophie: Transformation with the ligation product

red light receptor

PCR

Investigator: Jakob


PCR


Name:

Jakob

Date:

16.08.2011

Continue from Experiment: 12.08.2011

Order primers

Project Name:

Red light receptor, amplify Cph8

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 P 58 (1:10)
2.5µl Primer dw P 59 (1:10)
1µl dNTPs of Template DNA
1µl DNA-Template JT122 5ng/µl
0.5 µl Phusion (add in the end)

The program we used: for Cph8



Temp.
Time
Nr. of cycles
94°
5’
1x
94°
30’’
2x
68°
30’’
72°
2’30’’
94°
30’’
2x
67°
30’’
72°
2’30’’
94°
30’’
5x
66°
30’’
72°
2’30’’
94°
30’’
25x
65°
30’’
72°
2’30’’
72°
7’
1x
4°
∞

Lysis cassette

NAME OF YOUR EXPERIMENT

Investigators:NAME


Precipitator

NAME OF YOUR EXPERIMENT

Investigators: NAME

                       

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