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Project
2D Biosensor
The REACh Construct
Modeling
WatsOn
Galectin-3
OD/F Device
Parts
Achievements
Interlab Study
Policy & Practices
Kaiser-Karls-Gymnasium
NEAnderLab
MakerFaire
Safety
Economical View
BBa Intellectual Property
Blog
Collaborations
Aachen Meetup
Bielefeld
Braunschweig
Freiburg
Heidelberg
Notebook
Wetlab
Protocols
Engineering
Software
Equipment
Abbreviations
Team
Members
Instructors
Partners
Attributions
Mr Holmes
Contents
1
Media
1.1
LB medium
1.2
Hartmans minimal medium (HM)
2
Agar Chips
3
Transformation
3.1
Heat Shock
3.2
Electroporation
4
PCR
4.1
Colony PCR
4.2
QuikChange
5
Clonings
5.1
Restriction Digest
5.2
Ligation
5.3
Gibson Assembly
Media
LB medium
weight components
5 g/L NaCl
10 g/L tryptone
5 g/L yeast extract
(15 g/L agar for plates)
fill up to 1 L with deionized water
mix well
by shaking
autoclave
autoclaving tape, caps slightly unscrewed
base of the pot has to be covered with deionized water
close lid
heat
level 3 until the pressure valve opens
reduce
heat level to 1.5
set timer to
20 minutes
turn heater off
wait until the pressure valve retracts
(30-45 minutes)
open, close caps & shake
for plates, wait until you can touch the bottle (
<60 °C
, clean bench!)
add antibiotics and
shake
(gloves!)
Hartmans minimal medium (HM)
Agar Chips
Transformation
Heat Shock
thaw cells on ice
add 1 µl of plasmid DNA
incubate on ice for 30'
heat shock at 42 °C for 60
incubate on ice for 5'
add 200 µl of SOC media
incubate at 37 °C for 2 h
plate 20 and 200 µl on plates with the appropiate antibiotic
Electroporation
PCR
Colony PCR
QuikChange
Clonings
Restriction Digest
Ligation
Gibson Assembly