Difference between revisions of "Team:elan vital korea/Protocol"
Line 365: | Line 365: | ||
<P style="text-align:left;"> | <P style="text-align:left;"> | ||
<font color="white"> | <font color="white"> | ||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
<h5 style="text-align:center;"> | <h5 style="text-align:center;"> | ||
</a><font color="black">LB Agar Plates and Addition of Antibiotics</font></h5> <br> | </a><font color="black">LB Agar Plates and Addition of Antibiotics</font></h5> <br> |
Revision as of 13:13, 14 September 2015
PROTOCOL
We conducted our experiments by following the protocols below. As an official procedure, lab workers should understand the lab experiment
assigned to them along with safety procedures before starting lab work. The protocols are arranged according to the order of experiments we followed.
Protocols to handle enzymes.
Protocols to store materials and maintain
usage history of each material.
To The Top
1.
7. Process
1. We used LB medium almost every day, so we have
prepared LB medium many times. To prevent
contamination, we only used LB medium made within
three days.
2. Materials: NaCl, Trypton, Yeast Extract, and ddH2O (triple
distilled water)
3. Equipment: autoclave, electronic scale.
4. Process
We usually make 200 liter LB bottle
1) 2 g of NaCl to a final concentration of 0.17 M
2) 2g of 1%(w/v) Bacto™ tryptone
3) 1g of 0.5% (w/v) yeast extract
4) ddH2O to 200 mL
5) Autoclave for 20 min within 2 hours
6) Keep at room temperature
LB Agar Plates and Addition of Antibiotics
We have used LB (solidified lysogeny broth), rich growth medium for E.coli, in our experiments almost all the time.
2.
All the needed chemicals including yeast extract must be prepared beforehand.
3.
Autoclave must be available.
4.
Growth on LB Agar plates provides colonies originating from one single bacteria cell.
5.
Just before pouring the solution into petri dishes, an antibiotic can be added for resistance selection.
We
followed the normal working concentrations such as:
- chloramphenicol: 25 μg/mL
(Chloramphenicol stock is dissolved in ethanol)
In case of using ampicillin: 100 μg/mL
- normal stock concentrations:1000-fold
6. Material to make LB plates:
NaCl (Sodium Chloride)
Bacto™ tryptone
yeast extract
Bacto™ agar
ddH2O (triple distilled water)
1000x chloramphenicol or ampicillin
To The Top
We usually make 1liter bottle for LB Agar
1) 200 mL LB prepared fresh, non-autoclaved
2) 3 g agar
3) Shake until all solids are dissolved
4) Autoclave for 20 min within 2 hr
5) Keep it cool until it reaches around 40-50 °C
6) Add 200 μL of 1000x chloramphenicol and gently stir it. Be careful not to shake the bottle too long/hard so that
bubbles are created.
7) Pour into empty petri dishes just enough to cover the surface (~20 mL per plate). In case that bubbles are in
the plate, heat the plate surface carefully with a burner only until the bubbles are burst but the solution is
heated.
8) Leave the plates at room temperature around one hour until it is solidified.
9) Solidified plates should be turned upside down for a few hours at room temperature, then stored at 4°C.
LB Medium
Overnight Cultures with Antibiotics