Team:TU-Eindhoven/LabJournal

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==Lab Journal==
==Lab Journal==
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{{:Team:TU-Eindhoven/Template:Timeline | title=Creating agar plates | day=24 | month=July | year=2013 }}
{{:Team:TU-Eindhoven/Template:Timeline | title=Creating agar plates | day=24 | month=July | year=2013 }}
Before any real lab work could begin some supplies had to be created, including a selection of agar plates. We needed two different types of agar plates, some with ampicillin antibiotics and others with kanamycin antibiotics. To manage this we created 2 separate agar solutions, a 200mL mixture for the ampicillin plates and a 400mL mixture for the kanamycin plates. The protocol we followed for the creation of the agar solutions was as follows:  
Before any real lab work could begin some supplies had to be created, including a selection of agar plates. We needed two different types of agar plates, some with ampicillin antibiotics and others with kanamycin antibiotics. To manage this we created 2 separate agar solutions, a 200mL mixture for the ampicillin plates and a 400mL mixture for the kanamycin plates. The protocol we followed for the creation of the agar solutions was as follows:  

Revision as of 12:12, 25 July 2013

Lab Journal

24 July
2013
Before any real lab work could begin some supplies had to be created, including a selection of agar plates. We needed two different types of agar plates, some with ampicillin antibiotics and others with kanamycin antibiotics. To manage this we created 2 separate agar solutions, a 200mL mixture for the ampicillin plates and a 400mL mixture for the kanamycin plates. The protocol we followed for the creation of the agar solutions was as follows:

  • Mix together the following amounts to create 200mL agar solution:
    • 2g Peptones
    • 2g NaCl
    • 1g Yeast extract
    • 3g Agar
    • Fill the container up to 200mL with demineralised water.
  • For a 400mL solution mix together:
    • 4g Peptones
    • 4g NaCl
    • 2g Yeast extract
    • 6g Agar
    • Fill the container up to 400mL with demineralised water.
  • Next the containers were autoclaved and allowed to cool, but not harden.
  • The following steps were all performed in the vicinity of a blue flame to ensure a sterile working environment.
  • Before pouring the plates the correct antibiotics were added. The concentration of the ampicillin antibiotics was 100ηg/µL and that of the kanamycin antibiotics was 30ηg/µL.
  • The solutions were now ready to be poured into agar plates. From the solutions we made we were able to pour 8 ampicillin plates and after receiving a little extra (about 350mL) kanamycin agar solution we poured a total of 22 kanamycin plates.
  • The plates were cooled on the bench and allowed to harden before being stored in a 4° refrigerator.

25 July
2013


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