13/08/13

From 2013.igem.org

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(Created page with "==Making agar, chloroamphenicol and chloroamphenicol/IPTG plates==")
(Agarose gel preparation)
 
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{| style="color:#87EA00;background-color:#FFFFFF;" cellpadding="2" cellspacing="2" border="0" bordercolor="#000000" width="100%" align="center"
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!align="center"|[[Team:Leicester|Home]]
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!align="center"|[[Team:Leicester/Team|Team]]
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!align="center"|[https://igem.org/Team.cgi?year=2013&team_name=Leicester Official Team Profile]
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!align="center"|[[Team:Leicester/Project|Project]]
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!align="center"|[[Team:Leicester/Parts|Parts Submitted to the Registry]]
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!align="center"|[[Team:Leicester/Modeling|Modeling]]
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!align="center"|[[Team:Leicester/Notebook|Notebook]]
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!align="center"|[[Team:Leicester/Safety|Safety]]
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!align="center"|[[Team:Leicester/Attributions|Attributions]]
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|}
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</div>
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==Making agar, chloroamphenicol and chloroamphenicol/IPTG plates==
==Making agar, chloroamphenicol and chloroamphenicol/IPTG plates==
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*One container of 400 ml Luria Agar was melted down in the microwave. This is enough to make 20 agar petri dishes.
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*This was poured straight into 4 petri dishes to make agar plates
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*The remaining agar had 0.64 ul  of chloroamphenicol added to it (concentration = 24 ug/ml), and was mixed thoroughly
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*The resulting solution was poured into 4 petri dishes, to make 4 chloroamphenicol agar plates
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*The remaining agar solution had 1.5 ul of IPTG added to it (concentration = 24 ug/ml)
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*This was mixed thoroughly, and then used to make up the remaining 12 chloroamphenicol/IPTG plates.
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==Agarose gel preparation==
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*20 ml of 5 x TBE, 80 ml of distilled water and 0.8 g of agarose was added into a container.
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*The solution was boiled for 3 minutes, 1 minute at a time.
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*The solution was left to cool.
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*5 ul of ethidium bromide was added to the solution.
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*The solution was then poured into the gel plate and left to set for 30 minutes.

Latest revision as of 15:52, 13 August 2013

Home Team Official Team Profile Project Parts Submitted to the Registry Modeling Notebook Safety Attributions

Making agar, chloroamphenicol and chloroamphenicol/IPTG plates

  • One container of 400 ml Luria Agar was melted down in the microwave. This is enough to make 20 agar petri dishes.
  • This was poured straight into 4 petri dishes to make agar plates
  • The remaining agar had 0.64 ul of chloroamphenicol added to it (concentration = 24 ug/ml), and was mixed thoroughly
  • The resulting solution was poured into 4 petri dishes, to make 4 chloroamphenicol agar plates
  • The remaining agar solution had 1.5 ul of IPTG added to it (concentration = 24 ug/ml)
  • This was mixed thoroughly, and then used to make up the remaining 12 chloroamphenicol/IPTG plates.

Agarose gel preparation

  • 20 ml of 5 x TBE, 80 ml of distilled water and 0.8 g of agarose was added into a container.
  • The solution was boiled for 3 minutes, 1 minute at a time.
  • The solution was left to cool.
  • 5 ul of ethidium bromide was added to the solution.
  • The solution was then poured into the gel plate and left to set for 30 minutes.