Team:UNIPV-Pavia/Methods Materials/Resuspension
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(New page: {{UNIPV-Pavia/Protocols}} <br> == '''DNA resuspension from iGEM 2009 plates''' == ''(Estimated time: 30 min)'' <br> <br> '''Materials needed:''' *'''iGEM 2009 plates''' *'''PC with intern...) |
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+ | <html> | ||
+ | <head> | ||
+ | <link rel="stylesheet" type="text/css" href="http://bioinfo.unipv.it/igem/templates/SpryAssets/SpryMenuBar.js" title="Stile"/> | ||
+ | </head> | ||
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+ | <table width="100%"> | ||
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+ | <td align="center"> | ||
+ | <img width="100%" height="180px" src="https://static.igem.org/mediawiki/2009/c/c2/UNIPV_title_MandM.jpg" ></img> | ||
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+ | <table width="100%"> | ||
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+ | {{UNIPV-Pavia/Menu}} | ||
+ | </td> | ||
+ | <html> | ||
+ | <td width="50%"></td> | ||
+ | <td align="center"><br><bR> | ||
+ | <font face="Pristina" size="50" ><b>Protocols</b></font> | ||
+ | </td> | ||
+ | </html> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td> {{UNIPV-Pavia/Protocols}}</td> | ||
+ | </tr> | ||
+ | </table> | ||
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+ | |||
+ | <br> | ||
+ | == '''LB medium''' == | ||
+ | ''(Estimated time: 10 min + 4 hours of autoclavation and cooling)'' | ||
+ | <br> | ||
+ | <br> | ||
+ | '''Materials needed:''' | ||
+ | *'''NaCl''' | ||
+ | *'''BactoTryptone''' | ||
+ | *'''Yeast extract ''' | ||
+ | *'''ddH2O''' | ||
+ | *'''Agar''' | ||
+ | *'''Clean bottle or E-flask''' | ||
+ | <br> | ||
+ | *For a final volume of 1 l, put: | ||
+ | **10 g NaCl | ||
+ | **10 g BactoTryptone | ||
+ | **5 g Yeast extract | ||
+ | **15 g Agar (only for LB plates) | ||
+ | *into 1 l of ddH2O. | ||
+ | *Autoclave the solution. | ||
+ | *Let it cool to ~40-45°C | ||
+ | *Add the proper antibiotic if needed. | ||
+ | *ONLY FOR PLATES: | ||
+ | **Pour an homogenous layer of agar LB into Petri plates under the hood. | ||
+ | **Let agar LB polymerase. | ||
+ | *Cover and store at +4°C. | ||
+ | *Always check for contaminations before using! | ||
+ | <br> | ||
+ | |||
<br> | <br> | ||
== '''DNA resuspension from iGEM 2009 plates''' == | == '''DNA resuspension from iGEM 2009 plates''' == |
Revision as of 17:17, 22 June 2009
LB medium
(Estimated time: 10 min + 4 hours of autoclavation and cooling)
Materials needed:
- NaCl
- BactoTryptone
- Yeast extract
- ddH2O
- Agar
- Clean bottle or E-flask
- For a final volume of 1 l, put:
- 10 g NaCl
- 10 g BactoTryptone
- 5 g Yeast extract
- 15 g Agar (only for LB plates)
- into 1 l of ddH2O.
- Autoclave the solution.
- Let it cool to ~40-45°C
- Add the proper antibiotic if needed.
- ONLY FOR PLATES:
- Pour an homogenous layer of agar LB into Petri plates under the hood.
- Let agar LB polymerase.
- Cover and store at +4°C.
- Always check for contaminations before using!
DNA resuspension from iGEM 2009 plates
(Estimated time: 30 min)
Materials needed:
- iGEM 2009 plates
- PC with internet connection :-)
- ddH20
- 0.5 ml sterile Eppendorf tubes
- Find the correct position of the desired DNA from the iGEM 2009 plates
- Resuspend with ddH20 and transfer in an Eppendorf tubes
- Store at -20°C