Team:UNIPV-Pavia/Protocols/AntarcticPhosphatase
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*[[Team:UNIPV-Pavia/Protocols/Digestion|BioBrick digestion with restriction enzymes]] | *[[Team:UNIPV-Pavia/Protocols/Digestion|BioBrick digestion with restriction enzymes]] | ||
*[[Team:UNIPV-Pavia/Protocols/GelExtraction|DNA gel extraction]] | *[[Team:UNIPV-Pavia/Protocols/GelExtraction|DNA gel extraction]] | ||
+ | *[[Team:UNIPV-Pavia/Protocols/Precipitation|DNA precipitation with sodium acetate]] | ||
*[[Team:UNIPV-Pavia/Protocols/AntarcticPhosphatase|Antarctic Phosphatase]] | *[[Team:UNIPV-Pavia/Protocols/AntarcticPhosphatase|Antarctic Phosphatase]] | ||
*[[Team:UNIPV-Pavia/Protocols/Ligation|Ligation]] | *[[Team:UNIPV-Pavia/Protocols/Ligation|Ligation]] | ||
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- | <h1> | + | <h1>Antarctic Phosphatase</h1> |
- | ''(estimated time: | + | ''(estimated time: 1 hour and 30 min)'' |
<br> | <br> | ||
<br> | <br> | ||
'''Materials needed:''' | '''Materials needed:''' | ||
- | *''' | + | *'''NEB Antarctic Phosphatase''' |
- | *''' | + | *'''10X NEB Antarctic Phosphatase buffer''' |
+ | *'''Cut and gel-extracted vector''' | ||
<br> | <br> | ||
- | * | + | *Add the proper amount of 10X buffer to a final concentration of 1X (e.g. 2 µl of 10X buffer in a final volume of 20 µl). |
- | * | + | *Add 1 µl of Antarctic Phosphatase (up to 5 µg of cut vector). |
- | + | *Incubate at 37°C for 1 hour (Antarctic Phosphatase works). | |
- | * | + | *Incubate at 65°C for 15 min (Antarctic Phosphatase inactivation). |
- | *Incubate at | + | |
- | + | ||
<br> | <br> |
Latest revision as of 12:53, 1 July 2008
Home | The Team | The Project | Biological Safety | Parts Submitted to the Registry |
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Dry Lab | Wet Lab | Modeling | Protocols | Activity Notebook |
The protocols we used
- LB medium preparation
- Plasmid resuspension from IGEM paper spots
- Transformation
- Plasmid extraction
- BioBrick digestion with restriction enzymes
- DNA gel extraction
- DNA precipitation with sodium acetate
- Antarctic Phosphatase
- Ligation
- PCR
Antarctic Phosphatase
(estimated time: 1 hour and 30 min)
Materials needed:
- NEB Antarctic Phosphatase
- 10X NEB Antarctic Phosphatase buffer
- Cut and gel-extracted vector
- Add the proper amount of 10X buffer to a final concentration of 1X (e.g. 2 µl of 10X buffer in a final volume of 20 µl).
- Add 1 µl of Antarctic Phosphatase (up to 5 µg of cut vector).
- Incubate at 37°C for 1 hour (Antarctic Phosphatase works).
- Incubate at 65°C for 15 min (Antarctic Phosphatase inactivation).