Team:USTC/Notebook
From 2008.igem.org
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!align="center"|[[Team:USTC|Home]] | !align="center"|[[Team:USTC|Home]] | ||
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!align="center"|[[Team:USTC/Project|The Project]] | !align="center"|[[Team:USTC/Project|The Project]] | ||
!align="center"|[[Team:USTC/Component|Components]] | !align="center"|[[Team:USTC/Component|Components]] | ||
+ | !align="center"|[[Team:USTC/Results|Results]] | ||
!align="center"|[[Team:USTC/Parts|Parts Submitted to the Registry]] | !align="center"|[[Team:USTC/Parts|Parts Submitted to the Registry]] | ||
!align="center"|[[Team:USTC/Notebook|Notebook]] | !align="center"|[[Team:USTC/Notebook|Notebook]] | ||
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== Calendar == | == Calendar == | ||
- | Click on any day below to see | + | Click on any day below to see how our wet-lab procedures were conducted. |
<div align="center"> | <div align="center"> | ||
<html> | <html> | ||
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- | == | + | <br> |
+ | == Standard protocols == | ||
[[USTC/Notebook/DNA sequencing|DNA sequencing]]<br /> | [[USTC/Notebook/DNA sequencing|DNA sequencing]]<br /> | ||
[[USTC/Notebook/PCR&Colony PCR |PCR&Colony PCR]]<br /> | [[USTC/Notebook/PCR&Colony PCR |PCR&Colony PCR]]<br /> | ||
- | [[USTC/Notebook/ | + | [[USTC/Notebook/Agarose Gel Electrophoresis |Agarose Gel Electrophoresis]]<br /> |
- | [[USTC/Notebook/ | + | [[USTC/Notebook/Plasmid Mini-Preps |Plasmid Mini-Preps]]<br /> |
- | [[USTC/Notebook/Restriction | + | [[USTC/Notebook/Gel Extraction |Gel Extraction]]<br /> |
+ | [[USTC/Notebook/Restriction Endonuleases Double Digestion|Restriction Endonuleases Double Digestion]]<br /> | ||
[[USTC/Notebook/DNA ligation|DNA ligation]]<br /> | [[USTC/Notebook/DNA ligation|DNA ligation]]<br /> | ||
[[USTC/Notebook/Preparing Antibiotic Stocks |Preparing Antibiotic Stocks]]<br /> | [[USTC/Notebook/Preparing Antibiotic Stocks |Preparing Antibiotic Stocks]]<br /> | ||
- | [[USTC/Notebook/Top10 chem competent cell transformation| | + | [[USTC/Notebook/Top10 chem competent cell transformation| Chem competent cell transformation]]<br /> |
+ | [[USTC/Notebook/Point mutation Quick-Change method|Point mutation: Quick-Change method]]<br /> | ||
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+ | ---- |
Latest revision as of 14:53, 29 October 2008
Home | The Team | The Project | Components | Results | Parts Submitted to the Registry | Notebook |
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Calendar
Click on any day below to see how our wet-lab procedures were conducted.
Standard protocols
DNA sequencing
PCR&Colony PCR
Agarose Gel Electrophoresis
Plasmid Mini-Preps
Gel Extraction
Restriction Endonuleases Double Digestion
DNA ligation
Preparing Antibiotic Stocks
Chem competent cell transformation
Point mutation: Quick-Change method