Team:Imperial College London/Media
From 2010.igem.org
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- | | | + | |Fv-fragment guided input module |
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- | | | + | |Ideas on parasite detection |
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- | | | + | |Gel confirming that DNA (pSB1C3 and pSB1AK3 with BOO14) has been digested properly by PstI and EcoRI. |
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- | | | + | |Gel of PCR confirming pSB1C3 has been amplified. |
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- | | | + | |Picture estimating the concentration of purified BOO14 and pSB1C3. |
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- | | | + | |Colony PCR to detect sucessfully transformed bacteria. |
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- | | | + | |3 PCR reactions to determine the most effective protocol to amplify the CWB. |
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- | | | + | |Gel of a diagnostic digest of the vector confirming that the terminator has been inserted. |
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- | | | + | |Isolation of the promoter pVEG by gel purification. |
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- | | | + | |Determining the ratio of pSB1C3 to pVEG for ligation. |
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- | | | + | |Determining the ratio of lytC to pSB1C3 for ligation. |
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Revision as of 11:38, 16 October 2010
Video Diary |
Photos | ||
Logos | ||
The Team | ||
Brainstorming | ||
Wet Lab | ||
Surface Protein | ||
Vectors | ||
XylE | ||
Strategy | ||
Parts | ||
Detection Module | ||
Fast Response Module | ||
Output Module | ||
Human Practices | ||
School Workshops | ||