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<li><a href="#Week6" class="table">Week 6: June 27 - July 3</a></li> | <li><a href="#Week6" class="table">Week 6: June 27 - July 3</a></li> | ||
<li><a href="#Week7" class="table">Week 7: July 5 - July 8</a></li> | <li><a href="#Week7" class="table">Week 7: July 5 - July 8</a></li> | ||
+ | <li><a href="#Week8" class="table">Week 8: July 11 - July 17</a></li> | ||
</ul> | </ul> | ||
</div> | </div> | ||
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</ul> | </ul> | ||
<a href="https://static.igem.org/mediawiki/2016/d/d7/T--Pittsburgh--NotebookWeek7.pdf" target="_blank">Week 7 Notebook</a><br> | <a href="https://static.igem.org/mediawiki/2016/d/d7/T--Pittsburgh--NotebookWeek7.pdf" target="_blank">Week 7 Notebook</a><br> | ||
+ | <a href="#Top">Back to Top</a> | ||
+ | |||
+ | <h1 class="nav"><a name="Week8" class="nav">Week 8: July 11 - July 17</a></h1> | ||
+ | <h2>Wet Lab</h2> | ||
+ | <h3>Reporter</h3> | ||
+ | <ul> | ||
+ | <li>Restart amilCP cloning process</li> | ||
+ | </ul> | ||
+ | <h3>Cell-Free Extract</h3> | ||
+ | <ul> | ||
+ | <li>Linear eGFP construct does not produce a stronger signal than its plasmid form</li> | ||
+ | </ul> | ||
+ | <h3>DNAzyme</h3> | ||
+ | <ul> | ||
+ | <li>DNAzyme duplex does not trigger toehold switch</li> | ||
+ | <li>Erbium cleaves the P substrate strand</li> | ||
+ | </ul> | ||
+ | <h2>Dry Lab</h2> | ||
+ | <ul> | ||
+ | <li>First presentation at Camp BioE</li> | ||
+ | <li>Prepare for UMD Jamboree</li> | ||
+ | <li>Contact PLSG and NEB for sponsorship</li> | ||
+ | </ul> | ||
+ | <a href="" target="_blank">Week 8 Notebook</a><br> | ||
<a href="#Top">Back to Top</a> | <a href="#Top">Back to Top</a> | ||
Revision as of 16:34, 15 July 2016
Contact Us
Our weekly progress. For a list of our protocols, visit the Protocols page
Week 1: May 23 - May 27
Wet Lab
- Training begins
- Grow Top 10 competent cells.
Dry Lab
- Brainstorm genetic circuits for a thallium sensor
- Lab safety training
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Week 2: May 31 - June 3
Wet Lab
- Test efficiency of competent cells
Cell-Free Extract
- Test cell-free extract reaction with T7-GFP plasmid
Dry Lab
- Contact museums and summer programs for outreach opportunities
- Lab safety training
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Week 3: June 6 - June 12
Wet Lab
Reporter
- Transform T7 promoter, amilCP, and terminator
- Begin assembly by ligating linearized T7 promoter and amilCP
Dry Lab
- Contact museums and summer programs for outreach opportunities
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Week 4: June 13 - June 17
Wet Lab
Reporter
- Transform T7-GFP plasmid, lacZ alpha fragment, and eGFP
- Send promising T7 promoter -- amilCP ligations to be sequenced
- Perform double digest of T7 promoter and terminator from last week
- Ligate double-digested T7 promoter to new reporters (lacZ and eGFP)
Dry Lab
- TECBio, DiSCoBio, and Tissue Engineering Camp outreach opportunities set
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Week 5: June 20 - June 26
Wet Lab
Reporter
- Ligate T7 promoter -- amilCP construct to terminator
- Extract successful ligations of T7 promoter to eGFP
- Ligate T7 promoter -- eGFP construct to terminator
Cell-Free Extract
- Reaction volume can be reduced to 5 μL with 5 ng/μL of DNA
Toehold Switch
- Collins triggers activate the switches (both in plasmid form) to express LacZ
Dry Lab
- Reach out to teams to collaborate based on last year's projects
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Week 6: June 27 - July 3
Wet Lab
Reporter
- Identify successful ligations to terminator for amilCP and eGFP consturcts using a gel
- Send correct plasmids for sequencing for confirmation
- Test plasmids in cell-free extract
- amilCP does not produce color in cell-free reaction
- eGFP produces fluorescence comparable to that from the Collins T7-GFP plasmid in cell-free reaction
- Linearized plasmids containing only the promoter and insert (no terminator) do not express protein
Cell-Free Extract
- Reaction volume can be reduced to 1 μL with 5 ng/μL of DNA
Toehold Switch
- Collins plasmids express LacZ with 25 ng of switch
- DNA oligos trigger Collins switches
Dry Lab
- Work on outreach presentation for tissue engineering camp
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Week 7: July 5 - July 8
Wet Lab
Reporter
- Sequenced amilCP construct does not contain amilCP
- Unsuccessfully linearize and amplify eGFP construct using PCR
Cell-Free Extract
- 384-well plate requires at least 10 μL of reaction
DNAzyme
- Anneal PO strand with catalytic strand, both with and without erbium
- Test success of annealing reaction in cell-free extract and with acrylamide gels
Dry Lab
- Practice outreach presentation for tissue engineering camp
- Develop DNAzymes for other heavy metals
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Week 8: July 11 - July 17
Wet Lab
Reporter
- Restart amilCP cloning process
Cell-Free Extract
- Linear eGFP construct does not produce a stronger signal than its plasmid form
DNAzyme
- DNAzyme duplex does not trigger toehold switch
- Erbium cleaves the P substrate strand
Dry Lab
- First presentation at Camp BioE
- Prepare for UMD Jamboree
- Contact PLSG and NEB for sponsorship
Back to Top