Team:Penn State/Notebook
From 2014.igem.org
Line 134: | Line 134: | ||
<p><h4><a name="Week 1"><font color="black">Week 1 </font></a><br> Tuesday, May 20 - Sunday, May 25</h4> <h5>- <a href="#NB wk1">Notebook Entries</a></h5> </p> | <p><h4><a name="Week 1"><font color="black">Week 1 </font></a><br> Tuesday, May 20 - Sunday, May 25</h4> <h5>- <a href="#NB wk1">Notebook Entries</a></h5> </p> | ||
<p>iGEM 2014 had their first meeting with Dr. Salis and Dr. Richard. Ashlee, Emily, Clay, and Sam met each other. Emily will help Ashlee continue work on her Honors Thesis with the project <a href="https://2014.igem.org/Team:Penn_State/Biodetoxification">"Engineering a Biodetoxification Pathway for Lignocellulosic Feedstock"</a>. Ashlee began to show Emily around the lab and instruct her during her first cloning experiences while they continued Ashlee's semester research trying to add a terminator upstream of the HMF pathway where dCas9 would be inserted. The dCas9 system has a transacting RNA sequence which could disrupt upstream genes if it was not turned off correctly.</p> | <p>iGEM 2014 had their first meeting with Dr. Salis and Dr. Richard. Ashlee, Emily, Clay, and Sam met each other. Emily will help Ashlee continue work on her Honors Thesis with the project <a href="https://2014.igem.org/Team:Penn_State/Biodetoxification">"Engineering a Biodetoxification Pathway for Lignocellulosic Feedstock"</a>. Ashlee began to show Emily around the lab and instruct her during her first cloning experiences while they continued Ashlee's semester research trying to add a terminator upstream of the HMF pathway where dCas9 would be inserted. The dCas9 system has a transacting RNA sequence which could disrupt upstream genes if it was not turned off correctly.</p> | ||
- | <p><font color=" | + | <p><font color="black">Clay and Sam began work for Clay's Honors Thesis in Biological Engineering on the <a href="https://2014.igem.org/Team:Penn_State/CodonOptimization">"Codon Optimization"</a> project. Clay and Sam began preliminary research and worked on constructing a program to optimize GFPs.</font></p> |
<p><h4><a name="Week 2"><font color="black">Week 2</font></a><br>Monday, May 26 - Sunday, June 1</h4><h5>- <a href="#NB wk2">Notebook Entries</a></h5></p> | <p><h4><a name="Week 2"><font color="black">Week 2</font></a><br>Monday, May 26 - Sunday, June 1</h4><h5>- <a href="#NB wk2">Notebook Entries</a></h5></p> | ||
Line 142: | Line 142: | ||
<p><h4><a name="Week 3"><font color="black">Week 3</font></a><br>Monday, June 2 - Sunday, June 8</h4><h5>- <a href="#NB wk3">Notebook Entries</a></h5></p> | <p><h4><a name="Week 3"><font color="black">Week 3</font></a><br>Monday, June 2 - Sunday, June 8</h4><h5>- <a href="#NB wk3">Notebook Entries</a></h5></p> | ||
- | <p></p> | + | <p>Decisions made to use restriction site cloning to introduce synthetic GFPs into pFTV. Also, determined that best method of obtaining the genes is ordering them as gblocks from IDT. Problem of RBS library anticipated, synthetic leader sequence developed in order to work around the problem of the coding sequences being different. </p> |
<p><h4><a name="Week 4"><font color="black">Week 4</font></a><br>Monday, June 9 - Sunday, June 15</h4><h5>- <a href="#NB wk4">Notebook Entries</a></h5></p> | <p><h4><a name="Week 4"><font color="black">Week 4</font></a><br>Monday, June 9 - Sunday, June 15</h4><h5>- <a href="#NB wk4">Notebook Entries</a></h5></p> | ||
- | <p></p> | + | <p>Project Plan updated extensively as mistake in design of gblocks realized (truncation) as well as the addition of a fifth gblock (slow insertion time). Programs written to optimize for insertion time as well as total the insertion time for existing genes. Restriction enzymes re-chosen and gblocks ordered. Project plan modified to include a gene first, RBS later strategy.</p> |
<p><h4><a name="Week 5"><font color="black">Week 5</font></a><br>Monday, June 16 - Sunday, June 22</h4><h5>- <a href="#NB wk5">Notebook Entries</a></h5></p> | <p><h4><a name="Week 5"><font color="black">Week 5</font></a><br>Monday, June 16 - Sunday, June 22</h4><h5>- <a href="#NB wk5">Notebook Entries</a></h5></p> | ||
- | <p></p> | + | <p>Gblocks amplified with rescue PCR, digested along with pFTV, ligated and transformed into cells. Additional design steps taken toward finding suitable RBS library. Began to work on website and other iGEM forms.</p> |
<p><h4><a name="Week 6"><font color="black">Week 6</font></a><br>Monday, June 23 - Sunday, June 29</h4><h5>- <a href="#NB wk6">Notebook Entries</a></h5></p> | <p><h4><a name="Week 6"><font color="black">Week 6</font></a><br>Monday, June 23 - Sunday, June 29</h4><h5>- <a href="#NB wk6">Notebook Entries</a></h5></p> | ||
- | <p></p> | + | <p>Colonies sent for sequencing, discovered that no insert was present. Decision reached to attempt digestion, ligation, transformation again.</p> |
<p><h4><a name="Week 7"><font color="black">Week 7</font></a><br>Monday, June 30 - Sunday, July 6</h4><h5>- <a href="#NB wk7">Notebook Entries</a></h5></p> | <p><h4><a name="Week 7"><font color="black">Week 7</font></a><br>Monday, June 30 - Sunday, July 6</h4><h5>- <a href="#NB wk7">Notebook Entries</a></h5></p> | ||
- | <p></p> | + | <p>Problems realized with inverse PCR. Several attempts made to optimize this reaction. Success near end of week as strong bands observed. These will be used in the next digestion, ect. Digestion, ligation, transformation carried out again, cells plated. No colonies observed.</p> |
<p><h4><a name="Week 8"><font color="black">Week 8</font></a><br>Monday, July 7 - Sunday, July 13</h4><h5>- <a href="#NB wk8">Notebook Entries</a></h5></p> | <p><h4><a name="Week 8"><font color="black">Week 8</font></a><br>Monday, July 7 - Sunday, July 13</h4><h5>- <a href="#NB wk8">Notebook Entries</a></h5></p> | ||
- | <p></p> | + | <p>Standard enzymatic digestion, ligation, attempted one more time, with sufficient optimization from the last two attempts. Used Chiam's electrocompetent cells, as it is suspected that ours are bad. Colonies observed, DNA harvested, digested to see if expected bands observed, sent for sequencing. </p> |
<p><h4><a name="Week 9"><font color="black">Week 9</font></a><br>Monday, July 14 - Sunday, July 20</h4><h5>- <a href="#NB wk9">Notebook Entries</a></h5></p> | <p><h4><a name="Week 9"><font color="black">Week 9</font></a><br>Monday, July 14 - Sunday, July 20</h4><h5>- <a href="#NB wk9">Notebook Entries</a></h5></p> | ||
- | <p></p> | + | <p>Sequencing results show presence of an insert, but also include significant regions of ambiguity. Attemps made to send for sequencing on campus. Numerous improvements made to plasmid harvest protocol. Improvements made to website and journal. Skills gained in html, CSS coding.</p> |
<p><h4><a name="Week 10"><font color="black">Week 10</font></a><br>Monday, July 21 - Sunday, July 27</h4><h5>- <a href="#NB wk10">Notebook Entries</a></h5></p> | <p><h4><a name="Week 10"><font color="black">Week 10</font></a><br>Monday, July 21 - Sunday, July 27</h4><h5>- <a href="#NB wk10">Notebook Entries</a></h5></p> |
Revision as of 22:48, 10 July 2014
WELCOME TO PENN STATE iGEM 2014!(Page under construction) |
|||||||||||||
| |||||||||||||
Penn State iGEM 2014 Notebook PageHere you will find weekly summaries of our wet laboratory progress, team updates, and accomplishments outside the laboratory. Follow this link to our detailed, day-to-day Laboratory Notebook. Weekly SummariesWeek 1 |