Difference between revisions of "Team:Lethbridge HS/Attributions"
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jQuery(document).ready(function() { | jQuery(document).ready(function() { | ||
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function makeBiofilms(){ | function makeBiofilms(){ | ||
+ | jQuery(".biofilms").show(); | ||
+ | jQuery(".bees").hide(); | ||
+ | jQuery(".active").addClass("biofilmsActive"); | ||
+ | |||
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jQuery("#mainTitleText").text('Biofilms!!!'); | jQuery("#mainTitleText").text('Biofilms!!!'); | ||
jQuery("#coloredTitle").text('Biofilms'); | jQuery("#coloredTitle").text('Biofilms'); | ||
jQuery("#slide1Title").text('Biofilm'); | jQuery("#slide1Title").text('Biofilm'); | ||
+ | document.getElementById("projectText1").write('The purpose of hospitals is to help people get better. However, in the United States, 2 million people are infected during their hospital stay and bacterial biofilms are responsible of 65% of all hospital acquired infections. A biofilm is a conglomeration of bacteria that is enclosed in a matrix of sugars and extracellular DNA, this helps to hold the bacteria together like'); | ||
jQuery("#slide1Paragraph").text('For years, bacterial biofilms have been a cause for concern in medicine. Biofilms are comprised of colonial microorganisms that can adhere to almost any surface with adequate moisture and nutrients. Biofilms often harbour pathogens, and can be extremely problematic in clinical settings. 65% of all hospital acquired infections can be attributed to pathogenic biofilms. Current methods to destroy biofilms include antimicrobial agents and hydraulic flushing. These are ineffective because biofilms are surrounded by a matrix of sugars and DNA. We intend to create an all-purpose biological counterattack capable of dispersing and eliminating a wide variety of biofilms by utilizing enzymes to destroy the structures within. This will be achieved through the secretion of dextranase, which degrades the exopolymeric matrix, and DNase, that targets the extracellular DNA responsible for maintaining biofilm structure. This double phased attack will be highly efficient compared to current removal methods.'); | jQuery("#slide1Paragraph").text('For years, bacterial biofilms have been a cause for concern in medicine. Biofilms are comprised of colonial microorganisms that can adhere to almost any surface with adequate moisture and nutrients. Biofilms often harbour pathogens, and can be extremely problematic in clinical settings. 65% of all hospital acquired infections can be attributed to pathogenic biofilms. Current methods to destroy biofilms include antimicrobial agents and hydraulic flushing. These are ineffective because biofilms are surrounded by a matrix of sugars and DNA. We intend to create an all-purpose biological counterattack capable of dispersing and eliminating a wide variety of biofilms by utilizing enzymes to destroy the structures within. This will be achieved through the secretion of dextranase, which degrades the exopolymeric matrix, and DNase, that targets the extracellular DNA responsible for maintaining biofilm structure. This double phased attack will be highly efficient compared to current removal methods.'); | ||
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} | } | ||
function makeBees(){ | function makeBees(){ | ||
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− | jQuery("#coloredTitle").text(' | + | jQuery("#coloredTitle").text('Varroa'); |
− | jQuery("#slide1Title").text(' | + | jQuery("#slide1Title").text('Introduction'); |
jQuery("#slide1Paragraph").text('The top 100 food crops produced provide 90% of the world’s nutrition. 70% of these crops are pollinated by bees. A phenomenon called Colony Collapse Disorder (CCD) has decimated honeybee colonies across the world, halving the number of productive colonies worldwide. One of the main factors hypothesized to contribute to CCD is the mite and viral vector Varroa destructor. While feeding on the bee’s hemolymph, Varroa destructor expels RNA viruses into the bee crippling colony’s strength. Current commercial methods to eradicate Varroa have seen a gradual development of resistance in treated populations. Using synthetic biology, we plan to target Varroa more effectively by directly delivering the miticide, oxalic acid into Varroa and utilizing RNA interference to eliminate Varroa populations within commercial hives.'); | jQuery("#slide1Paragraph").text('The top 100 food crops produced provide 90% of the world’s nutrition. 70% of these crops are pollinated by bees. A phenomenon called Colony Collapse Disorder (CCD) has decimated honeybee colonies across the world, halving the number of productive colonies worldwide. One of the main factors hypothesized to contribute to CCD is the mite and viral vector Varroa destructor. While feeding on the bee’s hemolymph, Varroa destructor expels RNA viruses into the bee crippling colony’s strength. Current commercial methods to eradicate Varroa have seen a gradual development of resistance in treated populations. Using synthetic biology, we plan to target Varroa more effectively by directly delivering the miticide, oxalic acid into Varroa and utilizing RNA interference to eliminate Varroa populations within commercial hives.'); | ||
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} | } | ||
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− | <a href=" | + | <a href="https://2015.igem.org/Team:Lethbridge_HS/Description">Background</a> |
− | <a href=" | + | <a href="https://2015.igem.org/Team:Lethbridge_HS/Experiments">Experiments</a> |
+ | <a href="https://2015.igem.org/Team:Lethbridge_HS/Results">Results</a> | ||
+ | <a href="https://2015.igem.org/Team:Lethbridge_HS/Parts">Parts</a> | ||
+ | <a href="https://2015.igem.org/Team:Lethbridge_HS/Achievements">Achievements</a> | ||
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− | <li ><a href=" | + | <li margin-top:2%; style="margin-top:2%;"><a class="textItem" href="https://2015.igem.org/Team:Lethbridge_HS/Notebook">Notebook</a></li> |
− | <li><a href=" | + | <li margin-top:2%; style="margin-top:2%;"><a class="textItem" href="https://2015.igem.org/Team:Lethbridge_HS/Safety">Safety</a></li> |
− | + | <li class= "dropdown texItem" style="margin-top:2%;"> | |
− | + | <a class="textItem" href="https://2015.igem.org/Team:Lethbridge_HS/Team" class="dropdown-toggle" data-toggle = "dropdown">Team<b class="caret"></b></a> | |
+ | <ul class="dropdown-menu"> | ||
+ | <li> | ||
+ | <a href="https://2015.igem.org/Team:Lethbridge_HS/Team">Students</a> | ||
+ | <a href="https://2015.igem.org/Team:Lethbridge_HS/Team#section2">Advisors</a> | ||
+ | <a class="texItem" href="https://2015.igem.org/Team:Lethbridge_HS/Team#section3">Sponsors</a> | ||
+ | <a class="texItem" href="https://2015.igem.org/Team:Lethbridge_HS/Attributions">Attributions</a> | ||
+ | <a class="texItem" href="https://2015.igem.org/Team:Lethbridge_HS/Collaborations">Collaborations</a> | ||
+ | </li> | ||
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− | <p id="pageTitleText"> | + | <div style="z-index:2;" class="pageIcon flaticon-business53"></div> |
− | + | <p id="pageTitleText">Team<br></p><p id="pageSubtitleText"><span>Collaborations</span></p> | |
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− | <li><a href="#section1"> | + | <li><a href="#section1"><h2>Description</h2></a></li> |
− | + | <li class="biofilms"><a href="#section1"><p>What is nuclease? What is dextranase?</p></a></li> | |
− | + | <li class="biofilms"><a href="#section1"><p>What we are doing differently</p></a></li> | |
− | + | <li class="biofilms"><a href="#section1"><p>Extracellular Polymeric Substance Matrix</p></a></li> | |
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− | + | <section id="section1"> | |
− | + | <h1 id="projecttext1" class="contentSubTitle">Attributions<br><small></small></h1> | |
+ | <p>We thank:<br><br> | ||
+ | Sydnee Calhoun, Tiffany Dang, Dinula De Silva, Ronja Kothe, Jonathan Kwan, Anileen Pageni, and Aum Patel for conducting lab experiments. <br><br> | ||
+ | Eyram Asem, Sydnee Calhoun, Dinula De Silva, Marissa King, Ronja Kothe, Anileen Pageni, Kaatje O’Donnell, Ross Oliver, Jessica Semmelrock, Sunny Sun, and David Zhang for contributing their time to human practices .<br><br> | ||
+ | Tiffany Dang for helping raise funds to support our project endeavors.<br><br> | ||
+ | Dinula De Silva, Marissa King, and Jonathan Kwan for their work on the wiki.<br><br> | ||
+ | University of Lethbridge, Chemistry and Biochemistry Department for hosting the wet lab workspace as well as the classrooms for our weekly meetings. <br><br> | ||
+ | Wieden and Kothe lab for providing wet lab equipment and reagents needed in day-to-day experiments.<br><br> | ||
+ | Dr. Hans-Joachim Wieden for hosting the iGEM program and overseeing administrative matters.<br><br> | ||
+ | Dr. Brian Dempsey for mentoring the team in day-to-day affairs, planning and organizing high school workshops, and handling administrative matters. <br><br> | ||
+ | Advisor Kieran McCormack for hosting wet lab times and executing biofilm related experiments.<br><br> | ||
+ | Advisor Chris Isaac for hosting wet lab times and executing bee related experiments. <br><br> | ||
+ | Advisor Yoyo Yao for helping in construct building and getting team T-shirts<br><br> | ||
+ | Joe Mauro for guiding us in the direction of how we would approach changing a bylaw. <br><br> | ||
+ | Shannon Phillips for sitting down with us for an interview on her thoughts about our Bee/Biofilms project. <br><br> | ||
+ | Ryan Carriere for letting us interview him to discuss our urban planning ideas for Lethbridge.<br><br> | ||
+ | Audrey and Ron King for their kind donation towards our Boston travel fees.<br><br> | ||
+ | Lethbridge School District 51 for allowing us to present in their classrooms and provide us with outreach opportunities for fellow high schoolers. <br><br> | ||
+ | Dr. John Hasell, Plastic and Reconstructive surgeon, for giving us his time in answering some questions in regards to how our biofilms project can be implemented in the real world. <br><br> | ||
+ | The beekeepers who showed us their beehives, their time, and provided valuable insight into beekeeping. <br><br> | ||
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Latest revision as of 01:51, 19 September 2015
Team
Collaborations
Attributions
We thank:
Sydnee Calhoun, Tiffany Dang, Dinula De Silva, Ronja Kothe, Jonathan Kwan, Anileen Pageni, and Aum Patel for conducting lab experiments.
Eyram Asem, Sydnee Calhoun, Dinula De Silva, Marissa King, Ronja Kothe, Anileen Pageni, Kaatje O’Donnell, Ross Oliver, Jessica Semmelrock, Sunny Sun, and David Zhang for contributing their time to human practices .
Tiffany Dang for helping raise funds to support our project endeavors.
Dinula De Silva, Marissa King, and Jonathan Kwan for their work on the wiki.
University of Lethbridge, Chemistry and Biochemistry Department for hosting the wet lab workspace as well as the classrooms for our weekly meetings.
Wieden and Kothe lab for providing wet lab equipment and reagents needed in day-to-day experiments.
Dr. Hans-Joachim Wieden for hosting the iGEM program and overseeing administrative matters.
Dr. Brian Dempsey for mentoring the team in day-to-day affairs, planning and organizing high school workshops, and handling administrative matters.
Advisor Kieran McCormack for hosting wet lab times and executing biofilm related experiments.
Advisor Chris Isaac for hosting wet lab times and executing bee related experiments.
Advisor Yoyo Yao for helping in construct building and getting team T-shirts
Joe Mauro for guiding us in the direction of how we would approach changing a bylaw.
Shannon Phillips for sitting down with us for an interview on her thoughts about our Bee/Biofilms project.
Ryan Carriere for letting us interview him to discuss our urban planning ideas for Lethbridge.
Audrey and Ron King for their kind donation towards our Boston travel fees.
Lethbridge School District 51 for allowing us to present in their classrooms and provide us with outreach opportunities for fellow high schoolers.
Dr. John Hasell, Plastic and Reconstructive surgeon, for giving us his time in answering some questions in regards to how our biofilms project can be implemented in the real world.
The beekeepers who showed us their beehives, their time, and provided valuable insight into beekeeping.