"
Team:NTU Taiwan/index.html
From 2013.igem.org
(Difference between revisions)
| (2 intermediate revisions not shown) | |||
| Line 1: | Line 1: | ||
<html lang="en"> | <html lang="en"> | ||
<head> | <head> | ||
| - | <title> | + | <title> iGEM-NTU-Taiwan </title> |
<meta name="viewport" content="width=device-width, initial-scale=1.0"> | <meta name="viewport" content="width=device-width, initial-scale=1.0"> | ||
<meta http-equiv="X-UA-Compatible" content="IE=edge"> | <meta http-equiv="X-UA-Compatible" content="IE=edge"> | ||
| Line 199: | Line 199: | ||
<span class="particle particle--b"></span> | <span class="particle particle--b"></span> | ||
</div> | </div> | ||
| - | <h1 class=" rainbow-text header"> | + | <h1 class=" rainbow-text header">iGEM-NTU-Taiwan YeasTherm</h1> |
<p class="header container"> | <p class="header container"> | ||
<img class="spin" alt-src="images/LaboratoryLevels.png" src="/wiki/images/9/91/NTU_TAIWAN_LaboratoryLevels.png"><br/> | <img class="spin" alt-src="images/LaboratoryLevels.png" src="/wiki/images/9/91/NTU_TAIWAN_LaboratoryLevels.png"><br/> | ||
National Taiwan University<br/> | National Taiwan University<br/> | ||
| - | Working | + | Working on Thermogenic Yeast<br/> |
| - | Apps with | + | Apps with concept of iGEM competition and synthetic biology. |
</p> | </p> | ||
</section> | </section> | ||
| Line 2,162: | Line 2,162: | ||
<div class="container"> | <div class="container"> | ||
| - | <br/><p><b>PCR</b></p | + | <br/><p><b>PCR</b></p> |
1: Design of appropriate forward and reverse primers<br/> | 1: Design of appropriate forward and reverse primers<br/> | ||
2: Prepare our template<br/> | 2: Prepare our template<br/> | ||
| Line 2,168: | Line 2,168: | ||
4: Run PCR<br/> | 4: Run PCR<br/> | ||
5: Examine the results by electrophoresis<br/> | 5: Examine the results by electrophoresis<br/> | ||
| - | Note: If the template is genomic DNA, we would adjust the annealing temperature at 45°C. It is because the copy number of target gene may be low. We use this annealing temp when perform PCR of Tir1, 26s, 5.8s ITS | + | Note: If the template is genomic DNA, we would adjust the annealing temperature at 45°C. It is because the copy number of target gene may be low. We use this annealing temp when perform PCR of Tir1, 26s, 5.8s ITS<br/><br/> |
| - | <br/><p><b>Construction of our parts</b></p | + | <br/><p><b>Construction of our parts</b></p><p> |
1: We design primers for parts with prefix and suffix.<br/> | 1: We design primers for parts with prefix and suffix.<br/> | ||
2: Perform PCR and cleanup the PCR product<br/> | 2: Perform PCR and cleanup the PCR product<br/> | ||
Latest revision as of 04:22, 28 September 2013
