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> Igem-Taiwan </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">IGem-Taiwan Yeastherm</h1>
+
             <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 with Thermogenic Yeast<br/>
+
                 Working on Thermogenic Yeast<br/>
-
                 Apps with knowledge of iGEM competition and synthetic biology.
+
                 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/>
+
         <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>
+
<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

iGEM-NTU-Taiwan