Team:Tsinghua

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Welcome to iGEM08 Tsinghua's wiki page


Contents

Intro of Our Project

Tsinghua University was established in 1911, originally under the name “Tsinghua Xuetang”. The school was renamed "Tsinghua School" in 1912. The university section was founded in 1925. The name “National Tsinghua University” was adopted in 1928.click here to see more pictures

The educational philosophy of Tsinghua is to "train students with integrity." Among over 120,000 students who have graduated from Tsinghua since its founding are many outstanding scholars, eminent entrepreneurs and great statesmen remembered and respected by their fellow Chinese citizens.

With the motto of “Self-Discipline and Social Commitment” and the spirit of “Actions Speak Louder than Words”, Tsinghua University is dedicated to the well-being of Chinese society and to world development.

Thu Logo.jpg

News

GF taq is recommended in our PCR reactions. 2008.June.25

The first plasmid is successfully constrcuted. 2008.Jul.20

The gene we need is at synthesis in Geneart. 2008.Jul.24

The standard vector pSB1A3 lost in the transformation. 2008.Jul.28

Then it finally succeeds. 2008.Jul.31

Template of one of the receptors are still in vacancy.

New edition of project interpretation are in process.

Intro of Tsinghua University

Tsinghua University was established in 1911, originally under the name “Tsinghua Xuetang”. The school was renamed "Tsinghua School" in 1912. The university section was founded in 1925. The name “National Tsinghua University” was adopted in 1928.click here to see more pictures

The educational philosophy of Tsinghua is to "train students with integrity." Among over 120,000 students who have graduated from Tsinghua since its founding are many outstanding scholars, eminent entrepreneurs and great statesmen remembered and respected by their fellow Chinese citizens.

With the motto of “Self-Discipline and Social Commitment” and the spirit of “Actions Speak Louder than Words”, Tsinghua University is dedicated to the well-being of Chinese society and to world development.

Thu 1.jpg

== Our Schedule ==

  Time	                      Events
Dec. 15, 2007	              Team of Tsinghua University Founded
Dec. 31, 2007	              Brain Storm(1)
Jan-Feb, 2008	              Backgroud Investigation
Feb.25, 2008	              Brain Storm(2)
Mar., 2008	              Experimental procedure design;
                             Modeling in silico Started  
Apr.1,2008	              Wet Lab work started
Apr.-Aug.,2008	              Wet Lab Work
May.1, 2008	              Team Registry
May.25, 2008	              Students’ Association of Synthetic Biology(SASB) Founded
June.21, 2008	              “Teach the teacher “workshop, in Kyoto, Japan
Sept.-Oct., 2008	      Inspection and Revision     
Oct.20,2008	              Summary, Presentation Preparation
Nov.8-9,2008	              Jamboree In MIT

Molecular cloning

  1   PCR
    
 1.1 Gold Faster 	Taq system:
   Reagent	           Concentration/Activity	50ul 	100ul
   GF taq buffer     	    10x	                         5       10
   GF taq		                                 0.5	  0.5
   dNTPmix	            10mM each	                 1	  2
   Primer 1 	            10uM	                 1	  2
   Primer 2	            10um	                 1	  2
   Template DNA	      changeable	                 0.5	  1
   MgCl2	            0.2M	                 0.5	  1
   ddH2O	                ---	                40.5	 81
 1.2 The program under Gold faster taq system
   Progress	     Program I	                 Program 2
   Predenaturing    95℃         2-5 min	         95℃   2-5 min
   Denaturing	     95℃        10-20sec	         95℃   10-20sec
   Annealing	     (Tm-5) ℃   2-5 sec	         68℃   10-15sec/1kb
   Extension	     72℃        10-15sec/1kb	

25-30cycle 25-30cycle

   Last extension	  1-2min or skipped	       1-2min or skipped
   2 	Restriction cut:
           Reagent	        Concentration/Activity	 Volume(50ul system)
           Restriction cut buffer	10x	           5ul
           Enzyme 1	                --	           2.5ul
           Enzyme 2	                --	           2.5ul
 Incubate at 37℃, 1.5 hrs or longer
 (Enzymes from Takara Co., Ltd)
     3  Ligation:
              Reagent	    Volume(10ul system)
              Solution I	5ul
              DNA fragment	3.5ul
              Vector	        1.5ul
   Incubate at 16-18℃,1hr or longer
   (Ligation kit from Takara)


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