Team:WHU-China/calendarjs

From 2011.igem.org

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}, { id: 999, title: 'Transform pDsRed-Express Vector plasmid(2)', start: new Date(y, m-1, 26),

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}, { id: 999, title: 'Vocation', start: new Date(y, m, 1), end: new Date(y,m,10) }, { title: 'Use enzyme SpelⅠto digest pDsRed-Express Vector plasmid', start: new Date(y,m,12),

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}, { title: 'XbalⅠin digesting', start: new Date(y, m, 27)


}, { title: 'EcoRⅠin digesting', start: new Date(y, m, 28)

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},

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title: 'Produce the competent cell', start: new Date(y, m+1, 2), end: new Date(y, m+1, 15)

}, { title: 'Pick up the procedures of transformation after the break', start: new Date(y, m+2, 8), end: new Date(y, m+2, 9)

}, { title: 'Transform the products of ligation', start: new Date(y, m+2, 10)


}, { title: 'Tranform the plasmid of pSB1A3...', start: new Date(y, m+2,11 )

}, { title: 'Re-transform pSB1C3, biobricks 15NI...', start: new Date(y, m+2,12 )


}, { title: 'Extract the plasmid of 15NI,6AI', start: new Date(y, m+2, 13)


}, { title: 'Re-transform the pSB1A3 and the biobricks...', start: new Date(y, m+2, 14)


}, { title: 'Transformed Single biobricks(1)', start: new Date(y, m+2, 15), end: new Date(y, m+2, 17)

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                                ,

{ title: 'Transformed Single biobricks(2)', start: new Date(y, m+2,18 )


}, { title: 'Transformed Single biobricks(3)', start: new Date(y, m+2, 19), end: new Date(y, m+1, 1)

}, { title: 'Transformed Single biobricks(4)', start: new Date(y, m+2, 20)


}

                                ,

{ title: 'The second layer assembly(1)', start: new Date(y,m+2,21)


}, { title: 'The second layer assembly(2)', start: new Date(y,m+2,22)


}, { title: 'The second layer assembly(3)', start: new Date(y,m+2,23),

                                       end: new Date(y,m+2,28)

}, { title: 'The second layer assembly(4)', start: new Date(y,m+2,29)


}, { title: 'The third layer assembly(1)', start: new Date(y,m+2,30)


}, { title: 'The third layer assembly(2)', start: new Date(y,m+2,31)


}, { title: 'The third layer assembly(3)', start: new Date(y,m+3,1),

                                       end: new Date(y,m+3,2)

}, { title: 'The third layer assembly(4)', start: new Date(y,m+3,3)

}

                                ,
                               {

title: 'Re-ligate the failure products(1)', start: new Date(y,m+3,4),

                                       end: new Date(y,m+3,6)

}, { title: 'Re-ligate the failure products(2)', start: new Date(y,m+3,7), end: new Date(y,m+3,12) }, { title: 'Re-ligate the failure products(3)', start: new Date(y,m+3,13),

                                       end: new Date(y,m+3,15)

}, { title: 'Re-ligate the failure products(4)', start: new Date(y,m+3,16), end: new Date(y,m+3,18) }, { title: 'Re-ligate the failure products(5)', start: new Date(y,m+3,19), end: new Date(y,m+3,22) }, { title: 'Re-ligate the failure products(6)', start: new Date(y,m+3,23), end: new Date(y,m+3,25) }, { title: 'Jamboree', start: new Date(y, m+5, 15)


}, { title: 'World Final', start: new Date(y, m+6, 5)


},{ title: 'Extract plasmid: 009-13,009-3', start: new Date(y, m+3, 26)


},

                                {

title: 'Extract plasmid: 8H, 2M-14 H-2M', start: new Date(y, m+3, 27)


},

                                {

title: 'Repeat 27th enzymes digest', start: new Date(y, m+3, 28)

},

                                {

title: 'PCR 2 M-19 C, Enzyme cut...', start: new Date(y, m+3, 29)


},

                                {

title: 'Extract plasmid 18 O I...', start: new Date(y, m+3, 30)


},

                                {

title: 'PCR screening 18 O-RLS...', start: new Date(y, m+3, 31)


},

                                {

title: 'Extract plasmid 18 O, 18 M- RLS...', start: new Date(y, m+4, 1)


}

                                ,
                                {

title: 'Green light sensor assembly', start: new Date(y, m+4, 2), end:new Date(y,m+4,3)

},

                                {

title: 'Reporting system assembly(1)', start: new Date(y, m+4, 4), end:new Date(y,m+4,5)

},

                                {

title: 'Reporting system assembly(2)', start: new Date(y, m+4, 6), end:new Date(y,m+4,7)

},

                                {

title: 'Reporting system assembly(3)', start: new Date(y, m+4, 8), end:new Date(y,m+4,9)

},

                                {

title: 'Reporting system assembly(4)', start: new Date(y, m+4, 10), end:new Date(y,m+4,11)

},{ title: 'Reporting system assembly(5)', start: new Date(y, m+4, 12), end:new Date(y,m+4,13)

},{ title: 'The fifth layer assembly(1)', start: new Date(y, m+4, 14)


},{ title: 'The fifth layer assembly(2)', start: new Date(y, m+4, 15)


},{ title: 'The fifth layer assembly(3)', start: new Date(y, m+4, 16)


},{ title: 'Second step of green light sensor assemble(1)', start: new Date(y, m+4, 17), end: new Date(y,m+4,19)

},{ title: 'Second step of green light sensor assemble(2)', start: new Date(y, m+4, 20), end: new Date(y,m+4,22)

},{ title: 'Blue light sensor assembly(1)', start: new Date(y, m+4, 23), end:new Date(y,m+4,26)

},{ title: 'Blue light sensor assembly(2)', start: new Date(y, m+4, 27), end:new Date(y,m+4,29)

}



], eventClick: function(calEvent, jsEvent, view) {

                            var resultview=calEvent.title;
                            var e11={x:"Preparing Materials",y:"4/14~4/15, preparing materials: such as DH5α, pDsRed -Express Vector, amp, kana, TB, 0.85%NaCl, 0.1MCaCl2, 0.1MMg2+"};
                           var e12={x:"Transform pDsRed-Express Vector plasmid(1)",y:"4/24, successfully obtained pDsRed-Express Vector plasmid"};

var e13={x:"Transform pDsRed-Express Vector plasmid(2)",y:"4/26~4/29, transform pDsRed-Express Vector plasmid into DH5αcompetent cell in order to test our experiment skills"}; var e14={x:"Vocation",y:"5/1~5/10, vocation"}; var e21={x:"Use enzyme SpelⅠto digest pDsRed-Express Vector plasmid",y:"5/11~5/26, use enzyme SpelⅠto digest pDsRed-Express Vector plasmid"}; var e22={x:"XbalⅠin digesting",y:"5/27, use XbalⅠto digest pDsRed-Express Vector plasmid"}; var e23={x:"EcoRⅠin digesting",y:"5/28, use EcoRⅠto digrst pDsRed-Express Vector plasmid"}; var e24={x:"Use Pst1 and EcoRⅠto digest pDsRed-Express Vector",y:"5/29~6/1, use Pst1 and EcoRⅠto digest pDsRed-Express Vector"}; var e25={x:"Produce the competent cell",y:" 6/2~6/15, produce the competent cell, use T4 ligase to join DNA fragments, and conduct the transformation..During those days, we modified the procedures of competent cell production and successfully boomed the results of transformation to 10^7"}; var e31={x:"Pick up the procedures of transformation after the break",y:"7/8~7/9, pick up the procedures of transformation after the break. At the meantime, use PstI and EcoRI to digest the pDsRed-Express Vector, conduct the gel extraction and join the DNA fragments overnight"}; var e32={x:"Transform the products of ligation",y:"7/10, transform the products of ligation"}; var e33={x:"Tranform the plasmid of pSB1A3...",y:"7/11, tranform the plasmid of pSB1A3, pSB1C3 and biobrick 15NI, 6AI"}; var e34={x:"Re-transform pSB1C3, biobricks 15NI...",y:"7/12, re-transform pSB1C3, biobricks 15NI, 6AI"}; var e35={x:"Extract the plasmid of 15NI,6AI",y:"7/13, extract the plasmid of 15NI, 6AI, use EcoRI and SpeI to digest the 15NI plasmid, use EcoRI and XbalI to digest the plasmid of 6AI"}; var e36={x:"Re-transform the pSB1A3 and the biobricks...",y:"7/14, re-transform the pSB1A3 and the biobricks of 15NI 6AI due to the mistakenly omitting steps of culturing E. Coli with these plasmids"};

var e41={x:"Transformed Single biobricks(1)",y:"7/15~7/17, transform the plasmids of 23LⅠ,6HⅢ,17PⅠ,2KⅠ,16MⅣ,2MⅠ, 13JⅡ,20FⅠ,8HⅡ,14HⅠ,14KⅠ,20KⅠ,4AⅠ,6IⅠ,14JⅠ,12AⅠ,4MⅠ,2IⅠ,4OⅠ At the meantime, digest the 4AⅠ, 4OⅠ, 4MⅠ with EcoRI and SpelⅠ, 23LⅠ with EcoRI and XbalⅠ, then conducting ligation digest the 6HⅢ and 17PⅠwith EcoRⅠ and SpelⅠ, with an unexpected 3-band result, owing to the higher than normal plasmid concentration."}; var e42={x:"Transformed Single biobricks(2)",y:"7/18, transform the biobricks of 8HⅡ,14KⅠ,20 KⅠ, 6IⅠ, 12AⅠ, gaining the ligation products of 23LⅠ-4AⅠ,23LⅠ- 4OⅠ,23LⅠ- 4MⅠ23LⅠ-6HⅢ, re-digest 6HⅢ with EcoRⅠ and SpelⅠ."}; var e43={x:"Transformed Single biobricks(3)",y:"7/19, transform the biobricks of 16MⅣ,20FⅠ,14HⅠ,14JⅠ,13JⅡ, use gal extract to gain the product."}; var e44={x:"Transformed Single biobricks(4)",y:"7/20, use the EcoRⅠand SpelⅠto digest 4AⅠ, 4OⅠ, 4MⅠ,use EcoRⅠand XbalⅠto digest 23L,in the meantime we use enzyme digest to test our product 4AⅠ, 4OⅠ, 4MⅠ,20 KⅠ, 6IⅠ, 12AⅠ,gain our ligation product 23LⅠ- 4MⅠ,23LⅠ-6HⅢ"};

var e51={x:"The second layer assembly(1)",y:"7/21, complete the ligation of 23LⅠ-4AⅠ,23LⅠ- 4OⅠ,23LⅠ- 4MⅠ,23LⅠ- 14KⅠ"}; var e52={x:"The second layer assembly(2)",y:"7/22,transform the biobricks of 6A and 15N,complete the ligation of 20 FⅠ-2MⅠ,13JⅡ-2M."}; var e53={x:"The second layer assembly(3)",y:"7/23~7/28,Focused on the ligation of biobricks . Till 7/28 we have successfully ligate the 23LⅠ- 4MⅠ,23LⅠ- 4OⅠ,23LⅠ-14KⅠ,20FⅠ-2MⅠ,13JⅡ-2MⅠ,23LⅠ-14JⅠ,23LⅠ-6HⅢ,4AⅠ-23LⅠ-2MⅠ,20 FⅠ-2MⅠ-23LⅠ,and 17PⅠ-23LⅠ."}; var e54={x:"The second layer assembly(4)",y:"7/29,ligated the 14JⅠ-23LⅠ-2MⅠ,4OⅠ-23LⅠ-2IⅠ,14HⅠ-2MⅠ"};

var e61={x:"The third layer assembly(1)",y:"7/30,ligated 8HⅡ-2MⅠ,4AⅠ-23LⅠ-2MⅠ-20KⅠ,15NⅠ-23LⅠ-6HⅢ,2KⅠ-16MⅣ,15NⅠ-23LⅠ-17PⅠ,2MⅠ-13JⅡ-2MⅠ-20 FⅠ-23LⅠ"}; var e62={x:"The third layer assembly(2)",y:"7/31,ligate 2MⅠ-23LⅠ- 4MⅠ,4OⅠ-23LⅠ-2IⅠ- 6IⅠ,14JⅠ-23LⅠ-2MⅠ- 6IⅠ"}; var e63={x:"The third layer assembly(3)",y:"8/1~8/2,ligate RLS5+6(2KⅠ-16MⅣ-2MⅠ-13JⅡ-2MⅠ-20 FⅠ-23LⅠ) RLS1+6(2KⅠ-16MⅣ-2MⅠ-13JⅡ-2MⅠ-20 FⅠ-23LⅠ)"}; var e64={x:"The third layer assembly(4)",y:"8/3,the ligation of 4AⅠ-23LⅠ-2MⅠ-20KⅠ,8HⅡ-2MⅠfailed,but we successfully gained the 4OⅠ-23LⅠ-2IⅠ- 6IⅠ,2MⅠ-23LⅠ- 4MⅠ,ligated the 2MⅠ-23LⅠ- 4MⅠ-12AⅠ"};

var e71={x:"Re-ligate the failure products(1)",y:"8/4~8/5, re-ligated the 23LⅠ-6HⅢ,17PⅠ-23LⅠ,4AⅠ-23LⅠ-2MⅠ-20KⅠ,test RLS1+6(2KⅠ-16MⅣ-2MⅠ-13JⅡ-2MⅠ-20 FⅠ-23LⅠ),transformed new biobricks 19CⅣ,15OⅣ,19IⅣ,6JⅢ,6LⅢ,6NⅢ,16EⅠ,8LⅡ,12LⅠ,20ⅠⅠ,6NⅠ</br></br>8/6, re-ligated 14JⅠ-23LⅠ-2MⅠ- 6IⅠ,ligated 14HⅠ-2MⅠ,6JⅢ-23LⅠ,6LⅢ-23LⅠ,15NⅠ- RLS1+6,19CⅣ-23LⅠ,15OⅣ-23LⅠ,19IⅣ-23LⅠ,23LⅠ-14KⅠ,10EⅣ-23LⅠ,15MⅣ-23LⅠ,17AⅣ-23LⅠ"}; var e72={x:"Re-ligate the failure products(2)",y:"8/7~8/10, ligated14JⅠ-23LⅠ-2MⅠ-6IⅠ,2MⅠ-14HⅠ-2MⅠ,6JⅢ-23LⅠ,6LⅢ-23LⅠ,15NⅠ-RLS1+6,19CⅣ-23LⅠ,15OⅣ-23LⅠ,19IⅣ-23LⅠ,15MⅣ-23LⅠ,17AⅣ-23LⅠ</br></br>8/11~8/12, ligated 8HⅡ-2MⅠ-14HⅠ-2MⅠ,2MⅠ-19CⅣ-23LⅠ,2MⅠ-15MⅣ-23LⅠ,2MⅠ-15OⅣ-23LⅠ,use enzyme to verify the 6JⅢ-23LⅠ,6LⅢ-23LⅠ,17AⅣ-23LⅠ"}; var e73={x:"Re-ligate the failure products(3)",y:"8/13~8/14, re-ligate 2MⅠ-19CⅣ-23LⅠ,2MⅠ-15MⅣ-23LⅠ,2MⅠ-15OⅣ-23LⅠ,ligate 2MⅠ-17AⅣ-23LⅠ,2MⅠ-6JⅢ-23LⅠ,2MⅠ-6LⅢ-23LⅠ</br></br>8/15, re-ligate 8HⅡ-2MⅠ-14HⅠ-2MⅠ,14JⅠ-23LⅠ-2MⅠ-6IⅠ,23LⅠ-14KⅠ,use PCR to amplify the 2MⅠ-19CⅣ-23LⅠ,2MⅠ-15MⅣ-23LⅠ,2MⅠ-15OⅣ-23LⅠ,2MⅠ-17AⅣ-23LⅠ"}; var e74={x:"Re-ligate the failure products(4)",y:"8/16, ligate 16EⅠ-2MⅠ-6LⅢ-23LⅠ,16EⅠ-15OⅣ,16EⅠ-17AⅣ,16EⅠ-19CⅣ,16EⅠ-15MⅣ</br></br>8/17~8/18, ligate 4EⅠ-23LⅠ,RLS1+6-16EⅠ-15OⅣ,RLS1+6-16EⅠ-6LⅢ,RLS1+6-16EⅠ-17AⅣ,RLS1+6-16EⅠ-19CⅣ,RLS1+6-19CⅣ,16MⅣ-2KⅠ"}; var e75={x:"Re-ligate the failure products(5)",y:"8/19~8/20, ligate 8HⅡ-2MⅠ-14HⅠ-2MⅠ-23LⅠ-14KⅠ,14JⅠ-23LⅠ-2MⅠ-6IⅠ-4AⅠ-23LⅠ-2MⅠ-20KⅠ,15NⅠ-RLS,16EⅠ-2MⅠ-19CⅣ-23LⅠ- pSB1C3, 16MⅣ- RLS6</br></br>8/21~8/22, re-ligate 4OⅠ-23LⅠ-2IⅠ- 6IⅠ,14JⅠ-23LⅠ-2MⅠ-6IⅠ,23LⅠ-14KⅠ,8HⅡ-2MⅠ-14HⅠ-2MⅠ,16EⅠ-2MⅠ-19CⅣ-23LⅠ- pSB1C3,16MⅣ- RLS6"}; var e76={x:"Re-ligate the failure products(6)",y:"8/23, ligate 14JⅠ-23LⅠ-2MⅠ-6IⅠ-4AⅠ-23LⅠ-2MⅠ-20KⅠ,4OⅠ-23LⅠ-2IⅠ- 6IⅠ,8HⅡ-2MⅠ-14HⅠ-2MⅠ-23LⅠ-14KⅠ,16EⅠ-2MⅠ-19CⅣ-23LⅠ-pSB1C3,16EⅠ-15MⅣ, 16EⅠ-15OⅣ, 16EⅠ-17AⅣ, 16EⅠ-6LⅢ</br></br>8/24~8/25, 16EⅠ-15MⅣ-pSB1C3, 16EⅠ-15OⅣ-pSB1C3, 16EⅠ-17AⅣ-pSB1C3, 16EⅠ-6LⅢ-pSB1C3,16EⅠ-2MⅠ-19CⅣ-23LⅠ-pSB1C3, RLS-18OⅠ, RLS-18MⅠ, RLS-2GⅡ,k360123-k360126"}; var e00={x:"Jamboree",y:"Today is the Jamboree. You can just watch back and see what we prepare for this competition. Thank you!"};

var e81={x:"Extract plasmid: 009-13,009-3",y:"8/26, extract plasmid: 009-13,009-3. Enzyme digest 009-13,009- 3. Result shows that it is not cut completely .PCR 20 + 2 positive control.Transformation: 2 M-13 J-2 M-20 F, PSB, 2 K-16 MIV, CHL1-CHL3 (DH5 α and TrpR defects strains)"}; var e82={x:"Extract plasmid: 8H, 2M-14 H-2M",y:"8/27, extract plasmid: 8H, 2M-14 H-2M. enzyme digest 009-3, 8H, 2 M-14 H-2 M. Ligate 009-2-3.Identification of the transformation of PCR 8.26 ligation results. Cut CHL1 religate CHL1-CHL3, CHL1-CHL4.Enzyme cut PCB, 23 L, RLS1.Transformation: CHL1-CHL3 (DH5 α and TrpR defects plant), CHL1-CHL4 (DH5 α and TrpR defects plant), 009-2-3, controls."}; var e83={x:"Repeat 27th enzymes digest",y:"8/28, repeat 27th enzymes digest,ligated 009-2-3. Transformation: 18 M-RLS1, 18 O-RLS1, 2 G Ⅱ-RLS1, PSB-23 L, 009-2-3, CHL1-CHL3 (TrpR defects plant), CHL1-CHL4 (TrpR defects strains) controls. Reserve RLSF-2, PSB-1."}; var e84={x:"PCR 2 M-19 C, Enzyme cut...",y:"8/29, PCR 2 M-19 C, Enzyme cut 2 M -14 H-2 M, 14 K; transform 118,122,2M-18F,009-5,009-13,control."}; var e85={x:"Extract plasmid 18 O I...",y:"8/30, extract plasmid 18 O I, 18 M I, 2 G II-RLS1 and PSB-23 L /11 tube. PCR 2 M-18 F, and identified positive cloning, the result is positive.Enzyme cut 009-2-3, 009-1-6, 2 M-14 H-2 M. Cloning-5, 009 PCR positive. Ligate 14 K-23 L, 2 M-14 H-2 M-8 H.Transformation: 18 M-RLS-2-23 L, 18 M-RLS-3-23 L, 18 M-RLS-5-23 L, 18 M-RLS-6-23 L, 2 G-RLS-23 L-1, 2 G-RLS-23 L-4 and 16 E-PCB-23 L-4, 2 M-14 H-2 M-8 H, 14 K-23 L, controls.Reserve: 009-2-3-(4), 009-2-3-6, PCB-17, PCB-23 L-5, 2 G-RLS1-6, PCB-23 L-4, 18 M-RLS1-2, PCB-23 L-6, 2 G-RLS1-4."}; var e86={x:"PCR screening 18 O-RLS...",y:"8/31, PCR screening 18 O-RLS, 18 M- RLS RLS, 2 GII-RLS, PSB-23 L. PCR 2 M-15 M-23 L.Extract plasmid 009-5. enzyme cut 009-5 . ligated 14 H-2 M.Transformation: Plasmid 118, Plasmid 122, 14 H"}; var e87={x:"Extract plasmid 18 O, 18 M- RLS...",y:"9/1, extract plasmid 18 O, 18 M- RLS RLS, 2 GII-RLS, PSB-23 L. PCR 2 M-15 M-23 L,. PCR 2 M-17 A-23 L, 2 M-15 O-23 L, 2 M-15 M-23 L, 2 M-18 F. Enzyme cut and identificaty.Extract plasmid 009-13 (1-6), 009-14 (1-6), identify of the result of enzyme cut , ligate.Reserve: 009-14-1, 009-14-5, 009-14-6, 2 M-18 F-(1), 2 M-18 F-(2).Transformation: 009-13, 14 H-2 M, CHL1-3 (TrpR defects plant), controls."};

var e91={x:"Green light sensor assembly",y:"9/2, enzyme cut 2 G-RLS, 18 O-RLS, ligate 23L; PCB-23 L, ligate 16E.Transformation: CHL1-4 (TrpR defects plant), 118, 122,, and the Plasmid Plasmid PCB-23 L, 18 O-RLS1-23 L, controls.</br></br>9/3 enzyme cut 2 G-RLS, 2 M-13 J, 18 O-RLS, 2 M-20 F, 2 M-13 J-23 L, 2 K-16 M, 16 M IV, 2 M-18 F. Extract plasmid 009-3.Transformation: Plasmid 118, 122, 009-Plasmid 2-3-4, 009-2-3-6, 009-5-10, controls."};

var e101={x:"Reporting system assembly(1)",y:"9/4, extract plasmid 2 M-14 H-2 M, 14 H-2 M, enzyme cut ligation.extract plasmid PCB, 16 E, 2 M-13 J, 2 K, 2 M, 2 M-20 F, RLS, 2 M-17 A-23 L, 2 M-15 M-23 L, 2 M-19 C-23 L, 2 M-15 O-23 L, 2 K-16 M, RLS1-6. Enzyme cut identification.</br></br>9/5, enzyme digeat14 H, 18 O-RLS-23 L, PCB-23 L, electrophoresis, recycle.Transformation: CHL1-3 (TrpR defects plant), CHL1-4 (TrpR defects plant), 16 M Ⅳ, 20 F, 14 H, 17 A,19I、19C、15O、15M、control。"}; var e102={x:"Reporting system assembly(2)",y:"9/6, extract plasmid 2 M-14 H-2 M, and ligate.Enzyme 2 M-13 J. Extract plasmid 20 F I. Transformation: 14 H-2 M, controls.</br></br>9/7, enzyme cut 2 M I. Extract plasmid 2 M-15 O, 2 M-15 M, 2 M-19 C, 2 M-19 I, 2 M-13 J,2 M-17 , electrophoresis, enzyme cut identification. Extract plasmid 009-14. Transformation: Plasmid 118, pLPCB, Plasmid 118 & pLPCB co-transformation, 2 M since connection, 2 M-13 J Ⅱ, controls.Colonies PCR identification of 18 F."}; var e103={x:"Reporting system assembly(3)",y:"9/8, ligate 2 K-13 J. Enzyme cut 009-14, ligate 14 K-23 L, 2 M-14 H-2 M. Transformation: pLPCB, 2 M. Ligate 16 M Ⅳ, 2 M-15 O, 2 M-13 J, 2 M-15 M, 2 M-17 A, 2 M-19 C, 2 M-19 I, 14 K-23 L, 2 M-14 H, controls.</br></br>9/9, extract plasmid 009-14, 8 H, RFP. Ligate 2 K-20 F. Transformation: 2 K-13 J, 2 K , 14 H-2 M, 14 K-23 L, 009-13, controls."}; var e104={x:"Reporting system assembly(4)",y:"9/10, enzyme cut 2 K- 20 F, 2 K, PCR detection. Enzyme cut 2 M , 8 H, 15 M, 099-2-3, ligation.</br></br>9/11, extract plasmid15tubes, Enzyme cut identification. PCR 2M-13J, identification. enzyme cut14K-23L、8H、009-5. transformation:pLPCB、controls."}; var e105={x:"Reporting system assembly(5)",y:"9/12, enzyme cut2M I、8H. extract plasmid009-13、15M-23L, enzyme cutligate14H-2M.</br></br>9/13, enzyme cut13J, phosphorylation2M、2K;enzyme cut18F. detectionCHL1-3、CHL1-4. ligate2Mself-ligate、2Kself-ligate、2K-13J、2K-16M、18F-2K-17A、2K-15M. colony PCR 15M-23L. enzyme cut009-2、009-3、009-4. Colony PCR identification transformation products. Blue Light Sensor test."}; var e111={x:"The fifth layer assembly(1)",y:"9/14, enzyme cut009-2、009-3、009-4、17A IV, recycle, ligate009-2+C、009-3+C、009-4+C、009-2-3+009-4、009-2-3self-ligate.</br>ligate2K、2M, enzyme cut detection.</br> Colony PCR identification transformation products. transformation:009-2、009-3、009-4、009-2-3、009-2-3-4、2M-14H-2M、009-13、2M-17A-right、2M-17A-left、18F-2K-17A、2Kself-ligate、2Mself-ligate、16MⅣ、controls. "}; var e112={x:"The fifth layer assembly(2)",y:"9/15, enzyme cut2M-13J、2K-20F、17A. ligate2M-13J-2K-20F、18F-2K-15O、GRE+118、2K-15O、2K-20F、13J-20F.</br>enzyme cut14H-2M, 2M-14H-2M, colony PCR. ligate009-2-3+009-4. </br>Blue Light Sensor test. "}; var e113={x:"The fifth layer assembly(3)",y:"9/16, extract plasmid 009 2-3-4, 009,-13, 14 H, enzyme cut and identify. Colonies PCR. Ligate 4 O-23 L-2 I + 6 I.</br>Transformation: pJT122, GRE-118, 18 F-2 M-15 O, 2 M-17 A-right, 2 M-17 A-left, 2 M-13 J-2 M-20 F, 009-2, 009-3, 009-4, 15 M-23 L, 009-5, 14 H-2 M, controls."};

var e121={x:"Second step of green light sensor assemble(1)",y:"9/17, enzyme 2 K-cut 20 F, 2 M-15 O, 18 F-2 M-15 O, 13 J-20 F, 18 F-2 M-15 O.Mention plasmid 009-2-3-4, enzyme cut detection. Connection GRE--118, 009-2-3-4.Colonies PCR product identification transformation.</br>PCR 2 M-18 F, PCR Plasmid 122.009 2-3-4 </br></br>9/18, PCR detection 18 F-15 O. Enzyme cut 16 M IV.</br></br>9/19, link 2 K-16 M, 2 M-13 J-20 F, 18 F-15 O.6 I, 23 enzyme cut L, 009-2, 009-3, 009-4.</br>PCR 2 M-18 F.Transformation: 18 F-2 M-15 O, 2 M-16 M Ⅳ, 13 J-20 K, Plasmid 122, controls."}; var e122={x:"Second step of green light sensor assemble(2)",y:"9/20, extract plasmid: 2 M-18 F,and122.Colonies PCR product identification .PCR 2 M-18 F, PCR Plasmid 122.</br></br>9/21, PCR 18 F-15 O. Enzyme cut 15 O 14 H, 6 I, 23 L, 2 M.Colonies PCR identification .</br>PCR 2 M-18 F, PCR Plasmid 122.</br></br>9/22, extract plasmid 4 O-23 L-2 I, enzyme cut 4 O-23 L-2 I, 2 M, 6 I. PCR 18 O-23 L. Ligate 14 H + 2 M."};


var e131={x:"Blue light sensor assembly(1)",y:"9/23, PCR JT112 , Cph8, 2 M-18 F. Cut CHL1 and CHL3. ligate CHL1-3.14 H, 6 I, 2 M, 4 O-23 L-2 I, 14 H-2 M.</br></br>9/24, PCR Cph8. Enzyme cut 2 M -15 O and 18 F, ligation. </br></br>9/25, PCR Cph8 , ligation18 F-15 O, enzyme cut 16 E, K30012 , J61002.</br></br>9/26, enzyme cut 2 M , 15 O-2 M."}; var e132={x:"Blue light sensor assembly(2)",y:"9/27, PCR Cph8. PCR identify 16 E-13 J-20 F, 12 G, ligate 18 F-15 O-CHL1-4 (device of blue light sensor)</br></br>9/28, enzyme cut 2 M -18 F. Enzyme cut 12 G, CHL3. PCR 122.</br></br>9/29, G, enzyme cut 12 18 F. PCR Cph8."};

var e01={x:"World Final",y:"We are now at iGEM 2011 World Championship Jamboree, MIT! Thank you for your support. You can watch back to see what we do for this competition."};


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