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Team:WHU-China/Notebook
From 2011.igem.org
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| + | #countdown | ||
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| + | #visit | ||
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| + | #bottom | ||
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#daytoday | #daytoday | ||
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| + | var a2=document.body.clientHeight; | ||
| + | document.getElementById("bottom").style.top=(a2+a1).toString()+'px'; | ||
| + | document.getElementById("contact").style.top=(a2+a1+80).toString()+'px'; | ||
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<div id="protocol"> | <div id="protocol"> | ||
<img src="/wiki/images/6/6f/Whu-Protocols.png"/> | <img src="/wiki/images/6/6f/Whu-Protocols.png"/> | ||
| - | <img src="https://static.igem.org/mediawiki/2011/c/c6/Whu-protologo1.png" style="position:absolute; | + | <img src="https://static.igem.org/mediawiki/2011/c/c6/Whu-protologo1.png" style="position:absolute;left:20px;top:40px;width:300px;height:360px;"> |
| + | <div style="position:absolute;top:60px;right:30px;width:620px;font-size:15px;"> | ||
| + | • Dealing with biobricks</br> | ||
| + | • Preparation of competent cells (Using Calcium Chloride)</br> | ||
| + | • Plasmid Extraction（Using Plasmid Mini Kit）</br> | ||
| + | • Transformation (heat-shock method)</br> | ||
| + | • Cleavage with two restriction enzymes</br> | ||
| + | • Get Extraction</br> | ||
| + | • Identification of DNA by Electrophoresis</br> | ||
| + | • Ligation</br> | ||
| + | • PCR of the colony</br> | ||
| + | • Identification of DNA by Sequencing</br> | ||
| + | • Others............ | ||
</div> | </div> | ||
| + | <a href="https://2011.igem.org/Team:WHU-China/Notebook/Protocols"><img style="position:absolute;top:380px;right:100px;width:80px;height:30px" src="/wiki/images/1/14/Whu-More.png "></a> | ||
| + | </div> | ||
| + | |||
| + | |||
<div id="daytoday"> | <div id="daytoday"> | ||
| + | <img src="/wiki/images/8/83/Whu-Progress.png"/> | ||
| + | <img src="/wiki/images/0/02/Whu-Progress.jpg" style="position:absolute;left:20px;top:53px;width:400px;height:320px;"> | ||
| + | <div style="position:absolute;top:60px;right:30px;width:520px;font-size:15px;"> | ||
| + | The forth layer assembly and assembled CHL1-3:</br> | ||
| + | 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)</br> | ||
| + | 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</br> 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.</br> | ||
| + | 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..... | ||
| + | </div> | ||
| + | <a href="https://2011.igem.org/Team:WHU-China/Notebook/Daytoday"><img style="position:absolute;top:380px;right:100px;width:80px;height:30px" src="/wiki/images/1/14/Whu-More.png "></a> | ||
</div> | </div> | ||
| + | <div style="height:100px;"></div> | ||
| + | |||
| + | <div id="bottom"> | ||
| + | <image src="/wiki/images/5/58/Whu-backgroundbottom.png"/> | ||
| + | </div> | ||
| + | <div id="contact"> | ||
| + | <a href="https://2011.igem.org/wiki/index.php?title=Team:WHU-China/Notebook&action=edit"><img class="whucontact" style="position:relative;left:636px;top:38px;z-index:10;" src="/wiki/images/2/2a/Whu-Home_r1_c1.png"/></a> | ||
| + | <a href="Mailto:gubrian890512@gmail.com"><img class="whucontact" style="position:relative;left:660px;top:38px;z-index:10;" src="/wiki/images/9/97/Whu-Home_r1_c3.png"/></a> | ||
| + | <a href="https://igem.org/Main_Page"><img class="whucontact" style="position:relative;left:676px;top:38px;z-index:10;" src="/wiki/images/0/03/Whu-Home_r1_c5.png"/></a> | ||
| + | <img id="bb" src="/wiki/images/3/3c/Whu-build.jpg"/> | ||
| + | </div> | ||
</div> | </div> | ||
</body> | </body> | ||
</html> | </html> | ||
{{WHUcss}} | {{WHUcss}} | ||
Latest revision as of 02:17, 29 October 2011
• Dealing with biobricks
• Preparation of competent cells (Using Calcium Chloride)
• Plasmid Extraction（Using Plasmid Mini Kit）
• Transformation (heat-shock method)
• Cleavage with two restriction enzymes
• Get Extraction
• Identification of DNA by Electrophoresis
• Ligation
• PCR of the colony
• Identification of DNA by Sequencing
• Others............
The forth layer assembly and assembled CHL1-3:
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)
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.
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.....
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