Team:KAIT Japan/Notebook
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+ | <meta content="ja" http-equiv="Content-Language" /> | ||
+ | <meta content="text/html; charset=utf-8" http-equiv="Content-Type" /> | ||
+ | <title>無題 1</title> | ||
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+ | </head> | ||
+ | <body> | ||
+ | <h2><span id="Protocol" class="style1">Protocol</span></h2> | ||
+ | <p class="style3"><strong>PCR</strong></p> | ||
+ | <p class="style4">1.Add 100μL of reagent solution(Table) to microtube. <br /> | ||
+ | 2.Dispense 20μL PCR solution to PCR tube. <br /> | ||
+ | 3.Amplifty target DNA with PCR program. <br /> | ||
+ | 4.Confirm the band of DNA by agar gel electrophoresis. | ||
+ | <table class="style8" style="text-align: center; margin-left: 120px"> | ||
+ | <tr class="style5"> | ||
+ | <td class="style9"> | ||
+ | <p class="MsoNormal"><span lang="EN-US">reagent name<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | <td class="style9">Volume(μL)</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td class="style5"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size: 12.0pt; mso-fareast-font-family: "MS 明朝"; mso-font-kerning: 1.0pt; mso-ansi-language: EN-US; mso-fareast-language: JA; mso-bidi-language: AR-SA"> | ||
+ | TaKaRa Ex Taq</span></td> | ||
+ | <td class="style5">0.5</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td class="style5"> | ||
+ | <p class="MsoNormal"><span lang="EN-US">10</span><span style="mso-ascii-font-family: "Times New Roman"; mso-hansi-font-family: "Times New Roman"">×</span><span lang="EN-US">Ex | ||
+ | Taw buffer<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | <td class="style5">10</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td class="style5"> | ||
+ | <p class="MsoNormal"><span lang="EN-US">dNDP Mixture<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | <td class="style5">8</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td class="style5"> | ||
+ | <p class="MsoNormal"> | ||
+ | <span lang="EN-US" style="mso-bidi-font-size: 12.0pt; mso-fareast-font-family: "MS 明朝"; mso-font-kerning: 1.0pt; mso-ansi-language: EN-US; mso-fareast-language: JA; mso-bidi-language: AR-SA"> | ||
+ | template DNA</span></p> | ||
+ | </td> | ||
+ | <td class="style5">2</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td class="style5" style="height: 33px"> | ||
+ | <p class="MsoNormal"><span lang="EN-US">fowerd primer<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | <td class="style5" style="height: 33px">4</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td class="style5"> | ||
+ | <p class="MsoNormal"><span lang="EN-US">reverse primer<o:p></o:p></span></p> | ||
+ | </td> | ||
+ | <td class="style5">4</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td class="style5"><span lang="EN-US">sterile water<o:p></o:p></span></td> | ||
+ | <td class="style5">71.5</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td class="style10">total</td> | ||
+ | <td class="style10">100</td> | ||
+ | </tr> | ||
+ | </table> | ||
+ | </p> | ||
+ | <p> </p> | ||
+ | <p class="style3"><strong>Transformation </strong> <br /> | ||
+ | <strong> Preparation of E. coli contain particular plasmid </strong> </p> | ||
+ | <p class="style4">1.Incubate frozen competent cell on the ice. <br /> | ||
+ | 2.Add 2μL of plasmid to competent cell. <br /> | ||
+ | 3.Incubate for 15 minutes on the ice.<br /> | ||
+ | 4.Incubate for 45 seconds at 42°C. <br /> | ||
+ | 5.Incubate for 2 minutes on the ice. <br /> | ||
+ | 6.Add 250μL LB medium and cultivate for 1 hour at 37°C.<br /> | ||
+ | 7.Spread culture medium on LB agar plate with appropriate antibiotic. <br /> | ||
+ | 8.Incubate over night at 37°C. </p> | ||
+ | <p> </p> | ||
+ | <p class="style3"><strong>Restriction enzyme digestion of DNA </strong> </p> | ||
+ | <p class="style4">1.Mix DNA and restriction enzyme(Table). <br /> | ||
+ | 2.Incubate over night at 37°C. <br /> | ||
+ | 3.Confirm the band of DNA by agar gel electrophoresis. | ||
+ | <table class="style8"> | ||
+ | <tr class="style9"> | ||
+ | <td class="style12">reagent name</td> | ||
+ | <td class="style12">Volume(μL)</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td class="style11">DNA</td> | ||
+ | <td class="style11">15</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td class="style11">EcoR I</td> | ||
+ | <td class="style11">1</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td class="style11">Xba I</td> | ||
+ | <td class="style11">1</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td class="style11">buffer M</td> | ||
+ | <td class="style11">2</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td class="style11">steril water</td> | ||
+ | <td class="style11">1</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td class="style13">total</td> | ||
+ | <td class="style13">20</td> | ||
+ | </tr> | ||
+ | </table> | ||
+ | </p> | ||
+ | <p> </p> | ||
+ | <p class="style3"><span class="style14"><strong>Plasmid extraction</strong></span><br class="style14" /> | ||
+ | <span class="style14"><strong> Preparation of plasmid extracted from E. coli | ||
+ | </strong></span> </p> | ||
+ | <p class="style4">1. Pick up single colony from agar plate and cultivate it in | ||
+ | 20 mL LB medium containing <br /> | ||
+ | appropriate antibiotic overnight at 37°C.<br /> | ||
+ | 2. Move the culture medium to 50 mL falcon.<br /> | ||
+ | 3. Centrifuge for 5 minutes at 6000rpm and 4 °C and discard solution.<br /> | ||
+ | 4. Add 2 mL Solution1, the pellet.<br /> | ||
+ | 5. Add 4 mL Solution 2, invert tube and stored 3 minutes on ice.<br /> | ||
+ | 6. Add 3 mL Solution 3, invert tube and stored 5 minutes on ice. <br /> | ||
+ | 7. Centrifuge for 10 minutes at 9,500rpm and 4 °C.<br /> | ||
+ | 10.Take aqueous layer to new 50 mL falcon. <br /> | ||
+ | 11.Add 40 μL RNase, invert tube and incubate for 30 minutes.<br /> | ||
+ | 12.Add 2 mL phenol chloroform mixture.<br /> | ||
+ | 13.Centrifuge for 5 minutes at 9,500rpm and 4 °C. <br /> | ||
+ | 14.Take supernatant to new 50 mL falcon.<br /> | ||
+ | 15.Add 3 mL chloroform solution and misce.<br /> | ||
+ | 16.Centrifuge for 3 minutes at 9,500rpm and 4 °C.<br /> | ||
+ | 17.Take 3 mL supernatant to new 50 mL falcon. <br /> | ||
+ | 18.Add 300 μL sodium acetate.<br /> | ||
+ | 19.Add 7.5 mL 100%ethanol. <br /> | ||
+ | 20.Centrifuge for 20 minutes at 9,500rpm and 4 °C and discard solution.<br /> | ||
+ | 21.Add 8 mL 70% ethanol.<br /> | ||
+ | 22.Centrifuge for 20 minutes at 9,500rpm and 4 °C and discard solution.<br /> | ||
+ | 23.Add 50 μL TE buffer and tapping.<br /> | ||
+ | 24.Preserve at freezer.</p> | ||
+ | <p class="style4"> </p> | ||
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Latest revision as of 17:07, 5 October 2011