Team:KAIT Japan/Notebook

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<!-- *** What falls between these lines is the Alert Box!  You can remove it from your pages once you have read and understood the alert *** -->
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{{Template:KAIT_JAPAN_body}}
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{{Template:KAIT_JAPAN_1}}
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<div id="box" style="width: 700px; margin-left: 137px; padding: 5px; border: 3px solid #000; background-color: #fe2b33;">
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<div id="template" style="text-align: center; font-weight: bold; font-size: large; color: #f6f6f6; padding: 5px;">
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This is a template page. READ THESE INSTRUCTIONS.
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<div id="instructions" style="text-align: center; font-weight: normal; font-size: small; color: #f6f6f6; padding: 5px;">
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You are provided with this team page template with which to start the iGEM season.  You may choose to personalize it to fit your team but keep the same "look." Or you may choose to take your team wiki to a different level and design your own wiki.  You can find some examples <a href="https://2008.igem.org/Help:Template/Examples">HERE</a>.
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</div>
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<div id="warning" style="text-align: center; font-weight: bold; font-size: small; color: #f6f6f6; padding: 5px;">
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You <strong>MUST</strong> have a team description page, a project abstract, a complete project description, a lab notebook, and a safety page.  PLEASE keep all of your pages within your teams namespace. 
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<head>
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<meta content="ja" http-equiv="Content-Language" />
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<meta content="text/html; charset=utf-8" http-equiv="Content-Type" />
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<title>無題 1</title>
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<style type="text/css">
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</style>
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</head>
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<body>
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<h2><span id="Protocol" class="style1">Protocol</span></h2>
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<p class="style3"><strong>PCR</strong></p>
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<p class="style4">1.Add 100μL of reagent solution(Table) to microtube. <br />
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2.Dispense 20μL PCR solution to PCR tube. <br />
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3.Amplifty target DNA with PCR program. <br />
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4.Confirm the band of DNA by agar gel electrophoresis.
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<table class="style8" style="text-align: center; margin-left: 120px">
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<tr class="style5">
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<td class="style9">
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<p class="MsoNormal"><span lang="EN-US">reagent name<o:p></o:p></span></p>
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</td>
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<td class="style9">Volume(μL)</td>
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</tr>
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<tr>
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<td class="style5">
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<span lang="EN-US" style="mso-bidi-font-size: 12.0pt; mso-fareast-font-family: &quot;MS 明朝&quot;; mso-font-kerning: 1.0pt; mso-ansi-language: EN-US; mso-fareast-language: JA; mso-bidi-language: AR-SA">
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TaKaRa Ex Taq</span></td>
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<td class="style5">0.5</td>
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</tr>
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<tr>
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<td class="style5">
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<p class="MsoNormal"><span lang="EN-US">10</span><span style="mso-ascii-font-family: &quot;Times New Roman&quot;; mso-hansi-font-family: &quot;Times New Roman&quot;">×</span><span lang="EN-US">Ex
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Taw buffer<o:p></o:p></span></p>
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</td>
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<td class="style5">10</td>
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</tr>
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<tr>
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<td class="style5">
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<p class="MsoNormal"><span lang="EN-US">dNDP Mixture<o:p></o:p></span></p>
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</td>
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<td class="style5">8</td>
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</tr>
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<tr>
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<td class="style5">
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<p class="MsoNormal">
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<span lang="EN-US" style="mso-bidi-font-size: 12.0pt; mso-fareast-font-family: &quot;MS 明朝&quot;; mso-font-kerning: 1.0pt; mso-ansi-language: EN-US; mso-fareast-language: JA; mso-bidi-language: AR-SA">
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template DNA</span></p>
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</td>
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<td class="style5">2</td>
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</tr>
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<tr>
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<td class="style5" style="height: 33px">
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<p class="MsoNormal"><span lang="EN-US">fowerd primer<o:p></o:p></span></p>
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</td>
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<td class="style5" style="height: 33px">4</td>
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</tr>
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<tr>
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<td class="style5">
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<p class="MsoNormal"><span lang="EN-US">reverse primer<o:p></o:p></span></p>
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</td>
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<td class="style5">4</td>
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</tr>
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<tr>
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<td class="style5"><span lang="EN-US">sterile water<o:p></o:p></span></td>
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<td class="style5">71.5</td>
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</tr>
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<tr>
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<td class="style10">total</td>
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<td class="style10">100</td>
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</tr>
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</table>
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</p>
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<p>&nbsp;</p>
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<p class="style3"><strong>Transformation </strong> <br />
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<strong> Preparation of E. coli contain particular plasmid </strong> </p>
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<p class="style4">1.Incubate frozen competent cell on the ice. <br />
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2.Add 2μL of plasmid to competent cell. <br />
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3.Incubate for 15 minutes on the ice.<br />
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4.Incubate for 45 seconds at 42°C. <br />
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5.Incubate for 2 minutes on the ice. <br />
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6.Add 250μL LB medium and cultivate for 1 hour at 37°C.<br />
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7.Spread culture medium on LB agar plate with appropriate antibiotic. <br />
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8.Incubate over night at 37°C. </p>
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<p>&nbsp;</p>
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<p class="style3"><strong>Restriction enzyme digestion of DNA </strong> </p>
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<p class="style4">1.Mix DNA and restriction enzyme(Table). <br />
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2.Incubate over night at 37°C. <br />
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3.Confirm the band of DNA by agar gel electrophoresis.
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<table class="style8">
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<tr class="style9">
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<td class="style12">reagent name</td>
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<td class="style12">Volume(μL)</td>
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</tr>
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<tr>
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<td class="style11">DNA</td>
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<td class="style11">15</td>
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</tr>
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<tr>
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<td class="style11">EcoR I</td>
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<td class="style11">1</td>
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</tr>
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<tr>
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<td class="style11">Xba I</td>
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<td class="style11">1</td>
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</tr>
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<tr>
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<td class="style11">buffer M</td>
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<td class="style11">2</td>
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</tr>
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<tr>
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<td class="style11">steril water</td>
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<td class="style11">1</td>
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</tr>
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<tr>
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<td class="style13">total</td>
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<td class="style13">20</td>
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</tr>
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</table>
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</p>
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<p>&nbsp;</p>
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<p class="style3"><span class="style14"><strong>Plasmid extraction</strong></span><br class="style14" />
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<span class="style14"><strong> Preparation of plasmid extracted from E. coli
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</strong></span> </p>
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<p class="style4">1. Pick up single colony from agar plate and cultivate it in
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20 mL LB medium containing&nbsp;&nbsp;&nbsp; <br />
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&nbsp; appropriate antibiotic overnight at 37°C.<br />
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2. Move the culture medium to 50 mL falcon.<br />
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3. Centrifuge for 5 minutes at 6000rpm and 4 °C and discard solution.<br />
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4. Add 2 mL Solution1, the pellet.<br />
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5. Add 4 mL Solution 2, invert tube and stored 3 minutes on ice.<br />
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6. Add 3 mL Solution 3, invert tube and stored 5 minutes on ice. <br />
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7. Centrifuge for 10 minutes at 9,500rpm and 4 °C.<br />
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10.Take aqueous layer to new 50 mL falcon. <br />
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11.Add 40 μL RNase, invert tube and incubate for 30 minutes.<br />
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12.Add 2 mL phenol chloroform mixture.<br />
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13.Centrifuge for 5 minutes at 9,500rpm and 4 °C.&nbsp; <br />
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14.Take supernatant to new 50 mL falcon.<br />
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15.Add 3 mL chloroform solution and misce.<br />
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16.Centrifuge for 3 minutes at 9,500rpm and 4 °C.<br />
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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 />
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22.Centrifuge for 20 minutes at 9,500rpm and 4 °C and discard solution.<br />
 +
23.Add 50 μL TE buffer and tapping.<br />
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24.Preserve at freezer.</p>
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<p class="style4">&nbsp;</p>
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{|align="justify"
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</body>
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|You can write a background of your team here.  Give us a background of your team, the members, etc.  Or tell us more about something of your choosing.
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|[[Image:KAIT_Japan_logo.png|200px|right|frame]]
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|-
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''Tell us more about your project.  Give us background.  Use this is the abstract of your project.  Be descriptive but concise (1-2 paragraphs)''
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|[[Image:KAIT_Japan_team.png|right|frame|Your team picture]]
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|-
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|align="center"|[[Team:KAIT_Japan | Team Example]]
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|}
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<!--- The Mission, Experiments --->
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</html>
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{| style="color:#1b2c8a;background-color:#0c6;" cellpadding="3" cellspacing="1" border="1" bordercolor="#fff" width="62%" align="center"
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!align="center"|[[Team:KAIT_Japan|Home]]
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!align="center"|[[Team:KAIT_Japan/Team|Team]]
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!align="center"|[https://igem.org/Team.cgi?year=2010&team_name=KAIT_Japan Official Team Profile]
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!align="center"|[[Team:KAIT_Japan/Project|Project]]
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!align="center"|[[Team:KAIT_Japan/Parts|Parts Submitted to the Registry]]
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!align="center"|[[Team:KAIT_Japan/Modeling|Modeling]]
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!align="center"|[[Team:KAIT_Japan/Notebook|Notebook]]
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!align="center"|[[Team:KAIT_Japan/Safety|Safety]]
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!align="center"|[[Team:KAIT_Japan/Attributions|Attributions]]
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|}
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==Notebook==
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You should make use of the calendar feature on the wiki and start a lab notebook.  This may be looked at by the judges to see how your work progressed throughout the summer.  It is a very useful organizational tool as well.
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Latest revision as of 17:07, 5 October 2011

無題 2

Home Team Official Project Notebook Safety Sponsors

無題 1

Protocol

PCR

1.Add 100μL of reagent solution(Table) to microtube.
2.Dispense 20μL PCR solution to PCR tube.
3.Amplifty target DNA with PCR program.
4.Confirm the band of DNA by agar gel electrophoresis.

reagent name

Volume(μL)
TaKaRa Ex Taq 0.5

10×Ex Taw buffer

10

dNDP Mixture

8

template DNA

2

fowerd primer

4

reverse primer

4
sterile water 71.5
total 100

 

Transformation
 Preparation of E. coli contain particular plasmid

1.Incubate frozen competent cell on the ice.
2.Add 2μL of plasmid to competent cell.
3.Incubate for 15 minutes on the ice.
4.Incubate for 45 seconds at 42°C.
5.Incubate for 2 minutes on the ice.
6.Add 250μL LB medium and cultivate for 1 hour at 37°C.
7.Spread culture medium on LB agar plate with appropriate antibiotic.
8.Incubate over night at 37°C.

 

Restriction enzyme digestion of DNA

1.Mix DNA and restriction enzyme(Table).
2.Incubate over night at 37°C.
3.Confirm the band of DNA by agar gel electrophoresis.

reagent name Volume(μL)
DNA 15
EcoR I 1
Xba I 1
buffer M 2
steril water 1
total 20

 

Plasmid extraction
 Preparation of plasmid extracted from E. coli

1. Pick up single colony from agar plate and cultivate it in 20 mL LB medium containing   
  appropriate antibiotic overnight at 37°C.
2. Move the culture medium to 50 mL falcon.
3. Centrifuge for 5 minutes at 6000rpm and 4 °C and discard solution.
4. Add 2 mL Solution1, the pellet.
5. Add 4 mL Solution 2, invert tube and stored 3 minutes on ice.
6. Add 3 mL Solution 3, invert tube and stored 5 minutes on ice.
7. Centrifuge for 10 minutes at 9,500rpm and 4 °C.
10.Take aqueous layer to new 50 mL falcon.
11.Add 40 μL RNase, invert tube and incubate for 30 minutes.
12.Add 2 mL phenol chloroform mixture.
13.Centrifuge for 5 minutes at 9,500rpm and 4 °C. 
14.Take supernatant to new 50 mL falcon.
15.Add 3 mL chloroform solution and misce.
16.Centrifuge for 3 minutes at 9,500rpm and 4 °C.
17.Take 3 mL supernatant to new 50 mL falcon.
18.Add 300 μL sodium acetate.
19.Add 7.5 mL 100%ethanol.
20.Centrifuge for 20 minutes at 9,500rpm and 4 °C and discard solution.
21.Add 8 mL 70% ethanol.
22.Centrifuge for 20 minutes at 9,500rpm and 4 °C and discard solution.
23.Add 50 μL TE buffer and tapping.
24.Preserve at freezer.