Team:TzuChiU Formosa/Notebook

From 2010.igem.org

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<title>慈濟大學招生宣傳網頁</title>
 
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<!--<script type="text/javascript" language="javascript">
 
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function loadHtml() {
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==Protocol==
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$("div#apDiv6").load("example.html");
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===PCR (total volume: 50 μl )===
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}
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:* 25 μl Green master mix (Promega)
 +
:* 2 μl each primer
 +
:* 2 μl template
 +
:* 19 μl ddH2O
 +
:* Cycle 95/2 min; 30x(95/1 min;56/1 min;72/2 min); 72/7 min
-
</script>-->
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===Gel Extraction- use Gel /PCR DNA Fragments Extraction Kit (Geneaid)===
 +
:* Loading the PCR products into agarose gel; run gel with 1X TAE buffer
 +
:* Excise the agarose gel slice containing relevant DNA fregments
 +
:* Transfer gel slice to a 1.5 ml microcentrifuge tube
 +
:* Add 500 μl DF buffer; incubate at 56 ℃ until gel slice has been completely dissolved
 +
:* Transfer 800 μl gel mixture to DF column
 +
:* Centrifuge 13000 rpm, 1 min
 +
:* Discard the flow-through and place the DF column back
 +
:* Add 400 μl W1 buffer; Centrifuge 13000 rpm, 1 min; Discard the flow-through
 +
:* Add 600 μl wash buffer; Centrifuge 13000 rpm, 1 min; Discard the flow-through
 +
:* Centrifuge 13000 rpm, 5 min; air- dry
 +
:* Add 50 μl ddH2O; Centrifuge 13000 rpm,1 min
 +
:* Storage at – 20℃
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<style type="text/css">
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===TA Cloning- use pGEM®-T Easy Vector (Promega)===
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<!--
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:* 1μl pGEM®-T Easy Vector
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#apDiv1 {
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:* 5μl 2X rapid ligation buffer
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position:absolute;
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:* 1μl T4 DNA ligase
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width:1162px;
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:* 3μl insert
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height:768px;
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:* 4 ℃, overnight
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top: 20px;
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#apDiv2 {
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z-index:3;
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}
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-->
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===Ligation on pSB1C3- use Elite T4 DNA ligase (Geneaid)===
-
</style>
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:* 9 μl insert
-
</head>
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:* 3 μl vector
 +
:* 2 μl 10X ligation buffer A
 +
:* 2 μl 10X ligation buffer B
 +
:* 1 μl Elite T4 DNA ligase
 +
:* 3 μl ddH2O
 +
:* 16℃, overnight
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<body background="images/慈大正門漸層背景.jpg" style="background-color:transparent">
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===Transformation===
 +
:* Take out XL-10 Gold competent cell from -80 ℃ refrigerator; put on ice
 +
:* Add 2 μl GFP generator DNA solution into competent cell
 +
:* Place on ice, 30 min
 +
:* Heat shock, 42 ℃, 90 sec
 +
:* Chill on ice, 5 min
 +
:* Add 800 μl LB medium (without antibiotics)
 +
:* Incubate at 37 ℃, 1 hr
 +
:* For TA ligation product, smear 100 μl 50 mg /ml Ampicilin, 100 μl 0.1 M IPTG and 50 μl X-gal over LB agar plate.For pSB1C3 ligation product, smear 100μl 34 mg /ml Chlorophenicol over the plate.
 +
:* Bacteria solution centrifuge 3000 rpm, 5min
 +
:* Remove 700 μl supernatant
 +
:* Mix bacteria solution; Smear 100 μl over LB agar plate
 +
:* Incubate at 37 ℃, overnight
 +
===Plasmid Extraction===
 +
:* Pick single colonies; each colony incubate with 3 ml LB medium (add antibiotics); 37℃, overnight
 +
:* Centrifuge 7500 rpm, 1 min; remove supernatant
 +
:* Resuspend bacteria with 200 μl PD1 buffer; resuspend bacterial pellet
 +
:* Add 200 μl PD2 buffer; gently mix
 +
:* Add 300 μl PD3 buffer; gently mix
 +
:* Centrifuge 13000 rpm, 15 min
 +
:* Transfer supernatant to kit filter
 +
:* Add 400 μl W1 buffer; Centrifuge 13000 rpm, 1 min; Discard the flow-through
 +
:* Add 600 μl Wash buffer; Centrifuge 13000 rpm, 1 min; Discard the flow-through
 +
:* Centrifuge 13000 rpm, 5 min; air- dry
 +
:* Dissolve DNA with 50 μl ddH2O; Centrifuge 13000 rpm,1 min
 +
:* Storage at – 20℃
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<div id="apDiv1">
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===Double Enzyme Digestion===
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  <div id="apDiv5"><img src="images/icon/logo-1.gif" width="400" height="100" /></div>
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:* 16 μl ddH2O
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  <div id="apDiv3"></div>
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:* 0.5 μl Enzyme 1
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  <div id="apDiv2">
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:* 0.5 μl Enzyme 2
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  <br>
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:* 3 μl NEB 10X buffer
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  </div>
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:* 0.3 μl NEB 10X BSA
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  <div id="apDiv4">
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:* 10 μl DNA
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    <table width="180" height="331" border="0" align="center">
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:* Incubate at 37 ℃, 3 hr
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      <tr>
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        <td width="246" height="47"><a href="tcu_money.html" target="mainFrame"><img src="images/icon/w1.png" width="185" height="45" border="0" /></a></td>
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      </tr>
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        <td><a href="http://www.saoffice.tcu.edu.tw/life/dorm.html" target="_blank"><img src="images/icon/w2.png" width="185" height="45" border="0" /></a></td>
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      </tr>
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      <tr>
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        <td><a href="http://www.oia.tcu.edu.tw/detail.php?recordID=326" target="_blank"><img src="images/icon/w4.png" width="185" height="45" border="0" /></a></td>
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      <tr>
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        <td><img src="images/icon/w5.png" width="185" height="45" border="0" /></td>
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        <td height="82"><img src="images/icon/w6.png" width="185" height="80" border="0" /></td>
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    </table>
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    <br />
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  </div>
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-
  <div id="apDiv6"><iframe src="example.html" name="mainFrame" width="715" marginwidth="0" height="625" marginheight="0" align="middle" scrolling="Auto" frameborder="0" allowtransparency="true"></iframe></div>
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</div>
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</body>
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</html>
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Latest revision as of 07:11, 4 December 2010

Contents

Protocol

PCR (total volume: 50 μl )

  • 25 μl Green master mix (Promega)
  • 2 μl each primer
  • 2 μl template
  • 19 μl ddH2O
  • Cycle 95/2 min; 30x(95/1 min;56/1 min;72/2 min); 72/7 min

Gel Extraction- use Gel /PCR DNA Fragments Extraction Kit (Geneaid)

  • Loading the PCR products into agarose gel; run gel with 1X TAE buffer
  • Excise the agarose gel slice containing relevant DNA fregments
  • Transfer gel slice to a 1.5 ml microcentrifuge tube
  • Add 500 μl DF buffer; incubate at 56 ℃ until gel slice has been completely dissolved
  • Transfer 800 μl gel mixture to DF column
  • Centrifuge 13000 rpm, 1 min
  • Discard the flow-through and place the DF column back
  • Add 400 μl W1 buffer; Centrifuge 13000 rpm, 1 min; Discard the flow-through
  • Add 600 μl wash buffer; Centrifuge 13000 rpm, 1 min; Discard the flow-through
  • Centrifuge 13000 rpm, 5 min; air- dry
  • Add 50 μl ddH2O; Centrifuge 13000 rpm,1 min
  • Storage at – 20℃

TA Cloning- use pGEM®-T Easy Vector (Promega)

  • 1μl pGEM®-T Easy Vector
  • 5μl 2X rapid ligation buffer
  • 1μl T4 DNA ligase
  • 3μl insert
  • 4 ℃, overnight

Ligation on pSB1C3- use Elite T4 DNA ligase (Geneaid)

  • 9 μl insert
  • 3 μl vector
  • 2 μl 10X ligation buffer A
  • 2 μl 10X ligation buffer B
  • 1 μl Elite T4 DNA ligase
  • 3 μl ddH2O
  • 16℃, overnight

Transformation

  • Take out XL-10 Gold competent cell from -80 ℃ refrigerator; put on ice
  • Add 2 μl GFP generator DNA solution into competent cell
  • Place on ice, 30 min
  • Heat shock, 42 ℃, 90 sec
  • Chill on ice, 5 min
  • Add 800 μl LB medium (without antibiotics)
  • Incubate at 37 ℃, 1 hr
  • For TA ligation product, smear 100 μl 50 mg /ml Ampicilin, 100 μl 0.1 M IPTG and 50 μl X-gal over LB agar plate.For pSB1C3 ligation product, smear 100μl 34 mg /ml Chlorophenicol over the plate.
  • Bacteria solution centrifuge 3000 rpm, 5min
  • Remove 700 μl supernatant
  • Mix bacteria solution; Smear 100 μl over LB agar plate
  • Incubate at 37 ℃, overnight

Plasmid Extraction

  • Pick single colonies; each colony incubate with 3 ml LB medium (add antibiotics); 37℃, overnight
  • Centrifuge 7500 rpm, 1 min; remove supernatant
  • Resuspend bacteria with 200 μl PD1 buffer; resuspend bacterial pellet
  • Add 200 μl PD2 buffer; gently mix
  • Add 300 μl PD3 buffer; gently mix
  • Centrifuge 13000 rpm, 15 min
  • Transfer supernatant to kit filter
  • Add 400 μl W1 buffer; Centrifuge 13000 rpm, 1 min; Discard the flow-through
  • Add 600 μl Wash buffer; Centrifuge 13000 rpm, 1 min; Discard the flow-through
  • Centrifuge 13000 rpm, 5 min; air- dry
  • Dissolve DNA with 50 μl ddH2O; Centrifuge 13000 rpm,1 min
  • Storage at – 20℃

Double Enzyme Digestion

  • 16 μl ddH2O
  • 0.5 μl Enzyme 1
  • 0.5 μl Enzyme 2
  • 3 μl NEB 10X buffer
  • 0.3 μl NEB 10X BSA
  • 10 μl DNA
  • Incubate at 37 ℃, 3 hr
Retrieved from "http://2010.igem.org/Team:TzuChiU_Formosa/Notebook"