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<h2h1>Informaion of sample(gDNA) &nbsp;delivery preparation</h2><p>1) Method of gDNA delivery preparation</ph1><ul> <lih1>&nbsp;DNA should be dissolved in TE buffer (Tris 10mM pH 8,0, 0.1 mM EDTA) or 10 mM Tris pH 8.0. Do Not Dissolve in Water.</lih1> <lih1>&nbsp;DNA requirement : total 50-100ug of gDNA with &gt;50 ng/ul</li> <li>&nbsp;Sample purity: OD260/280span id="1.8~2.0; free of protein, RNA, or other visible contamination</li> <li>&nbsp;The sender must provide at least one information among &ldquo;Sample QC data&rdquo; and &ldquo;Gel image of DNA electrophoresis&rdquo;&nbsp;</li></ul><p>2) &nbsp;Sender information</p><ul> <li>&nbsp;Name :&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</li> <li>&nbsp;Affiliation:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</li> <li>&nbsp;Address:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</li> <li>&nbsp;Telephone:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</li> <li>&nbsp;Email:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</li></ul><p>&nbsp;3)&nbsp;Sample information</p><ul> <li> <p><span style="font-size: larger"><span style="font-family: ArialC2.A0Sample.28gDNA.29_Preparation"><span styleclass="linemw-height: 150%; mso-fareast-font-family: 'Times New Roman'; mso-fareast-language: KO" lang="EN-US"><span style="mso-list: Ignore"><span style="font: 7pt 'Times New Roman'headline">&nbsp;</span></span></span><span style="line-height: 150%; mso-fareast-font-family: '맑은 고딕'; mso-fareast-language: KO" lang="EN-US"h2>Method of Sample type: DNA(gDNA) Preparation for Sending out</spanh2></span></span></ph1> </li> <li> <p><span style="font-size: larger"><span style="font-family: Arial"><span style="line-height: 150%; mso-fareast-font-family: 'Times New Roman'; mso-fareast-language: KO" lang="EN-US"><span style="mso-list: Ignore"><span style="font: 7pt 'Times New Roman'"h2>&nbsp;</spanh2></span></span><span style="line-height: 150%; mso-fareast-font-family: '맑은 고딕'; mso-fareast-language: KO" lang="EN-US">Condition: <u>DNA in TE buffer or EB buffer or equivalent. Not in water</u></span> </span></span></p> </li> <li> <pb><span style="font-size: largermedium"><span styleid="font-family: Arial1..C2.A0Sample.28gDNA.29_Preparation"><span styleclass="linemw-height: 150%; mso-fareast-font-family: 'Times New Roman'; mso-fareast-language: KO" lang="EN-US"><span style="mso-list: Ignore"><span style="font: 7pt 'Times New Roman'headline">1.&nbsp;</span></span></span><span style="line-height: 150%; mso-fareast-font-family: '맑은 고딕'; mso-fareast-language: KO" lang="EN-US">Sample QC data (</span><span style="line-height: 150%; color: red" lang="EN-US">*</span><span style="line-height: 150%; color: red; mso-fareast-font-family: '맑은 고딕'; mso-fareast-language: KO" lang="EN-US"> </span><span style="line-height: 150%; color: black; mso-fareast-font-family: '맑은 고딕'; mso-fareast-language: KO" lang="EN-US">is Essential</span><span style="line-height: 150%; mso-fareast-font-family: '맑은 고딕'; mso-fareast-language: KO" lang="EN-US">gDNA)Preparation</span></span></span></p> </li> <li> <p><span style="font-size: larger"><span style="font-family: Arial"><span style="line-height: 150%; mso-fareast-font-family: 'Times New Roman'; mso-fareast-language: KO" lang="EN-US"><span style="mso-list: Ignore"><span style="font: 7pt 'Times New Roman'">&nbsp;</span></span></spanb><span style="line-height: 150%; mso-fareast-font-family: '맑은 고딕'; mso-fareast-language: KO" lang="EN-US">Gel image of DNA electrophoresis</span></span></span>&nbsp;</p> </li></ul><p>4) DNA packing information</p><p>&nbsp; This way is only available when DNA is dissolved in TE or Tris buffer (Please read Note).<br />&nbsp;&nbsp; If not, please pack DNA with icepack in icebox and use Fedex or DHL service.</p><ul> <li>Mark sample information on tube (concentration, sample name&hellip;what you want)</li> <li>Seal the cap of tube with parafilm well</li> <li>Wrap the tube with paper towel or equivalent</li> <li>Put into the 50 ml Falcon tube and close the cap</li> <li>Send the sample with air cushion envelop by FEDEX or DHL or equivalent.</li></ul>
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<p>Please download and refer to the following documents for information on gDNA methods of preparation and delivery1)&nbsp;&nbsp;DNA should be dissolved in TE buffer (Tris 10mM pH 8,0, 0.</p><p>1mM EDTA) or 10 mM Tris pH 8. <a href="/userfiles/DNA_sample_sheet0.doc">Sample Shipping Information&nbsp;</a></p><p>2.)&nbsp;&nbsp;<a href="/userfiles/Declaration_of_Shipment_for_anyone.doc">Declaration </a>Do Not Dissolve in Water</p>
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<p><b><span style="font-size: small"><span id="2..C2.A0Sample.28gDNA.29_Requirement" class="mw-headline">2.&nbsp;Sample(gDNA) Requirement</span></span></b></p>
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<p>1)&nbsp;&nbsp;&nbsp;Amount and concentration spec.&nbsp;: over 20 ug of gDNA with &gt;50 ng/ul</p>
<p>&nbsp;This amount is required for</p>
<p>a.&nbsp;&nbsp;Whole genome sequencing (30X)</p>
<p>b.&nbsp;&nbsp;Whole exome sequencing (50X)</p>
<p>c.&nbsp;&nbsp;Genotyping</p>
<p>2)&nbsp;&nbsp;Sample(gDNA) should be&nbsp;: OD260/280=1.8~2.0; free of protein, RNA, or other visible contamination</p>
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<p><b><span style="font-size: small"><span id="3..C2.A0Sample.28gDNA.29_Packing_Information.C2.A0" class="mw-headline">3.&nbsp;Sample(gDNA) Packing Information&nbsp;</span></span></b></p>
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<p>This way is only available when DNA is dissolved in TE or Tris buffer.</p>
<p>1)&nbsp;&nbsp;If not, please pack DNA with icepack in icebox and use Fedex or DHL service</p>
<p>2)&nbsp;&nbsp;Mark sample information on tube (concentration, sample name&hellip;what you want)</p>
<p>3)&nbsp;&nbsp;Seal the cap of tube with parafilm well</p>
<p>4)&nbsp;&nbsp;Wrap the tube with paper towel or equivalent</p>
<p>5)&nbsp;&nbsp;Put into the 50 ml Falcon tube and close the cap</p>
<p>6)&nbsp;&nbsp;Send the sample with air cushion envelop by FEDEX or DHL or equivalent</p>
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<h1><b><span style="font-size: small"><span id="4..C2.A0Requirement_of_Sample.28gDNA.29_Information" class="mw-headline">4.&nbsp;Requirement of Sample(gDNA) Information</span></span></b></h1>
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<p>1)&nbsp; Sample type: DNA</p>
<p>2)&nbsp; Condition: DNA in TE buffer or EB buffer or equivalent. Not in water</p>
<p>3)&nbsp; Gel image of DNA electrophoresis</p>
<p>4)&nbsp; Species</p>
<p>5)&nbsp; No. of Tubes</p>
<p>6)&nbsp; Concentration (ng/&mu;l)</p>
<p>7)&nbsp; Volume (&mu;l)</p>
<p>8) &nbsp;Total Quantity (&mu;g)</p>
<p>9)&nbsp; OD260/280</p>
<p>10)&nbsp; OD260/230</p>
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<p><b><span style="font-size: medium">Please download and refer to the following documents for information on gDNA methods of preparation and delivery.</span></b></p>
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<p>1.<span style="color: #800000"><a href="http://papgi.org/userfiles/Method%20of%20Sample(gDNA)%20Preparation%20for%20Sending%20out.doc">Method of Sample (gDNA) Preparation for Sending out</a></span></p>
<p>2.<span style="color: #800000"><a href="http://papgi.org/userfiles/Declaration_of_Shipment_for_anyone.doc">Declaration of Shipment</a><br />
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