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	<title>Saliva DNA Extraction - Revision history</title>
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	<updated>2026-10-18T02:14:55Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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		<id>https://eln.excellgen.com/index.php?title=Saliva_DNA_Extraction&amp;diff=15254&amp;oldid=prev</id>
		<title>Paul.xu: Created page with &quot;Saliva samples were collected from volunteers of 18-25 years of the Districts Abbottabad and Mansehra, Pakistan. Proper instructions were provided to the volunteers for vigoro...&quot;</title>
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		<updated>2016-08-31T21:03:08Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;Saliva samples were collected from volunteers of 18-25 years of the Districts Abbottabad and Mansehra, Pakistan. Proper instructions were provided to the volunteers for vigoro...&amp;quot;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Saliva samples were collected from volunteers of 18-25 years of the Districts Abbottabad and Mansehra, Pakistan. Proper instructions were provided to the volunteers for vigorously rinsing mouth for one and a half minutes, and brushing teeth thereafter. Each subject was given 3-5/mL of 5% sucrose solution for rinsing mouth for two to three minutes and then spit into 15/mL sterile specimen tube, the swab thus obtained were stored at -20 °C till processing with our modified protocol of Ralser [7]. DNA was isolated by taking 1.00/mL of liquid salivain 1.5/mL eppendorf tube. 100 µL of lysis solution (2/mL lysis buffer + 10 µL of Proteinase K + 3 µL of marcaptoethanol) was added to saliva sample and was mixed well. Sample was then incubated at 56 °C for 1:30 min. After incubation 600 µL of Phenol:Chloroform (1:1) solution was added and was incubated at once for 5 min at room temperature. Sample was then centrifuged at 10,000 rpm for 10 min and supernatant was transferred into a fresh tube very carefully. Equal volume of isopropanol was added to the subjected supernatant and was incubated at 20 °C for 20 min. Sample was centrifuged again at 10,000 rpm for 15 min and upper layer was discarded and pellet was washed with 70% ethanol. Ethanol was discarded after centrifugation at 8,000 rpm for 5 min and pellet was air-dried. Thirty micro litre of double distilled water was added to the dried DNA pellet and was incubated at 56 °C for 10 min. DNA quality and quantity was then measured with Agarose gel electrophoresis.&lt;br /&gt;
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[[Category:QPCR RT-PCR]][[Category:Protocols]]&lt;/div&gt;</summary>
		<author><name>Paul.xu</name></author>
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