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		<title>Using the NanoDrop - Revision history</title>
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		<updated>2013-06-19T11:42:25Z</updated>
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		<id>http://openwetware.org/index.php?title=Using_the_NanoDrop&amp;diff=605606&amp;oldid=prev</id>
		<title>Alex Zorychta: New page: ==Overview==  Detailed below is the procedure to use the NanoDrop machine to quantify amount of nucleic acid, specifically as prepared from [this protocol].  ==Materials==  * Sterile Water...</title>
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				<updated>2012-06-04T16:35:35Z</updated>
		
		<summary type="html">&lt;p&gt;New page: ==Overview==  Detailed below is the procedure to use the NanoDrop machine to quantify amount of nucleic acid, specifically as prepared from [this protocol].  ==Materials==  * Sterile Water...&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;==Overview==&lt;br /&gt;
&lt;br /&gt;
Detailed below is the procedure to use the NanoDrop machine to quantify amount of nucleic acid, specifically as prepared from [this protocol].&lt;br /&gt;
&lt;br /&gt;
==Materials==&lt;br /&gt;
&lt;br /&gt;
* Sterile Water&lt;br /&gt;
* Buffer without sample&lt;br /&gt;
* Sample in buffer&lt;br /&gt;
&lt;br /&gt;
==Procedure==&lt;br /&gt;
&lt;br /&gt;
'''Be very careful using the machine, the other lab is very strict about it and misuse may cause us to lose our privilege of using it.'''&lt;br /&gt;
&lt;br /&gt;
* Open up the NanoDrop application.&lt;br /&gt;
* Choose &amp;quot;Nucleic Acid&amp;quot; on the GUI.&lt;br /&gt;
* Aliquot 2 μL of sterile water on the sample space of the machine and then close it.&lt;br /&gt;
* Click &amp;quot;OK.&amp;quot; Make sure it clicks as it reads the sample.&lt;br /&gt;
* Wipe the sample space with a Kimwipe.&lt;br /&gt;
* Next, put in 2 μL of the buffer ''without the sample'' and click &amp;quot;Blank.&amp;quot; Wipe it off with a Kimwipe. ''This is our control measurement.''&lt;br /&gt;
* Next, put in 2 μL of your sample. Click &amp;quot;Measure.&amp;quot; Then clean the sample space with a Kimwipe.&lt;br /&gt;
* Lastly, put on 2 μL of sterile water again, press it down, then move it back up again, and wipe it with a Kimwipe.&lt;br /&gt;
&lt;br /&gt;
Name the file, click &amp;quot;Show Report,&amp;quot; and &amp;quot;Save Window&amp;quot; into the shared CVRC folder to access it on our own computers.&lt;br /&gt;
&lt;br /&gt;
==Notes==&lt;br /&gt;
Please feel free to post comments, questions, or improvements to this protocol. Happy to have your input!&lt;br /&gt;
&lt;br /&gt;
&amp;lt;!-- Please sign your name to your note by adding &amp;lt;font face=&amp;quot;courier&amp;quot;&amp;gt;&amp;lt;nowiki&amp;gt;'''*~~~~''':&amp;lt;/nowiki&amp;gt;&amp;lt;/font&amp;gt; to the beginning of your tip.--&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;!-- If this protocol has papers or books associated with it, list those references here.--&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Contact==&lt;br /&gt;
*Who has experience with this protocol?&lt;br /&gt;
&lt;br /&gt;
or instead, [[Talk:{{PAGENAME}}|discuss this protocol]]. &lt;br /&gt;
&lt;br /&gt;
&amp;lt;!-- You can tag this protocol with various categories.  See the [[Categories]] page for more information. --&amp;gt;&lt;br /&gt;
[[Category:Protocol]]&lt;br /&gt;
&amp;lt;!-- Move the relevant categories above this line to tag your protocol with the label&lt;br /&gt;
[[Category:Protocol]]&lt;br /&gt;
&lt;br /&gt;
[[Category:Needs attention]]&lt;br /&gt;
 &lt;br /&gt;
[[Category:In vitro]]&lt;br /&gt;
&lt;br /&gt;
[[Category:In vivo]]&lt;br /&gt;
&lt;br /&gt;
[[Category:In silico]]&lt;br /&gt;
&lt;br /&gt;
[[Category:DNA]]&lt;br /&gt;
&lt;br /&gt;
[[Category:RNA]]&lt;br /&gt;
&lt;br /&gt;
[[Category:Protein]]&lt;br /&gt;
&lt;br /&gt;
[[Category:Chemical]]&lt;br /&gt;
&lt;br /&gt;
[[Category:Escherichia coli]]&lt;br /&gt;
&lt;br /&gt;
[[Category:Yeast]]&lt;br /&gt;
--&amp;gt;&lt;/div&gt;</summary>
		<author><name>Alex Zorychta</name></author>	</entry>

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