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	<title>Cell Transfection</title>
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		<title>Transgenic cells are created via the _______ of recombinant DNA into cells.?</title>
		<link>http://www.celltransfection.com/transgenic-cells-are-created-via-the-_______-of-recombinant-dna-into-cells-182/</link>
		<comments>http://www.celltransfection.com/transgenic-cells-are-created-via-the-_______-of-recombinant-dna-into-cells-182/#comments</comments>
		<pubDate>Sat, 07 Aug 2010 19:35:40 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
				<category><![CDATA[Transfection Questions]]></category>
		<category><![CDATA[cells]]></category>
		<category><![CDATA[created]]></category>
		<category><![CDATA[into]]></category>
		<category><![CDATA[recombinant]]></category>
		<category><![CDATA[Transgenic]]></category>
		<category><![CDATA[_______]]></category>

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		<description><![CDATA[Question by deadyetpresent: Transgenic cells are created via the _______ of recombinant DNA into cells.?
A)recombination
B)transfection
C)ligation
D)restriction
E)complementation
Best answer:
Give your answer to this question below!
]]></description>
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		<title>Hi, does anyone know how many weeks/months is the eluted DNA stable in a Tris-Cl,EDTA, pH8 solution at 4dgr?</title>
		<link>http://www.celltransfection.com/hi-does-anyone-know-how-many-weeksmonths-is-the-eluted-dna-stable-in-a-tris-cledta-ph8-solution-at-4dgr-181/</link>
		<comments>http://www.celltransfection.com/hi-does-anyone-know-how-many-weeksmonths-is-the-eluted-dna-stable-in-a-tris-cledta-ph8-solution-at-4dgr-181/#comments</comments>
		<pubDate>Sat, 07 Aug 2010 19:35:39 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
				<category><![CDATA[Transfection Questions]]></category>
		<category><![CDATA[4dgr]]></category>
		<category><![CDATA[anyone]]></category>
		<category><![CDATA[eluted]]></category>
		<category><![CDATA[know]]></category>
		<category><![CDATA[many]]></category>
		<category><![CDATA[solution]]></category>
		<category><![CDATA[Stable]]></category>
		<category><![CDATA[TrisClEDTA]]></category>
		<category><![CDATA[weeks/months]]></category>

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		<description><![CDATA[Question by AndroG: Hi, does anyone know how many weeks/months is the eluted DNA stable in a Tris-Cl,EDTA, pH8 solution at 4dgr?
To be more precized, I extracted the plasmid with my gene of interest from a bacteria with the special maxi kit endo-free from Qiagen and I eluted it with a buffer which contains 10mM [...]]]></description>
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		<slash:comments>0</slash:comments>
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		<title>Global Analysis of Transcriptional Regulation in Humans</title>
		<link>http://www.celltransfection.com/global-analysis-of-transcriptional-regulation-in-humans-135/</link>
		<comments>http://www.celltransfection.com/global-analysis-of-transcriptional-regulation-in-humans-135/#comments</comments>
		<pubDate>Thu, 29 Jul 2010 19:00:00 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
				<category><![CDATA[Transfection Videos]]></category>
		<category><![CDATA[analysis]]></category>
		<category><![CDATA[Global]]></category>
		<category><![CDATA[Humans]]></category>
		<category><![CDATA[Regulation]]></category>
		<category><![CDATA[Transcriptional]]></category>

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		<description><![CDATA[				
				
Richard Myers, Ph.D. Stanford University School of Medicine NIH Intramural Sequencing Center 10th Anniversary Symposium Genome Exploration by Large-Scale DNA Sequencing: Circa 2007 and Beyond Tuesday, October 16, 2007 Masur Auditorium Building 10, Clinical Center National Institutes of Health Bethesda, Maryland More: www.genome.gov
Video Rating: 5 / 5
]]></description>
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		<slash:comments>1</slash:comments>
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		<title>Mirus Bio Transfection and Electroporation: Mechanisms and Optimization, Part 4 Introduction to Mirus Bio&#8217;s nucleic acid delivery system</title>
		<link>http://www.celltransfection.com/mirus-bio-transfection-and-electroporation-mechanisms-and-optimization-part-4-introduction-to-mirus-bios-nucleic-acid-delivery-system-133/</link>
		<comments>http://www.celltransfection.com/mirus-bio-transfection-and-electroporation-mechanisms-and-optimization-part-4-introduction-to-mirus-bios-nucleic-acid-delivery-system-133/#comments</comments>
		<pubDate>Sun, 25 Jul 2010 21:40:42 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
				<category><![CDATA[Transfection Videos]]></category>
		<category><![CDATA[acid]]></category>
		<category><![CDATA[Bio's]]></category>
		<category><![CDATA[Delivery]]></category>
		<category><![CDATA[Electroporation]]></category>
		<category><![CDATA[Introduction]]></category>
		<category><![CDATA[Mechanisms]]></category>
		<category><![CDATA[Mirus]]></category>
		<category><![CDATA[nucleic]]></category>
		<category><![CDATA[Optimization]]></category>
		<category><![CDATA[Part]]></category>
		<category><![CDATA[System]]></category>
		<category><![CDATA[Transfection]]></category>

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		<description><![CDATA[				
				
Introduction to Mirus Bio&#8217;s nucleic acid delivery system
Video Rating: 0 / 5
]]></description>
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		<title>Creating a magnetic liquid marble</title>
		<link>http://www.celltransfection.com/creating-a-magnetic-liquid-marble-166/</link>
		<comments>http://www.celltransfection.com/creating-a-magnetic-liquid-marble-166/#comments</comments>
		<pubDate>Tue, 20 Jul 2010 11:35:46 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
				<category><![CDATA[Transfection Videos]]></category>
		<category><![CDATA[Creating]]></category>
		<category><![CDATA[liquid]]></category>
		<category><![CDATA[Magnetic]]></category>
		<category><![CDATA[marble]]></category>

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		<description><![CDATA[				
				


In contrast with the microchannel-based fluidics, the manipulation of discrete droplets without using microfluidic channels is a new field. Here, a liquid droplet is not confined to a closed channel and there is no risk of it being adsorbed on a channel wall. A liquid marble, a liquid encapsulated by non-wetting powder, could be a [...]]]></description>
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		<title>PAGFP2.mov</title>
		<link>http://www.celltransfection.com/pagfp2-mov-165/</link>
		<comments>http://www.celltransfection.com/pagfp2-mov-165/#comments</comments>
		<pubDate>Tue, 20 Jul 2010 11:35:45 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
				<category><![CDATA[Transfection Videos]]></category>
		<category><![CDATA[PAGFP2.mov]]></category>

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PhotoActivatible GFP testing 2 without pre-excitation using Mercury FV1000, 20% 205 sequential Double Transfection,60X W
]]></description>
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		<title>BioTrove RapidFire High Throughput Drug Screening System and Services</title>
		<link>http://www.celltransfection.com/biotrove-rapidfire-high-throughput-drug-screening-system-and-services-162/</link>
		<comments>http://www.celltransfection.com/biotrove-rapidfire-high-throughput-drug-screening-system-and-services-162/#comments</comments>
		<pubDate>Tue, 20 Jul 2010 11:35:43 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
				<category><![CDATA[Transfection Videos]]></category>
		<category><![CDATA[BioTrove]]></category>
		<category><![CDATA[Drug]]></category>
		<category><![CDATA[High]]></category>
		<category><![CDATA[RapidFire]]></category>
		<category><![CDATA[Screening]]></category>
		<category><![CDATA[Services]]></category>
		<category><![CDATA[System]]></category>
		<category><![CDATA[Throughput]]></category>

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		<description><![CDATA[				
				
]]></description>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>zap</title>
		<link>http://www.celltransfection.com/zap-161/</link>
		<comments>http://www.celltransfection.com/zap-161/#comments</comments>
		<pubDate>Tue, 20 Jul 2010 11:35:43 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
				<category><![CDATA[Transfection Videos]]></category>

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		<description><![CDATA[				
				
transfection
Video Rating: 1 / 5
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		<title>TPP Cell Culture Flasks</title>
		<link>http://www.celltransfection.com/tpp-cell-culture-flasks-157/</link>
		<comments>http://www.celltransfection.com/tpp-cell-culture-flasks-157/#comments</comments>
		<pubDate>Tue, 20 Jul 2010 11:35:38 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
				<category><![CDATA[Transfection Videos]]></category>
		<category><![CDATA[cell]]></category>
		<category><![CDATA[Culture]]></category>
		<category><![CDATA[Flasks]]></category>

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		<description><![CDATA[				
				
Improved Cell Retrieval Benefits Better Sample Viability Enhanced Ergonomic Features
]]></description>
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		<slash:comments>0</slash:comments>
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		<title>Caco2 cysts divide forming multiple lumens</title>
		<link>http://www.celltransfection.com/caco2-cysts-divide-forming-multiple-lumens-155/</link>
		<comments>http://www.celltransfection.com/caco2-cysts-divide-forming-multiple-lumens-155/#comments</comments>
		<pubDate>Tue, 20 Jul 2010 11:35:34 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
				<category><![CDATA[Transfection Videos]]></category>
		<category><![CDATA[Caco2]]></category>
		<category><![CDATA[cysts]]></category>
		<category><![CDATA[divide]]></category>
		<category><![CDATA[forming]]></category>
		<category><![CDATA[lumens]]></category>
		<category><![CDATA[Multiple]]></category>

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When they are transfected with Cdc42 si RNa and Cholera toxin
Video Rating: 0 / 5
]]></description>
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