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allow_embed="yes">https://play.vidyard.com/VdeXnzTbtAvRM3GXg1JT8Z.html?video_id=1275365&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/rErM5wRGVj8PG174N677GA/sd.mp4?6en5lnbN92o0TbEnLkX-J99d2iof_ZXZ71g1mdqV08sK5VUEqV1EAkFQJh3ipJlncecxzt6NPBXixKbVDJEreQUUXgSbsxjGznld7QBy</video:content_loc><video:duration>66</video:duration><video:tag>NEB TV</video:tag><video:tag>NGS</video:tag><video:tag>Library Preparation for Next Generation Sequencing</video:tag><video:tag>NEBNext</video:tag><video:tag>science in 60</video:tag><video:tag>next generation sequencing</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/UCVG56asFiJjxP1givEyFC</loc><video:video><video:title>NEB TV Ep 20</video:title><video:description><![CDATA[]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/OHmLfVueTeQ3EKXyOn2Tdw/5a9987c00b5ba58b4b165f.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/UCVG56asFiJjxP1givEyFC.html?video_id=1722814&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/OHmLfVueTeQ3EKXyOn2Tdw/hd.mp4?cckqB1EGipRW5jFBx_lrOUsSlSsGymcZDveeXhYpf_ErDbVjDZ_59qxSp-F7yY_oDeIIXD50jmc7T27edhQt6a11_8Ie7qKePF6pmQDX</video:content_loc><video:duration>331</video:duration><video:tag>NEB TV</video:tag><video:tag>Green</video:tag><video:tag>Labconscious</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/vTvqERbvsFW7vJM4mHKsBC</loc><video:video><video:title>NEB TV Episode 22 Technical Support</video:title><video:description><![CDATA[]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/custom/RFQF7ymiaYH-WX3OnxaXcA.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/vTvqERbvsFW7vJM4mHKsBC.html?video_id=2374322&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/0E640dHe95CLVukcCKQCXQ/hd.mp4?cflP-zj3S8ZEdm3mS-une-zBpucp7u8iEAdKIw9GWNCpqsHMsND-e077CwbJiAqWCuFKzVsCpWwbquljkjY1v-2jlgi-GRCY7RuzdgoP</video:content_loc><video:duration>437</video:duration><video:tag>NEB TV</video:tag><video:tag>neb</video:tag><video:tag>NEB TV Ep. 22</video:tag><video:tag>Tech Support</video:tag><video:tag>Technical Support</video:tag><video:tag>NEB Tech Support</video:tag><video:tag>NEB Technical Support</video:tag><video:tag>New England Biolabs</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/md7h9pXcHrK6szTB824KHS</loc><video:video><video:title>Quick Tips - Electroporation after ligation</video:title><video:description><![CDATA[This video provides tips for performing an electroporation reaction following a ligation.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/2649387/L67ZtRjmUNSzx2rOp9eI0A.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/md7h9pXcHrK6szTB824KHS.html?video_id=2649387&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/R9peDtduM7ETaCV97wPUJg/hd.mp4?AxzIpWbF4Dy_BpcMZLoLVDDp9j5MxUbJMA1exDCu7qtfOiZh8NvPriBEfBFpy3zbvq3ayveAwsBSobrbaNnWY2SQ_I3MdRHfdL9vZGNR</video:content_loc><video:duration>55</video:duration><video:tag>DNA Modifying Enzymes and Cloning Techniques</video:tag><video:tag>Quick Tips</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/1knzwYXNTaTcvUGgm6Lmfa</loc><video:video><video:title>Quick Tips - Can I make multiple mutations with the Q5 site-directed mutagenesis kit?</video:title><video:description><![CDATA[This video describes some things to consider if you want to incorporate multiple mutations into your plasmid.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/2650433/HBZQg56QB-lP-UyXRyR5uQ.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/1knzwYXNTaTcvUGgm6Lmfa.html?video_id=2650433&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/oo0gu5M1hlO1zvVKb0zOEg/sd.mp4?rENcaV_8jK9k2kyeHmGL6vIz2UMIo7WosIyZOwLhevoariDvCwozoHIMCr9LApv_IBlNy0ssQzXoF8SPqF40i173OWzXoKOnWVwBIUAp</video:content_loc><video:duration>39</video:duration><video:tag>Quick Tips</video:tag><video:tag>DNA Assembly Cloning and Mutagenesis Kits</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/JB5jJvj4ib2M4KkeWtHpg6</loc><video:video><video:title>Quick Tips - Can I shorten the protocol for the Monarch® Cleanup?</video:title><video:description><![CDATA[This video will tell you how you can shorten the length of time it takes to clean up your nucleic acid cleanup.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/2650517/2-v7cBrKgls5Tsn7WBAU4w.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/JB5jJvj4ib2M4KkeWtHpg6.html?video_id=2650517&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/7s24u0Mm9g4d4fJgbw3u6w/hd.mp4?9bChCkVyT3OP5Yvrt4QKaEA1NapQtlAupCDZVJCtRqfctUyCefGAT75X7YZKAuXCsbfg9tvwk6SkD9efRIVHq5wOA2vd9P1hn5SfLelv</video:content_loc><video:duration>23</video:duration><video:tag>Quick Tips</video:tag><video:tag>Nucleic Acid Purification</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/qyFPvAEHxSc6R4gku6io8W</loc><video:video><video:title>Quick Tips - Do I need a 5' phosphate for ligation?</video:title><video:description><![CDATA[This video provides tips for phosphorylating fragments prior to performing a ligation reaction.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/2650555/ilhfX6iG8Z2q8YX38J1SpA.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/qyFPvAEHxSc6R4gku6io8W.html?video_id=2650555&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/g6YBhAjeWMr9qR2vQVGU7A/hd.mp4?jY3NvFKzf3dhsg-zOPvvlP1gHKCCR50r-8TEAb9mJFRRH0EDwyO-CogA7BQc7a8hWYjOz9z9D4tJo5GXOu_yxHbFsLxNu7zypj5LEcwf</video:content_loc><video:duration>41</video:duration><video:tag>Quick Tips</video:tag><video:tag>DNA Modifying Enzymes and</video:tag><video:tag>ligase</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/fYdjXA8jWkVc4BdADB6xpe</loc><video:video><video:title>Quick Tips - Electroporation after ligation</video:title><video:description><![CDATA[This video provides tips for performing an electroporation reaction following a ligation.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/2653431/u9-rA8v0ydpO1Bw2ni8c1w.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/fYdjXA8jWkVc4BdADB6xpe.html?video_id=2653431&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/NiPfayNqQhylhEy6pQZNXA/hd.mp4?pJJlCWBgcvO1BHzmwhTGs-1N1xK4c0bEOcwYoJ2fyxxYaPtsOwzcJIwlLz3SmSzA2447z6o02-rRBpHQejOJxeD35AjnUbcPZ8uTXdsk</video:content_loc><video:duration>55</video:duration><video:tag>DNA Modifying Enzymes and Cloning Techniques</video:tag><video:tag>Quick Tips</video:tag><video:tag>ligase</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/i6ezWqNrbeV7SkZJKcHeXV</loc><video:video><video:title>Quick Tips - How can I avoid genomic DNA or RNA contamination in my minipreps?</video:title><video:description><![CDATA[This video gives tips on how to avoid genomic DNA or RNA contamination when using the Monarch® Miniprep Kits.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/2653535/KtTKPvLCPh73dtFY9vLtow.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/i6ezWqNrbeV7SkZJKcHeXV.html?video_id=2653535&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/t8BCirhJiZ6meTIZQJc-5g/hd.mp4?bR6tfOsHNAfBaotJDvMxjupL8LiVF5s-sgyjC29Hqg9IQ5phAAW7hxblMhd1quRlzL5PmaZpeaBXJtbkihW-21GaD_TlMkKqA-fJbsQA</video:content_loc><video:duration>36</video:duration><video:tag>Quick Tips</video:tag><video:tag>Nucleic Acid Purification</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/GxTGxqTDeomZq7SVvuorGd</loc><video:video><video:title>Quick Tips - How can I efficiently elute large DNA fragments from agarose gels?</video:title><video:description><![CDATA[This video gives tips on eluting large DNA fragments from agarose gels.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/2653627/QxI1yvt2G8szkdD3mw1PSQ.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/GxTGxqTDeomZq7SVvuorGd.html?video_id=2653627&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/Do4hsZ6aBiljvmpROkdKog/hd.mp4?JU3EZ9Nsse4S01bnAaGgAr4bHbDY6XsTwwax6uwtgZQTmjchOYbqjW804KkbJ-M5ueJJg9bcNH3NIdDDTSW71xwNWugLvcXP0kkalaPe</video:content_loc><video:duration>40</video:duration><video:tag>Quick Tips</video:tag><video:tag>Nucleic Acid Purification</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/AdLUbZzkrffDUVmmjxQ6xn</loc><video:video><video:title>Quick Tips - How can I improve the efficiency of the DpnI digestion?</video:title><video:description><![CDATA[This video gives tips on how to improve the efficiency of your DpnI digestion.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/2653658/oy7-47Pryc4aUsBTBIBddw.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/AdLUbZzkrffDUVmmjxQ6xn.html?video_id=2653658&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/pkEABsBuECwSwI4F1aDkvQ/sd.mp4?SI4LIvsnhT4GDfHH5Eonn9dqMiP8ukONXt_9rT4ba0GfjQaIzwFwcNmWtuW2WN8GTiwyhKsoGug_cOBfGVbXsucb0L1jWETVfuAzzy5Z</video:content_loc><video:duration>34</video:duration><video:tag>DNA Modifying Enzymes and Cloning Techniques</video:tag><video:tag>Quick Tips</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/dQEdEphg7J2AXAWVHuzvp9</loc><video:video><video:title>Quick Tips - How can I maximize yield when using the Monarch® Miniprep Kits?</video:title><video:description><![CDATA[This video gives tips for maximizing the yield when using the Monarch® Miniprep Kits.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/2653681/KF-wXiMA55TuH4rZk5HEKw.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/dQEdEphg7J2AXAWVHuzvp9.html?video_id=2653681&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/Pb7hvl8Dh_ucnNK2guUMhQ/hd.mp4?VMTbFK67vHYXuVa383zC72tHnggJIgKsmrDHf-2wS2yAJVC3mEZ6XGeIMApPDO-dD_OKHPxyQosd3Yq8MVh1B1i8vZHoqX-qGmBEova1</video:content_loc><video:duration>50</video:duration><video:tag>Quick Tips</video:tag><video:tag>Nucleic Acid Purification</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/wndaNvcPzXoPSDASAD4CTR</loc><video:video><video:title>Quick Tips - How can I optimize fragmentation for RNA workflows?</video:title><video:description><![CDATA[This video will help you optimize fragmentation for RNA workflows in the NEBNext product line.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/2653709/S0mbbsxBZ9LQlpcivd1_KQ.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/wndaNvcPzXoPSDASAD4CTR.html?video_id=2653709&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/AQSVENZD0rOxGAmsMrBxpw/sd.mp4?j1xh9GbFlJLocOuhWC4LbgC_cHmf7p-srczpugUhSN0vvLGKm_Xe82NdbLXIkN04-dKS3FIQiOMO_-crKUJ-dDFWzP4J8VgvyCYAGeVU</video:content_loc><video:duration>45</video:duration><video:tag>Quick Tips</video:tag><video:tag>Library Preparation for Next Generation Sequencing</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/zVBaaKQwQ9J2ndGGj4xh6k</loc><video:video><video:title>Quick Tips - How can I optimize my ligation reaction?</video:title><video:description><![CDATA[This video gives tips on how to optimize your adapter ligation reaction.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/2653764/SN31JJjkhIGQCqoZbS8k3w.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/zVBaaKQwQ9J2ndGGj4xh6k.html?video_id=2653764&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/2p4Qo6WIZGxkD-XpMqVYpQ/sd.mp4?Dai_SGCjFL_-8VNOA6Xd5YA0M8pSnNRG4oV91lSlTTpVlcH7LjnRyig7NCZlp-NoxIiV_7kMYeEcd4jt6eokGXbvF60YctHQ0NXJ3m3v</video:content_loc><video:duration>27</video:duration><video:tag>Quick Tips</video:tag><video:tag>Library Preparation for Next Generation Sequencing</video:tag><video:tag>ligase</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/RkPWyh82QypACV76zZgZV6</loc><video:video><video:title>Quick Tips - How do I apply my elution buffer to the Monarch® nucleic acid purification column?</video:title><video:description><![CDATA[This video explains the importance of placing the elution buffer in contact with the matrix for efficient elution.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/2653788/CmAqw46Wl7QS9OEWO8KYOA.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/RkPWyh82QypACV76zZgZV6.html?video_id=2653788&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/M3zC31675HObmz_raWwz7Q/hd.mp4?D64V62l7GNa8cl_8zYgINJnUCrUom0hrhXGjhVE4yhSdKVaL9g5ce7e6d5FJ8Tq7d9bNbvwCXBa1lXd8k-P-u-jjvIl37h_-0ogXNubh</video:content_loc><video:duration>26</video:duration><video:tag>Quick Tips</video:tag><video:tag>Nucleic</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/EmRTT9E9JjfZEt3Q9e65g2</loc><video:video><video:title>Quick Tips - How do I avoid adapter dimer?</video:title><video:description><![CDATA[This video provides tips on how to avoid adapter dimer.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/2653820/wv260XxWxvxDYkk36XbLqQ.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/EmRTT9E9JjfZEt3Q9e65g2.html?video_id=2653820&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/krP61VbPDNEbbKazc10LVA/sd.mp4?9e1D5ehy_0cvoKjXdN1kcHlllVGARDIijCl73LttDS5W1fvI70KsOageclTZc0Vexr6qZzmyXd8bUDJqXxkyhCFOZapw5YXmp-1UO3xg</video:content_loc><video:duration>35</video:duration><video:tag>Quick Tips</video:tag><video:tag>Library Preparation for Next Generation Sequencing</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/Pp1TLGHE2jbBFRsLBkrBJc</loc><video:video><video:title>Quick Tips - How do I calculate how much DNA to add to a ligation reaction?</video:title><video:description><![CDATA[This video provides tips for calculating the ideal insert:vector molar ratio before performing a ligation reaction.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/2653861/KzhUp1c0X-jupzPxTq4pdg.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/Pp1TLGHE2jbBFRsLBkrBJc.html?video_id=2653861&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/qy3ty3ryCqoCtwpADF-6hg/hd.mp4?UGE1amLl18p9aTdjF8o3myo84OCGx-4S4QnshfRnrTwCwfm8tRW7MDHgyX1HP2tHFX7na_a2JF2AAwsXQpfGCwZTcu3wXjbQlPsi7-Da</video:content_loc><video:duration>57</video:duration><video:tag>DNA Modifying Enzymes and Cloning Techniques</video:tag><video:tag>Quick Tips</video:tag><video:tag>ligase</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/SEXvFGMjk1XLV3UehZNr5Q</loc><video:video><video:title>Quick Tips - How do I determine the best annealing temperature for my primers?</video:title><video:description><![CDATA[This video gives tips on how to determine the best annealing temperature for your primers using the NEBaseChanger tool.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/2653963/ISmWo7iQLXL3GqjHbBUT1w.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/SEXvFGMjk1XLV3UehZNr5Q.html?video_id=2653963&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/mxfAkIYSOtCCMz8SRbOo6A/sd.mp4?8ECxIJfNiptHAb3jmU862uc7v42mR09YtXg72Fcam5agwRwv11sbhsxNmhk4cgIBWfkegq-bhJn1cJgJ9bN6MIsDWcIeZeV2I-nks_nu</video:content_loc><video:duration>39</video:duration><video:tag>Quick Tips</video:tag><video:tag>PCR Polymerases &amp; Amplification Techniques</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/AX68x4efSRFD379dV3ZbpE</loc><video:video><video:title>Quick Tips - How much should I dilute my adapter?</video:title><video:description><![CDATA[This video describes the factors that need to be taken into consideration when calculating your adapter dilution.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/2654001/vRek4UlAxULQ1db0F7PbYg.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/AX68x4efSRFD379dV3ZbpE.html?video_id=2654001&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/0P5qAhX9Y3jUdBw4PUKeyw/sd.mp4?Lqck2peT-75IgVimZU7kGoeWEDwPn2scfwJHUgChhDhw2bGJPvn3BEH2k2_PFKoFf_p8g4XoV-PzsKuLRMQZvvD_N9q7-mP7QOKnsGxb</video:content_loc><video:duration>29</video:duration><video:tag>Quick Tips</video:tag><video:tag>Library Preparation for Next Generation Sequencing</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/nNxiZxgg36nCiyK8rnx1xj</loc><video:video><video:title>Quick Tips - Is it OK if there is foam when mixing the NEBNext reagents?</video:title><video:description><![CDATA[This video will explain why there is sometimes foam when mixing the NEBNext reagents.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/2654027/8-4zVW9SEH3ahWIY5LiueQ.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/nNxiZxgg36nCiyK8rnx1xj.html?video_id=2654027&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/PCNl6O_mERFViSi444tH_Q/sd.mp4?466HbQlOoJiSmX02rcekFE0dltQglCFKRMc-q7TXHiJLcGlodBlIOYr_zUUaZRlT8ZYVOZSmXuHB6X7sFfE2EBw2aQ8ZP8VyFW69iYzu</video:content_loc><video:duration>44</video:duration><video:tag>Quick Tips</video:tag><video:tag>Library Preparation for Next Generation Sequencing</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/g7sJDbj1j7tUQPukXPERaH</loc><video:video><video:title>Quick Tips - Should I clean up my PCR before T7 endonuclease digestion?</video:title><video:description><![CDATA[This video describes situations when your DNA should be cleaned up prior to T7 endonuclease digestion. ]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/custom/_JVAt09u8td4ozXL4JIz6Q.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/g7sJDbj1j7tUQPukXPERaH.html?video_id=2654056&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/hz-0ELzL6UZRovpSqivKxw/sd.mp4?x6ggv7xfJkTOzVIhCr42XWO0zWIazu_3XnbF8kTszW7BC995Bi8BHuKDnUO6EZ2WIrBcuhDF41UGWxh_702cQltwycUcBuAP21ndAj_X</video:content_loc><video:duration>56</video:duration><video:tag>DNA Modifying Enzymes and Cloning Techniques</video:tag><video:tag>Quick Tips</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/eVjRPsTt5TNarP2xEdFquU</loc><video:video><video:title>Quick Tips - Should I do a size selection or a clean up for NEBNext Ultra DNA or RNA workflows?</video:title><video:description><![CDATA[This video will help you decide if you need to do a size selection or a simple clean up for the NEBNext Ultra DNA or RNA.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/2654077/UeUExI7Th-mGjdXCjLPEvg.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/eVjRPsTt5TNarP2xEdFquU.html?video_id=2654077&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/jEW65QuAvq6O56EnhjELoA/sd.mp4?OkeVz1EjN4iugh1KmTp3Y_P4LP4ZrKIT35oRIuwt8wi-wgdsO9caeRZiAnLW58_RhjIiiqZmfynoIL9mOdovw1N8CP4jJZd_vEM0eBmH</video:content_loc><video:duration>53</video:duration><video:tag>Quick Tips</video:tag><video:tag>Library Preparation for Next Generation Sequencing</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/kUoZ9qgvxkexADVdwUBgVm</loc><video:video><video:title>Quick Tips - Troubleshooting problematic ligation reactions</video:title><video:description><![CDATA[This video provides tips for troubleshooting difficult ligation reactions and potential upstream contributing factors.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/2654106/WSlxCjdGDoZHYzCuAHEbWQ.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/kUoZ9qgvxkexADVdwUBgVm.html?video_id=2654106&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/WIgMKwyLEB-CWAiYtqL20Q/hd.mp4?15CzN30mqSylxRLSlRGE_HyXfkb3HufLnKgs9Vt9ksh_j-MiK-Cx9Mu--pEhAzVtb-EgCCPy0qcfIG4Kg8sXPlOoI-o1YDbRFCGA6I4W</video:content_loc><video:duration>43</video:duration><video:tag>DNA Modifying Enzymes and Cloning Techniques</video:tag><video:tag>Quick Tips</video:tag><video:tag>ligase</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/KPG6SPCrzL8aMni5YRi71X</loc><video:video><video:title>Quick Tips - What do I do if my master mix has a precipitate?</video:title><video:description><![CDATA[This video explains what to do if you find a precipitate in your master mix.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/2654233/4bB0Y5hufDgtvNRkal3A4Q.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/KPG6SPCrzL8aMni5YRi71X.html?video_id=2654233&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/Y2kKyIqKpOymbPdqjSPhvA/sd.mp4?yurTQadsuFpz0x9dkqAXkwUrpUOVkDDwF-UqJz4sa7CjGtBgG_6HxCcs6_hZ7YLPazYyAumcvlqF1AFnWGtTdVVcwhqbx4mlO2O9kqcM</video:content_loc><video:duration>24</video:duration><video:tag>Quick Tips</video:tag><video:tag>PCR Polymerases &amp; Amplification Techniques</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/v7cETACJvicSon56vkf42z</loc><video:video><video:title>Quick Tips - What is PCR overcycling?</video:title><video:description><![CDATA[This video explains what overcycling in PCR is, how to identify it and how to avoid it.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/custom/OoFRytrM7P4T0C5hZj8oig.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/v7cETACJvicSon56vkf42z.html?video_id=2654273&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/bE_VauCyg0g8m7iwWTIPIg/sd.mp4?Ab0KT7Urg2wPsYiezObImC55rQT1AgH-RYs7fFFs6r6FT4IjP4oxPhwfGn5LjuIrl6RwyXCiu-Tq3_mTCMGNq1FbxQzzy4gKg2NmvrT8</video:content_loc><video:duration>32</video:duration><video:tag>Quick Tips</video:tag><video:tag>PCR Polymerases &amp; Amplification Techniques</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/KR96qHUc3kFY7Lc3A1DsiL</loc><video:video><video:title>Quick Tips - What should I do if my end repair reaction buffer has a precipitate?</video:title><video:description><![CDATA[This video explains what to do if you find a precipitate in your end repair reaction buffer.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/2654864/U91mAkT2uVIoqU8E5NKqxg.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/KR96qHUc3kFY7Lc3A1DsiL.html?video_id=2654864&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/1mX2MBEgUbKFwQ9xqfD5hw/sd.mp4?yJXQW7KMLeXQ_iF6VT5-IcdJiG6JhNdyGEid-3VUDHc4Vzq05KsvEjEl84JOx5MoW-z0n2lD6FCmFR8E2SZn_f8qA1fDVUrEhrfSCL8D</video:content_loc><video:duration>21</video:duration><video:tag>Quick Tips</video:tag><video:tag>Library Preparation for Next Generation Sequencing</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/V2zH4BQkyLGb6JMDXKuZ12</loc><video:video><video:title>Quick Tips - What size range do I choose for my DNA fragmentation?</video:title><video:description><![CDATA[This video describes some things to take into consideration when deciding on a size range for your DNA fragmentation.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/2654892/lBxaUDvy99MWBUsVr-FciQ.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/V2zH4BQkyLGb6JMDXKuZ12.html?video_id=2654892&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/ugRSehESUV8PgKB0lLhuLA/sd.mp4?HI6GczjRJuPb4je5AbPUWnjroidMBOobB2wQP4Zrz9FIbZ5EF0RRru-b-ymVv0cQ6c1Mp2RJhbK6lSGVAlkGy2O4EY8PyHt1qLk6lrxJ</video:content_loc><video:duration>32</video:duration><video:tag>Quick Tips</video:tag><video:tag>Library Preparation for Next Generation Sequencing</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/D2Jsx5byNNrGqfs397nAsH</loc><video:video><video:title>Quick Tips - When is the right time to elute SPRI beads?</video:title><video:description><![CDATA[This video explains the ideal time to elute your SPRI beads.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/2654960/fv0oY6itf37GcGxLvRwMNw.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/D2Jsx5byNNrGqfs397nAsH.html?video_id=2654960&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/2Tvnzj5oK6BEHNPZsyGP7g/sd.mp4?ev6iZOtdg9r93C4-DHaG-S0-R_GEI-PtufSyo6s9J7R1Dd8Xl_G8jZgQ2XTmDWzFuD3Zu9U1-YUJLQs3hYn1Hc9kXW-O9irAk6y0f8am</video:content_loc><video:duration>31</video:duration><video:tag>Quick Tips</video:tag><video:tag>Library Preparation for Next Generation Sequencing</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/bay8cukozQq9WBauvchzXN</loc><video:video><video:title>Quick Tips - Why do I have so many wildtype colonies?</video:title><video:description><![CDATA[This video explains why you might have a large number of wildtype colonies following a ligation and transformation reaction.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/2654996/uRXjbqXpTn-Auss9HHuZMQ.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/bay8cukozQq9WBauvchzXN.html?video_id=2654996&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/9fPqJETtu7i2-KkgCIbgHw/sd.mp4?jGtYJTy5aP7LEzh1TUHRkpTp1ZjhFRZ1Lr-cDr3dF-pUYNtI9nKGdZfSh78pcWZoFoclHRjDWUkFSeOVVzAtf9IWeUmL_4Wn-ub9DQqm</video:content_loc><video:duration>40</video:duration><video:tag>DNA Modifying Enzymes and Cloning Techniques</video:tag><video:tag>Quick Tips</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/njK4LA8QDbthzETy1mkGjb</loc><video:video><video:title>Quick Tips - Why don't my bands on a gel look correct after T7 digestion? </video:title><video:description><![CDATA[This video explains why bands on a gel may not look correct after T7 digestions.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/custom/rbsFvbUiqo1gl-HUPCahqw.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/njK4LA8QDbthzETy1mkGjb.html?video_id=2655381&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/Hp0VWflf-DUdyPWLkBYAbQ/sd.mp4?v6YK4mDX7qzquKxdvT8wW4mJ5O_t4iwM8Q2Ok-KcWKkYm2TrtOW3P1_9Tz3n7EG9JUXym5iD-qrh5pyBfaBw5UfBMirWooD2No5WFdca</video:content_loc><video:duration>49</video:duration><video:tag>DNA Modifying Enzymes and Cloning Techniques</video:tag><video:tag>Quick Tips</video:tag><video:tag>DNA bands</video:tag><video:tag>DNA digestion</video:tag><video:tag>digestion</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/aZ9usBesmvyDQsXP1DePHd</loc><video:video><video:title>Quick Tips - Why is it important to melt the agarose prior to using the Monarch DNA Gel Extraction K</video:title><video:description><![CDATA[This video explains why it is so important to completely melt your agarose prior to using the Monarch DNA Gel Extraction Kit.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/2655410/Sis9Zr62wbDM4V7J6OzzOA.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/aZ9usBesmvyDQsXP1DePHd.html?video_id=2655410&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/00ejOoj0xnOpsE1NueNc4w/sd.mp4?_JgGNpe8uyN77gQkkgisfn6bSvOhZNx2xoAI8S5ZQUzJ4U_xBHw9XzwzvPil-kqGi3foly2Ptlbs8S3IkFEnkAtJNU1A-eMBEf4-BNEo</video:content_loc><video:duration>26</video:duration><video:tag>Quick Tips</video:tag><video:tag>Nucleic Acid Purification</video:tag><video:tag>Monarch</video:tag><video:tag>DNA cleanup</video:tag><video:tag>DNA extraction</video:tag><video:tag>gel  extraction</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/QnPU4X6RiCsL8q8Txppw9h</loc><video:video><video:title>Quick Tips - Why is there precipitate in my T4 DNA ligase buffer?</video:title><video:description><![CDATA[This video explains the source of a potential white precipitate in your T4 DNA ligase buffer.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/2655449/JSqbkyByOSW2kScz_gH7Pg.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/QnPU4X6RiCsL8q8Txppw9h.html?video_id=2655449&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/_NM6H5P_8pS7eWUANVoT1Q/hd.mp4?-CXToHysSCIK-CpVpb1cA9TtDRGbg2IdkKuspnBVUsjjyojIgaKGsoPuG3pYii1RnNFl5MvSyqpBOpcuixf0WuLhB0EBr6_mfnxQBaEw</video:content_loc><video:duration>40</video:duration><video:tag>DNA Modifying Enzymes and Cloning Techniques</video:tag><video:tag>Quick Tips</video:tag><video:tag>cloning</video:tag><video:tag>ligation</video:tag><video:tag>subcloning</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/Mu1h7w7gCjeawf4PRxvt64</loc><video:video><video:title>Quick tips - What is the ideal incubation temperature for ligation?</video:title><video:description><![CDATA[This video explains the best temperature at which to perform your ligation reaction.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/2655530/-qtCgH-D5omV0tnIVDaoEA.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/Mu1h7w7gCjeawf4PRxvt64.html?video_id=2655530&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/hdqbYXHM4Q-sLP1AHGmgPw/hd.mp4?23y9uCPaJtil1Kokh3m7qXvN8L2lmDBFdrBpjLxCTrT6ATBFyfzzZTfKug7A7RBoD24cify9ePXWvBvxl-fl2ZhqL_Rv6EUSL7TEKpwg</video:content_loc><video:duration>47</video:duration><video:tag>DNA Modifying Enzymes and Cloning Techniques</video:tag><video:tag>Quick Tips</video:tag><video:tag>ligase</video:tag><video:tag>cloning</video:tag><video:tag>ligation</video:tag><video:tag>subcloning</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/dgT8tnRNoQeGCgUGpByEek</loc><video:video><video:title>Quick Tips - When is a long incubation time necessary for ligation?</video:title><video:description><![CDATA[This video explains when it's necessary to use a long incubation time for your ligation reaction.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/2655631/Tyucpw6WV3pbMqPMB9JWIQ.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/dgT8tnRNoQeGCgUGpByEek.html?video_id=2655631&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/HgqOD0FZWyUNiAdoBeQG2g/hd.mp4?i2oLWnTPn_Iwe031pMqT3jpcdpd_HuWEVcec9sDyV_ozdu8nLZ1irKSUf0bqjBB1ubcjU_PFWbVvips-hWLEPZOpq8bsoTUW8PnIlvAo</video:content_loc><video:duration>49</video:duration><video:tag>DNA Modifying Enzymes and Cloning Techniques</video:tag><video:tag>Quick Tips</video:tag><video:tag>ligase</video:tag><video:tag>cloning</video:tag><video:tag>ligation</video:tag><video:tag>subcloning</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/6siiFQukf3mxyxU9So5owM</loc><video:video><video:title>NEB TV Episode 23</video:title><video:description><![CDATA[In this video, learn the basics of Colorimetric LAMP, and how NEB and the World Mosquito Program are using this isothermal amplification method in field tests and point-of-care diagnostics.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/2794223/TR7481W8BmvIAyNUkQ4IEw.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/6siiFQukf3mxyxU9So5owM.html?video_id=2794223&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/dxJbgRgv5i4R-VhvtbYJow/hd.mp4?K7Q7cIf1PEWKSmqoA_xyvXNo7td2UasRIIj5-1Ua5wc2yj08BWaejpxnl_GVREh_RAYtrxpS5CyLA3N8bZogsglll9hl9d9rajprhbbV</video:content_loc><video:duration>476</video:duration><video:tag>NEB TV</video:tag><video:tag>Colorimetric LAMP</video:tag><video:tag>NEB TV Ep. 23</video:tag><video:tag>World Mosquito Program</video:tag><video:tag>isothermal amplification</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/J1qDxF4v4FJQbZHU9kb4q4</loc><video:video><video:title>NEB TV Episode 23</video:title><video:description><![CDATA[In this video, learn the basics of the Colorimetric LAMP, and how NEB and the World Mosquito Program are using this isothermal amplification method in field tests and point-of-care diagnostics.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/custom/gvCfVkUf77bUKAt0M3ulog.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/J1qDxF4v4FJQbZHU9kb4q4.html?video_id=3025226&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/BsGflKaKHb1_2zSGfb6mHA/hd.mp4?qnrMuSAGfl33gDr72biEq6Ku8gCUZlpbA5Lh08XY7bLnE-LhHxpBvsJIpODC6QiVkChgv48I_1DZeEJ-DUlqyaiahAXx4WRGmtIg8W27</video:content_loc><video:duration>477</video:duration><video:tag>NEB TV</video:tag><video:tag>Colorimetric LAMP</video:tag><video:tag>World Mosquito Program</video:tag><video:tag>isothermal amplification</video:tag><video:tag>NEB TV Episode 23</video:tag><video:tag>point of care</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/aDz4RiwFyByyFRsrMDXXDd</loc><video:video><video:title>Differences between electro- competent and chemically competent cells</video:title><video:description><![CDATA[Learn how electrocompetent cells and chemically competent cells differ in the way uptake of DNA is achieved.]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/custom/KhDq8b_jPdm_6XcCllgpvw.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/aDz4RiwFyByyFRsrMDXXDd.html?video_id=3041371&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/133hPM5-Q-cDQFlME51edQ/hd.mp4?espBpzoul1JyMcyr1wmeQKxUa1wZQFof6fHW3PKqUcMLOvGym0vCWL9pQWWKFUJBIJEKNldlJBavN6lg-3mL40hjZDAD9AMiSj7cHnzf</video:content_loc><video:duration>36</video:duration><video:tag>Quick Tips</video:tag><video:tag>Comp Cells</video:tag><video:tag>Competent Cells</video:tag><video:tag>transformation</video:tag><video:tag>chemically competent</video:tag><video:tag>electrocompetent</video:tag><video:tag>electroporation</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/4AVSAZrcZJy1ouUSjvmSHd</loc><video:video><video:title>NEB TV Episode 24</video:title><video:description><![CDATA[]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/3414269/wlxpMXYBHJZE4h6k4DMU0A.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/4AVSAZrcZJy1ouUSjvmSHd.html?video_id=3414269&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/txUz7vIqwmbL_-N10YDjrg/hd.mp4?3gfWO23qPwXsvMbNNrzuUYRCdbNiPmPC5z1sKa2BzQEtdK5iQ03GFEc04X9qTIlqcHy4BZfuUTKglqhGjWURhEZZ8ayTW_UCZzU4PETM</video:content_loc><video:duration>762</video:duration><video:tag>NEB TV</video:tag><video:tag>Colorimetric LAMP</video:tag><video:tag>LAMP</video:tag><video:tag>elephantiasis</video:tag><video:tag>lymphatic filariasis</video:tag><video:tag>onchocerciasis</video:tag><video:tag>river blindness</video:tag><video:tag>tick-borne illness</video:tag><video:tag>tropical diseases</video:tag><video:tag>world health</video:tag><video:tag>filarial worms</video:tag><video:tag>neglected tropical diseases</video:tag><video:tag>vector-borne diseases</video:tag></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/EXUGz2ETcGhz6dTrSWmM2o</loc><video:video><video:title>NEB TV Ep. 25 – Conservation of Biodiversity</video:title><video:description><![CDATA[In this episode, we discuss the importance of biodiversity and conservation efforts aimed at its protection, including how we can all take part in this effort. 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allow_embed="yes">https://play.vidyard.com/mCtjwM2GeDfUyYSDHBXHeZ.html?video_id=4509356&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/BH9P3nonOBnLGO0uik_6vA/hd.mp4?8cjHOwrkOZ5dZrqyoibz24VMvMoXpKmxMEf8H77jdsNIHPyN0JhRgGBMygh-pbbRqU9ntuq0AOi3VCg-oUR1vv5Wz93_7N4icmJGJbFL</video:content_loc><video:duration>47</video:duration></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/FPNjyW7qWe8KBd8s6nkEyi</loc><video:video><video:title>James Bevington Podcast</video:title><video:description><![CDATA[]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/qg_8FLLlpgReVvjQx4idLg/dd12d3fc50405451f95249.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/FPNjyW7qWe8KBd8s6nkEyi.html?video_id=9230934&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/qg_8FLLlpgReVvjQx4idLg/hd.mp4?lHjDpGlUBfKmuHzxfp7jphLruAmvcyK18qs4bD2DJbgBag0ErKoZjXxxLjrwvqvb9lKwBmxkq92aNRTAAmpQnYmnJNd-cC3E2gvvIsGl</video:content_loc><video:duration>1245</video:duration></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/PpyEESMfxAYpbfooQTWeq3</loc><video:video><video:title>Quick Tips – Input Sample Handling Upstream of RNA Purificaiton</video:title><video:description><![CDATA[Learn how to preserve your RNA sample upstream of RNA purification with Monarch Total RNA Miniprep. ]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/custom/Cr6bgIpocQHqyR0uLsukBg.jpg</video:thumbnail_loc><video:player_loc 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allow_embed="yes">https://play.vidyard.com/V4cFuwU1QUj3LYbXHbCES1.html?video_id=9489699&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/XAuiLFXCSullO6kTV2WXcw/hd.mp4?K97dm2Utcdh3BuFXm6JIu8PJsiOrVPlry7DdAchJNn9Zz9w5nn4XNq5_Ll0ILhqFEtpeeBvc0EYzte1guDRn5Bd3X9tjhLiu3VyxrWvn</video:content_loc><video:duration>72</video:duration></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/WLnu9QnawsV7d1XBQFzPWq</loc><video:video><video:title>Quick Tips- RNA Cleanup after TRIzol Extraction</video:title><video:description><![CDATA[]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/custom/wkwmpH4E6XlydxuKos1rcQ.jpg</video:thumbnail_loc><video:player_loc allow_embed="yes">https://play.vidyard.com/WLnu9QnawsV7d1XBQFzPWq.html?video_id=9489735&amp;amp;</video:player_loc><video:content_loc>https://cdn.vidyard.com/videos/20JeZLRe9haA7SAodXcdjg/hd.mp4?iitHg9htwPtoyWB5t_I9y06iCJgcc8Nl4aKWbvqfWPz4GlcanM7k4S-Q3XeTDcP1mlQXlhVtOkBo5-1Xw0UGrVAyzGt7lpwpMQhaepsx</video:content_loc><video:duration>47</video:duration></video:video></url><url><loc>https://nebtest.hubs.vidyard.com/watch/eKurvGHVmG9sP1p19bQdU8</loc><video:video><video:title>Fidelity and Bias Ligation</video:title><video:description><![CDATA[]]></video:description><video:thumbnail_loc>https://cdn.vidyard.com/thumbnails/9066894/cJR2Ze3z-GZAVBWjbtEUZw.jpg</video:thumbnail_loc><video:player_loc 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