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	<title>bomb.bio | Emily Junkins | Activity</title>
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				<title>Emily Junkins replied to the topic SARS-CoV-2 Purification (Viral Transfer Media) - BOMB extraction protocol in the forum COVID-19</title>
				<link>https://bomb.bio/forums/topic/the-official-sars-cov-2-bomb-extraction-protocol/#post-9316</link>
				<pubDate>Sat, 18 Apr 2020 15:19:13 +1200</pubDate>

									<content:encoded><![CDATA[<p>Hi all,</p>
<p>We have been able to test this protocol on real samples and see it work, but with less efficiency compared to spin column extraction. We&#8217;d like to keep using this protocol for kit-less automation but looking for ways to increase extraction efficiency. Does anyone know if using silica beads vs. carboxylated beads will make a difference, I&hellip;<span class="activity-read-more" id="activity-read-more-4573"><a href="https://bomb.bio/forums/topic/the-official-sars-cov-2-bomb-extraction-protocol/#post-9316" rel="nofollow ugc">Read more</a></span></p>
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				<title>Emily Junkins replied to the topic Hillbilly Bead Viral RNA Extraction Protocol - BOMB Community in the forum COVID-19</title>
				<link>https://bomb.bio/forums/topic/hillbilly-bead-viral-rna-extraction-protocol-bomb-community/#post-9269</link>
				<pubDate>Mon, 06 Apr 2020 15:10:10 +1200</pubDate>

									<content:encoded><![CDATA[<p>Hi all,</p>
<p>We are about to try the new BOMB COVID-19 extraction, this is nearly identical to how we prepare for NGS and have good results, so I am very excited to get it working and automated (we&#8217;ll share the programming for the opentron system once it gets going). I do want to share though that we added 80mM of DTT to the lysis buffer with GTC&hellip;<span class="activity-read-more" id="activity-read-more-4526"><a href="https://bomb.bio/forums/topic/hillbilly-bead-viral-rna-extraction-protocol-bomb-community/#post-9269" rel="nofollow ugc">Read more</a></span></p>
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				<title>Emily Junkins replied to the topic  in the forum Hillbilly Bead Viral RNA Extraction Protocol - BOMB Community</title>
				<link>https://bomb.bio/forums/reply/8992/#post-8998</link>
				<pubDate>Fri, 03 Apr 2020 17:05:54 +1200</pubDate>

									<content:encoded><![CDATA[<p>Hi everyone,</p>
<p>I am working with Bradley Stevenson and wanted to ask a few more questions. We are still using the above <a href="https://bomb.bio/forums/topic/bomb-protocol-8-2-rna-extraction-from-mammalian-cells-using-gitc-lysis/#post-8992" rel="nofollow ugc">procedure</a> with the Sera-Mag prepped beads without PEG. I saw another <a href="https://bomb.bio/forums/topic/sera-mag-speedbead/#post-2276" rel="nofollow ugc">thread</a> here about bead clumping (specifically carboxylated beads) that suggested it could be both a GTC issue and/or a nucleic acid concentration issue.</p>
<p>1. Your&hellip;<span class="activity-read-more" id="activity-read-more-4497"><a href="https://bomb.bio/forums/reply/8992/#post-8998" rel="nofollow ugc">Read more</a></span></p>
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				<title>Emily Junkins became a registered member</title>
				<link>https://bomb.bio/activity/p/4495/</link>
				<pubDate>Fri, 03 Apr 2020 16:46:47 +1200</pubDate>

				
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