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	<id>https://3demmethods.i2pc.es/index.php?action=history&amp;feed=atom&amp;title=2024Harley_40</id>
	<title>2024Harley 40 - Revision history</title>
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	<updated>2026-05-24T21:06:58Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://3demmethods.i2pc.es/index.php?title=2024Harley_40&amp;diff=4857&amp;oldid=prev</id>
		<title>WikiSysop: Created page with &quot;== Citation ==  I. Harley, F. Mazzotta, X. Shaulli, F. Scheffold, K. Landfester, and I. Lieberwirth, “Practical considerations for plunge freezing samples over 40° C for Cryo-EM,” Micron, p. 103745, 2024.  == Abstract ==  Cryo-EM is now an established tool for examining samples in their native, hydrated states—a leap made possible by vitrification. Utilising this sample preparation method to directly visualise temperature-responsive samples allows for deeper insig...&quot;</title>
		<link rel="alternate" type="text/html" href="https://3demmethods.i2pc.es/index.php?title=2024Harley_40&amp;diff=4857&amp;oldid=prev"/>
		<updated>2024-12-12T06:34:16Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;== Citation ==  I. Harley, F. Mazzotta, X. Shaulli, F. Scheffold, K. Landfester, and I. Lieberwirth, “Practical considerations for plunge freezing samples over 40° C for Cryo-EM,” Micron, p. 103745, 2024.  == Abstract ==  Cryo-EM is now an established tool for examining samples in their native, hydrated states—a leap made possible by vitrification. Utilising this sample preparation method to directly visualise temperature-responsive samples allows for deeper insig...&amp;quot;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;== Citation ==&lt;br /&gt;
&lt;br /&gt;
I. Harley, F. Mazzotta, X. Shaulli, F. Scheffold, K. Landfester, and I. Lieberwirth, “Practical considerations for plunge freezing samples over 40° C for Cryo-EM,” Micron, p. 103745, 2024.&lt;br /&gt;
&lt;br /&gt;
== Abstract ==&lt;br /&gt;
&lt;br /&gt;
Cryo-EM is now an established tool for examining samples in their native, hydrated states—a leap made possible&lt;br /&gt;
by vitrification. Utilising this sample preparation method to directly visualise temperature-responsive samples&lt;br /&gt;
allows for deeper insights into their structural behaviours under functional conditions. This requires samples to&lt;br /&gt;
be plunge-frozen at elevated temperatures and presents additional challenges, including condensation within the&lt;br /&gt;
blotting chamber and difficulties in maintaining a stable sample temperatures. Here, we address these challenges&lt;br /&gt;
and suggest practical strategies to minimise condensation and reduce temperature fluctuations during the&lt;br /&gt;
plunge-freezing of samples at elevated temperatures (&amp;gt;40 ◦C). By preheating equipment and reducing chamber&lt;br /&gt;
humidity and blotting times, we can improve sample preservation and grid reproducibility. These considerations&lt;br /&gt;
are then demonstrated on poly(N-isopropylacrylamide) microgels, which exhibit a volume phase transition due&lt;br /&gt;
to temperature changes.&lt;br /&gt;
&lt;br /&gt;
== Keywords ==&lt;br /&gt;
&lt;br /&gt;
== Links ==&lt;br /&gt;
&lt;br /&gt;
https://www.sciencedirect.com/science/article/pii/S0968432824001628&lt;br /&gt;
&lt;br /&gt;
== Related software ==&lt;br /&gt;
&lt;br /&gt;
== Related methods ==&lt;br /&gt;
&lt;br /&gt;
== Comments ==&lt;/div&gt;</summary>
		<author><name>WikiSysop</name></author>
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