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<rss version="2.0"><channel><description>Light microscopy at Bruker Fluorescence Microscopy division.&#xA;#lightsheet #multiphoton #superresolution #screening&#xA;Cell biologist in my previous life. Alumnus @mpicbg.bsky.social&#xA; @turkubioscience.bsky.social‬</description><link>https://bsky.app/profile/ichajaroslav.bsky.social</link><title>@ichajaroslav.bsky.social - Jaroslav Icha</title><item><link>https://bsky.app/profile/ichajaroslav.bsky.social/post/3mz3o7heex22j</link><description>Tetraspanin-labeled extracellular vesicles from a recent demo of Bruker superresolution microscope Vutara VXL. The individual EV size is in 10s of nm.&#xA;&#xA;See what we can do in EV imaging including capturing EVs in tissues, automated EV analysis and quantitative reports: https://www.bruker.com/en/products-and-solutions/fluorescence-microscopy/super-resolution-microscopes/extracellular-vesicle-ev-visualization-and-quantification.html</description><pubDate>30 Oct 2026 11:24 +0000</pubDate><guid isPermaLink="false">at://did:plc:3o7tc7lt3resqlppzwxnf6pd/app.bsky.feed.post/3mz3o7heex22j</guid></item><item><link>https://bsky.app/profile/ichajaroslav.bsky.social/post/3mz3o7heex22j</link><description>Tetraspanin-labeled extracellular vesicles from a recent demo of Bruker superresolution microscope Vutara VXL. The individual EV size is in 10s of nm.&#xA;&#xA;See what we can do in EV imaging including capturing EVs in tissues, automated EV analysis and quantitative reports: https://www.bruker.com/en/products-and-solutions/fluorescence-microscopy/super-resolution-microscopes/extracellular-vesicle-ev-visualization-and-quantification.html</description><pubDate>30 Oct 2026 11:24 +0000</pubDate><guid isPermaLink="false">at://did:plc:3o7tc7lt3resqlppzwxnf6pd/app.bsky.feed.post/3mz3o7heex22j</guid></item><item><link>https://bsky.app/profile/ichajaroslav.bsky.social/post/3myzex4sg4c2c</link><description>Do laser ablation experiments have to be slow and done one sample at a time?&#xA;You know the answer is NO! 😊&#xA; &#xA;New publication from Nadia Mercader Huber lab shows how to scale laser ablation into 96-well plate format with the power of Bruker Luxendo Acquifer IM equipped with a photomanipulation module.</description><pubDate>29 Oct 2026 13:33 +0000</pubDate><guid isPermaLink="false">at://did:plc:3o7tc7lt3resqlppzwxnf6pd/app.bsky.feed.post/3myzex4sg4c2c</guid></item><item><link>https://bsky.app/profile/ichajaroslav.bsky.social/post/3myzex4sg4c2c</link><description>Do laser ablation experiments have to be slow and done one sample at a time?&#xA;You know the answer is NO! 😊&#xA; &#xA;New publication from Nadia Mercader Huber lab shows how to scale laser ablation into 96-well plate format with the power of Bruker Luxendo Acquifer IM equipped with a photomanipulation module.</description><pubDate>29 Oct 2026 13:33 +0000</pubDate><guid isPermaLink="false">at://did:plc:3o7tc7lt3resqlppzwxnf6pd/app.bsky.feed.post/3myzex4sg4c2c</guid></item><item><link>https://bsky.app/profile/ichajaroslav.bsky.social/post/3mqebhyqwh22n</link><description>I&#39;m sitting in the last session of the #EZM2026 conference and I&#39;m grateful that I could participate on behalf of @brukercorporation.bsky.social Fluorescence Microscopy. Great trip to my academic past, I was relieved that I still more or less understand what people are working on.</description><pubDate>11 Jul 2026 08:44 +0000</pubDate><guid isPermaLink="false">at://did:plc:3o7tc7lt3resqlppzwxnf6pd/app.bsky.feed.post/3mqebhyqwh22n</guid></item><item><link>https://bsky.app/profile/ichajaroslav.bsky.social/post/3mrli7cu4yk2q</link><description>This week I visited Belgium for a Bruker Luxendo HIVE server installation (Fig. 1) with a detour to the Netherlands for some Bruker Fluorescence Microscopy lightsheet and superresolution microscopy conversations.</description><pubDate>26 Jul 2026 22:58 +0000</pubDate><guid isPermaLink="false">at://did:plc:3o7tc7lt3resqlppzwxnf6pd/app.bsky.feed.post/3mrli7cu4yk2q</guid></item><item><link>https://bsky.app/profile/ichajaroslav.bsky.social/post/3mxqrn6c2a22k</link><description>I enjoyed reading this paper from Wittbrodt lab on retinal lamination, using in vitro approach of retinal organoids/assembloids.&#xA;&#xA;It adds to what we know about need for polarity cues in the developing retina and draws a parallel to invertebrate compound eye development.&#xA;https://www.cell.com/iscience/fulltext/S2589-0042(26)01059-X</description><pubDate>13 Oct 2026 10:01 +0000</pubDate><guid isPermaLink="false">at://did:plc:3o7tc7lt3resqlppzwxnf6pd/app.bsky.feed.post/3mxqrn6c2a22k</guid></item><item><link>https://bsky.app/profile/ichajaroslav.bsky.social/post/3my7paumxvs2n</link><description>New paper in eLife showing lens morphogenesis taking a very different route in medaka organoids as opposed to in vivo in the fish embryo. Wittbrodt and Zilova from COS Heidelberg as senior authors. &#xA;Video: First stage of lens formation in medaka retinal organoids. Lens precursors expressing GFP.</description><pubDate>19 Oct 2026 08:28 +0000</pubDate><guid isPermaLink="false">at://did:plc:3o7tc7lt3resqlppzwxnf6pd/app.bsky.feed.post/3my7paumxvs2n</guid></item><item><link>https://bsky.app/profile/ichajaroslav.bsky.social/post/3myetimuoyk2q</link><description>Today I want to highlight other typical lightsheet microscopy use – in toto embryo imaging with laser ablation. In a recent Biophysical J paper Timo Betz and co. from Uni of Göttingen studied how robust zebrafish gastrulation is to mechanical perturbation by laser ablation. Tl;DR: very robust.</description><pubDate>21 Oct 2026 09:28 +0000</pubDate><guid isPermaLink="false">at://did:plc:3o7tc7lt3resqlppzwxnf6pd/app.bsky.feed.post/3myetimuoyk2q</guid></item><item><link>https://bsky.app/profile/ichajaroslav.bsky.social/post/3mycfdh67l225</link><description>Today I want to highlight a study from Elvan Böke lab at CRG in Barcelona as a perfect example why it makes sense to use tissue clearing and lightsheet microscopy.</description><pubDate>20 Oct 2026 10:09 +0000</pubDate><guid isPermaLink="false">at://did:plc:3o7tc7lt3resqlppzwxnf6pd/app.bsky.feed.post/3mycfdh67l225</guid></item><item><link>https://bsky.app/profile/ichajaroslav.bsky.social/post/3mxzns4n6nk2h</link><description>I&#39;m happy to share that we installed the superresolution microscope Vutara VXL (by Bruker Fluorescence Microscopy), including the fluidics unit at the Hubrecht Institute. I&#39;m sure we will see great science coming out of this system.</description><pubDate>16 Oct 2026 22:46 +0000</pubDate><guid isPermaLink="false">at://did:plc:3o7tc7lt3resqlppzwxnf6pd/app.bsky.feed.post/3mxzns4n6nk2h</guid></item><item><link>https://bsky.app/profile/ichajaroslav.bsky.social/post/3myetimuoyk2q</link><description>Today I want to highlight other typical lightsheet microscopy use – in toto embryo imaging with laser ablation. In a recent Biophysical J paper Timo Betz and co. from Uni of Göttingen studied how robust zebrafish gastrulation is to mechanical perturbation by laser ablation. Tl;DR: very robust.</description><pubDate>21 Oct 2026 09:28 +0000</pubDate><guid isPermaLink="false">at://did:plc:3o7tc7lt3resqlppzwxnf6pd/app.bsky.feed.post/3myetimuoyk2q</guid></item><item><link>https://bsky.app/profile/ichajaroslav.bsky.social/post/3mycfdh67l225</link><description>Today I want to highlight a study from Elvan Böke lab at CRG in Barcelona as a perfect example why it makes sense to use tissue clearing and lightsheet microscopy.</description><pubDate>20 Oct 2026 10:09 +0000</pubDate><guid isPermaLink="false">at://did:plc:3o7tc7lt3resqlppzwxnf6pd/app.bsky.feed.post/3mycfdh67l225</guid></item><item><link>https://bsky.app/profile/ichajaroslav.bsky.social/post/3my7paumxvs2n</link><description>New paper in eLife showing lens morphogenesis taking a very different route in medaka organoids as opposed to in vivo in the fish embryo. Wittbrodt and Zilova from COS Heidelberg as senior authors. &#xA;Video: First stage of lens formation in medaka retinal organoids. Lens precursors expressing GFP.</description><pubDate>19 Oct 2026 08:28 +0000</pubDate><guid isPermaLink="false">at://did:plc:3o7tc7lt3resqlppzwxnf6pd/app.bsky.feed.post/3my7paumxvs2n</guid></item><item><link>https://bsky.app/profile/ichajaroslav.bsky.social/post/3mxzns4n6nk2h</link><description>I&#39;m happy to share that we installed the superresolution microscope Vutara VXL (by Bruker Fluorescence Microscopy), including the fluidics unit at the Hubrecht Institute. I&#39;m sure we will see great science coming out of this system.</description><pubDate>16 Oct 2026 22:46 +0000</pubDate><guid isPermaLink="false">at://did:plc:3o7tc7lt3resqlppzwxnf6pd/app.bsky.feed.post/3mxzns4n6nk2h</guid></item><item><link>https://bsky.app/profile/ichajaroslav.bsky.social/post/3mxqrn6c2a22k</link><description>I enjoyed reading this paper from Wittbrodt lab on retinal lamination, using in vitro approach of retinal organoids/assembloids.&#xA;&#xA;It adds to what we know about need for polarity cues in the developing retina and draws a parallel to invertebrate compound eye development.&#xA;https://www.cell.com/iscience/fulltext/S2589-0042(26)01059-X</description><pubDate>13 Oct 2026 10:01 +0000</pubDate><guid isPermaLink="false">at://did:plc:3o7tc7lt3resqlppzwxnf6pd/app.bsky.feed.post/3mxqrn6c2a22k</guid></item><item><link>https://bsky.app/profile/ichajaroslav.bsky.social/post/3mrli7cu4yk2q</link><description>This week I visited Belgium for a Bruker Luxendo HIVE server installation (Fig. 1) with a detour to the Netherlands for some Bruker Fluorescence Microscopy lightsheet and superresolution microscopy conversations.</description><pubDate>26 Jul 2026 22:58 +0000</pubDate><guid isPermaLink="false">at://did:plc:3o7tc7lt3resqlppzwxnf6pd/app.bsky.feed.post/3mrli7cu4yk2q</guid></item><item><link>https://bsky.app/profile/ichajaroslav.bsky.social/post/3mqebhyqwh22n</link><description>I&#39;m sitting in the last session of the #EZM2026 conference and I&#39;m grateful that I could participate on behalf of @brukercorporation.bsky.social Fluorescence Microscopy. Great trip to my academic past, I was relieved that I still more or less understand what people are working on.</description><pubDate>11 Jul 2026 08:44 +0000</pubDate><guid isPermaLink="false">at://did:plc:3o7tc7lt3resqlppzwxnf6pd/app.bsky.feed.post/3mqebhyqwh22n</guid></item><item><link>https://bsky.app/profile/ichajaroslav.bsky.social/post/3mpxqkeu3o22b</link><description>Come to the Bruker Fluorescence Microscopy booth at the #EZM2026 zebrafish meeting in Vienna this week to learn how to capture movies like this one below in high throughput.</description><pubDate>06 Jul 2026 09:09 +0000</pubDate><guid isPermaLink="false">at://did:plc:3o7tc7lt3resqlppzwxnf6pd/app.bsky.feed.post/3mpxqkeu3o22b</guid></item><item><link>https://bsky.app/profile/ichajaroslav.bsky.social/post/3mpxqkeu3o22b</link><description>Come to the Bruker Fluorescence Microscopy booth at the #EZM2026 zebrafish meeting in Vienna this week to learn how to capture movies like this one below in high throughput.</description><pubDate>06 Jul 2026 09:09 +0000</pubDate><guid isPermaLink="false">at://did:plc:3o7tc7lt3resqlppzwxnf6pd/app.bsky.feed.post/3mpxqkeu3o22b</guid></item></channel></rss>