<p><strong>In the  week from October 3, 2022, the following webinars await you in the field of gas / solid phase and especially GC and GC/MS.</strong></p>
<blockquote>
<h4><a href="https://gcms.labrulez.com/webinars"><strong>👉 DETAILS AND REGISTRATION IN THE WEBINARS SECTION</strong></a></h4>
</blockquote>
<blockquote>
<p><strong>👉 Search and filter</strong> in more than <strong>2 000 GC, LC nad MS webinars</strong>.</p>
</blockquote>
<h5><strong>1. Thermo Fisher Scientific: Contaminants in food - Sample preparation and POPs</strong></h5>
<ul>
<li>Tu, 4.10.2022, 11:00 (CEST - Prague)</li>
</ul>
<p>Webinar will cover topics like Sample preparation in food analysis or Persistent organic pollutants analysis by GC-MS/MS.</p>
<h5><strong>2. SelectScience/Agilent Technologies/Thermo Fisher Scientific/Oxford Instruments/PAL Systems/RAFA: Virtual Food Analysis Summit 2022</strong></h5>
<ul>
<li>Tu, 4.10.2022, 13:30 (CEST)</li>
</ul>
<p>Join us online, in real-time, to discuss the very latest developments in food safety analysis, food legislation and quality control, food pathogens, pesticides, mycotoxins, and more.</p>
<h5><strong>3. Agilent Technologies: Tips for Developing Successful Solid Phase Extraction Methods</strong></h5>
<ul>
<li>Tu, 4.10.2022, 17:00 (CEST)</li>
</ul>
<p>In this talk, we will discuss tips for selecting, developing, and implementing simple and successful solid phase extraction methods.</p>
<h5><strong>4. Agilent Technologies: Multiplatform Untargeted Metabolomics (LC/MS, GC/MS, CE/MS) vs Semitargeted LC/MS for Lipids and Polar Compounds</strong></h5>
<ul>
<li>We, 5.10.2022, 11:00 (CEST)</li>
</ul>
<p>Advantages and limitations of these analytical platforms will be discussed with some examples from our laboratory.</p>
<h5><strong>5. Thermo Fisher Scientific: Contaminants in food - Microplastics</strong></h5>
<ul>
<li>We, 5.10.2022, 11:00 (CEST - Prague)</li>
</ul>
<p>Topics: Microplastics analysis in food by µFTIR and chemical images, Food packaging and microplastics analyses, Pyrolysis/GC/MS for microplastic identification - benefits of HR Orbitrap mass spectrometry.</p>
<h5><strong>6. Thermo Fisher Scientific: Contaminants in food - NIAS in packaging and PFAS</strong></h5>
<ul>
<li>Th, 6.10.2022, 11:00 (CEST - Prague)</li>
</ul>
<p>Topics: NIAS in packaging and PFAS, A GC- and LC-MS workflow for determining NIAS in food packaging.</p>
<h5><strong>7. Thermo Fisher Scientific: Analysis of battery electrolytes</strong></h5>
<ul>
<li>Th, 6.10.2022, 11:00 (CEST)</li>
</ul>
<p>Learn about analytical solutions for lithium-ion battery material and structural analysis. Learn how IC, GC-MS, ICP-OES, and SEM support battery value chain from raw materials to recycling.</p>
<h5><strong>8. Agilent Technologies: Considerations when changing over from Helium to alternative carrier gases in GC</strong></h5>
<ul>
<li>Th, 6.10.2022, 11:00 (CEST)</li>
</ul>
<p>The advantages and disadvantages of switching to a different carrier gas will be discussed, as well as what the implications are.</p>
<h5><strong>9. Separation Science/Agilent Technologies: Ask the Agilent Experts - Part 3: GC and GC/MS Scientists Discuss &amp; Answer Your Most Frequently Asked Questions</strong></h5>
<ul>
<li>Th, 6.10.2022, 16:00 (CEST)</li>
</ul>
<p>Separation Science, in collaboration with Agilent, offers Part 3 of the ever popular “Ask the Agilent Experts” series panel discussion webinars.</p>
<h5><strong>10. Agilent Technologies: Indecisive About your Column Selection? Let Us Help You Choose the Correct GC Column</strong></h5>
<ul>
<li>Th, 6.10.2022, 17:00 (CEST)</li>
</ul>
<p>This talk will discuss how the various stationary phases influence selectivity, as well as how column dimensions affect peak behavior and resolution.</p>
<h5><strong>11. Agilent Technologies: Deciding What Accessories You Need for a High End UV-Vis-NIR Instrument</strong></h5>
<ul>
<li>Th, 6.10.2022, 20:00 (CEST)</li>
</ul>
<p>An examination into the types of measurements and the accessory(s) needed to gather the desired data will be made in this discussion.</p>
<h5><strong>12. Agilent Technologies: Understanding UV-Vis (-NIR) Instrument Parameters</strong></h5>
<ul>
<li>Fr, 7.10.2022, 19:00 (CEST)</li>
</ul>
<p>While making a UV-Vis (-NIR) measurement is simple, making an accurate measurement requires an understanding of instrument parameters and their effects on the measurement.</p>


Webinars LabRulezGCMS Week 40/2022

Conference CEEPC/IPM/CMSC 2022 (Day 2)

<p><strong>DataApex is pleased to announce that a new control module for the <a href="https://lcms.labrulez.com/library?from=2020&amp;instrumentationItems=27&amp;mainauthorItems=1&amp;search=Nexera&amp;to=2022">Nexera LC-40 HPLC system</a> has been released in June 2022! It is a part of <a href="https://www.dataapex.com/product/controls-lc-shimadzu-nexera?language_content_entity=en">Clarity - Shimadzu Edition Chromatography Software</a> that is dedicated to the European market. Customers can use a control module for the Nexera LC-40 HPLC system in combination with hundreds of instruments supported in Clarity, including the <a href="https://gcms.labrulez.com/library?instrumentationItems=1&amp;mainauthorItems=1&amp;search=nexis+2030">Shimadzu Nexis GC-2030</a>.</strong></p>
<p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/driven_by_clarity_1024_1_5c9d9d86ac/driven-by-clarity-1024-1.webp" alt="DataApex: Shimadzu Nexera LC-40 HPLC and Nexis GC-2030 systems controlled by Clarity Chromatography Software"/></p>
<p><a href="https://gcms.labrulez.com/library?mainauthorItems=95&amp;search=clarity"><strong>Clarity Chromatography Software</strong></a> has a strong position in the <strong>chromatography data systems</strong> market. Clarity is highly regarded for its <strong>intuitive</strong> approach, excellent <strong>performance</strong>, <strong>cost-effectiveness</strong>, and proficient <strong>technical support</strong>. Clarity can control <a href="https://www.dataapex.com/controls"><strong>900+ different instruments</strong></a> from one environment. Its wide range of data acquisition interfaces allows connection to virtually <strong>any chromatograph</strong>. Clarity supports various applications (<strong>PDA</strong>, <strong>MS</strong>, <strong>GPC</strong>, <strong>NGA</strong>, etc.).</p>
<blockquote>
<h5><a href="https://www.dataapex.com/product/clarity-shimadzu-edition-demo?language_content_entity=en&amp;promotion=MKT1625"><strong>Clarity - Shimadzu Edition DEMO version</strong></a></h5>
</blockquote>
<blockquote>
<ul>
<li><strong>Preview</strong> all Clarity - Shimadzu Edition functions</li>
<li>Experience the look and feel of <strong>working</strong> with Clarity - Shimadzu Edition</li>
<li><strong>Data acquisition</strong> simulated from a data file</li>
<li>Demo data for <strong>data processing</strong></li>
<li>All controlled instruments available in demo mode</li>
</ul>
</blockquote>
<p><strong>DataApex</strong> is solely focused on <strong>chromatography software development</strong>. A strong emphasis is placed on technological innovation, visionary adoption of new laboratory standards, best practices, and extensive customer support. DataApex products are sold in <strong>over 100 countries</strong> around the world. Eleven chromatography instrument manufacturers resell privately labeled versions (<strong>OEMs</strong>) of <strong>DataApex’s software</strong>.</p>
<blockquote>
<p><strong>To obtain further information about DataApex Clarity products, please contact us at sales@dataapex.com or visit <a href="https://www.dataapex.com/">www.dataapex.com</a></strong></p>
</blockquote>


Shimadzu Nexera LC-40 HPLC system supported in Clarity

<p><strong>In the next few weeks, the following webinars await you in the field of gas / solid phase and especially GC and GC/MS.</strong></p>
<blockquote>
<h4><a href="https://gcms.labrulez.com/webinars"><strong>👉 DETAILS AND REGISTRATION IN THE WEBINARS SECTION</strong></a></h4>
</blockquote>
<blockquote>
<p><strong>👉 Search and filter</strong> in more than <strong>2 000 GC, LC nad MS webinars</strong>.</p>
</blockquote>
<h5><strong>1. Thermo Fisher Scientific: New GC technology makes your day in the lab simpler and saves helium</strong></h5>
<ul>
<li>Mo, 10.10.2022, 11:00 (CEST)</li>
</ul>
<p>In the webinar, Ms. Gerhards will present improvements to the new GC and GC-MS generation, which were developed with the wishes and suggestions of users in mind. </p>
<h5><strong>2. Shimadzu Corporation: For the Love of Food! - Shimadzu&#39;s GCMS Solutions for the Analysis of Ethylene Oxide</strong></h5>
<ul>
<li>We, 12.10.2022, 08:00 (CEST)</li>
</ul>
<p>Learn about Shimadzu’s GCMS solutions in analyzing ethylene oxide in different food matrices, such as sesame seeds and instant noodles.</p>
<h5><strong>3. Phenomenex: Advances in GC for Environmental Semivolatile and Volatile Organic Analysis</strong></h5>
<ul>
<li>Tu, 18.10.2022, 19:00 (CEST)</li>
</ul>
<p>New technologies in GC that facilitates Semivolatile and volatile analysis,method development tips and tricks and Understand GC column role.</p>
<h5><strong>4. Wiley: Automate GC-MS analysis with KnowItAll MS Expert</strong></h5>
<ul>
<li>Tu, 25.10.2022, 16:00 (CEST)</li>
</ul>
<p>Discover how you can save hours of manual GC-MS analysis time.</p>


Webinars LabRulezGCMS Week 41-43/2022

<h3><strong>Program CEEPC/IPM/CMSC 2022</strong></h3>
<blockquote>
<p><a href="https://lcms.labrulez.com/labrulez-bucket-strapi-h3hsga3/abstractbook_2022_3bec805e4e/abstractbook_2022.pdf"><strong>Complete program including abstracts for download</strong></a></p>
</blockquote>
<p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/CSHS_Konference_CEEPC_IPM_CMSC_2022_2_aa28bf7c17/CSHS-Konference-CEEPC-IPM-CMSC-2022-2.webp" alt="CSMS: Conference CEEPC/IPM/CMSC 2022"/></p>
<h3><strong>Saturday October 1, 2022</strong></h3>
<h4><strong>8:50 - 10:50 Session V – Applications in Biomedicine 2</strong></h4>
<ul>
<li>Chairperson: Haci Mehmet Kayili</li>
</ul>
<h5><strong>8:50-9:10 Proteomic Analysis of Hepatitis B Virus</strong></h5>
<ul>
<li>Martin Hubálek</li>
</ul>
<p>According to the World Health Organisation, an estimated 296 million people worldwide are infected with Hepatitis B virus (HBV). HBV is a small enveloped DNA virus from Hepadnaviridae family that persists in the infected hepatocytes by establishing an episomal covalently closed circular double-stranded DNA (cccDNA) genome containing four open reading frames (C, P, S and X). The ORFs largely overlap and encode multiple proteins using different in-frame start codons. The S ORF encodes three forms of surface envelope glycoproteins S-, M-, and L- HBs). The HBV preC-C gene gives rise to two different products translated from distinct mRNAs – core protein (HBc) and precore protein (HBe). Despite their high sequence similarity, these proteins exhibit different functions and subcellular localizations. The P ORF encodes viral polymerase, and the X ORF encodes regulatory HBx protein.</p>
<p>Mass Spectrometry department of IOCB has established a collaboration with the groups of Iva Pichova and Jan Weber from IOCB. This collaboration on proteomics experiments lead to the discovery of several important biological and biochemical findings including identification of interacting partners of HBc, HBx and HBe proteins or posttranslational modifications of HBc protein. The collaboration resulted in several publications. The proteomic analysis of individually expressed viral proteins has also captured out-of-frame products suggesting the possibility of frameshift or alternative internal initiation of translation. The presentation will highlight the proteomic analyses of HBV at IOCB</p>
<p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/CSHS_Konference_CEEPC_IPM_CMSC_2022_Proteomic_Analysis_of_Hepatitis_B_Virus_Martin_Hubalek_a95dd6216f/CSHS-Konference-CEEPC-IPM-CMSC-2022-Proteomic-Analysis-of-Hepatitis-B-Virus-(Martin-Hubalek).webp" alt="CSMS: Conference CEEPC/IPM/CMSC 2022: Proteomic Analysis of Hepatitis B Virus (Martin Hubálek)"/></p>
<h5><strong>9:10-9:30 The single amino acid substitutions in Mason-Pfizer Monkey Virus matrix protein modulate its proteolytic cleavage rate</strong></h5>
<ul>
<li>Jakub Sýs</li>
</ul>
<p>N-terminal domain of polyprotein Gag of Mason-Pfizer Monkey Virus (M-PMV) Matrix protein (MA) is naturally myristoylated on its N-terminus. When MA is a part of polyprotein Gag, the myristate moiety is buried inside hydrophobic pocket and exposed probably upon interaction with host cell plasma membrane (PM). This mechanism called myristoyl switch does not occur in M-PMV as readily as it does in HIV-1, suggesting that it may have an important role in M-PMV maturation by regulating the MA cleavage from Gag polyprotein.</p>
<p>To address this hypothesis, we have treated the myristoylated (myrMAPPHis) and nonmyristoylated MAPPHis (nonmyrMAPPHis) M PMV construct, bearing the cleavage site for M-PMV viral protease (Pr13), on artificial liposomes mimicking PM by Pr13 for several time points. In contrast to rapidly degraded nonmyrMAPPHis even without liposomes, the myrMAPPHis, surprisingly, become cleaved more frequently only after addition of liposomes indicating the possible exposure of myristate upon interaction with PM.</p>
<p>To support our findings, we have designed and examined also four mutants of MAPPHis M PMV with single amino acid substitutions with expectation to block or, conversely, facilitate the myristoyl switch by stabilization (A79V, A79L) or destabilization (I51A, I86A) of MA M PMV hydrophobic pocket. The mutants A79V and A79L were cleaved even less effectively than myrMAPPHis as well as the degradation of mutants I51A and I86A was faster compared to nonmyrMAPPHis. The different cleavage rates of proteins were confirmed also on structural level by using method of hydrogendeuterium exchange coupled with mass spectrometric detection. It shows that the protease cleavage site has different dynamics in proteins as a result of disruption/stabilisation of hydrophobic pocket.</p>
<p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/CSHS_Konference_CEEPC_IPM_CMSC_2022_The_single_amino_acid_substitutions_in_Mason_Pfizer_Monkey_Virus_matrix_protein_modulate_its_proteolytic_cleavage_rate_Jakub_Sys_e300792938/CSHS-Konference-CEEPC-IPM-CMSC-2022-The-single-amino-acid-substitutions-in-Mason-Pfizer-Monkey-Virus-matrix-protein-modulate-its-proteolytic-cleavage-rate-(Jakub-Sys).webp" alt="CSMS: Conference CEEPC/IPM/CMSC 2022: The single amino acid substitutions in Mason-Pfizer Monkey Virus matrix protein modulate its proteolytic cleavage rate (Jakub Sýs)"/></p>
<h5><strong>9:30-9:50 Cardiac alarmins as residual risk markers of atherosclerosis under lipid-lowering therapy</strong></h5>
<ul>
<li>Viorel-Iulian Suica</li>
</ul>
<p>Background: The major cause in the initiation and progression of atherosclerosis are the high levels of low-density lipoproteins. Although statin treatment can effectively lower these levels, there is still a residual risk of cardiovascular events. We hypothesize that a specific panel of alarmins, a family of stress-sensing molecules, could indicate the persistence of silent atherosclerosis residual risk. </p>
<p>Methods: New Zeeland White rabbits were divided into: the control group (C) with standard diet, a group which received a high-fat diet for 12 weeks (Au) and a treated hyperlipidemic group, with a lipid diet for 8 weeks followed by standard diet and hypolipidemic treatment (atorvastatin and PCSK9 siRNA-inhibitor) for 4 weeks (Asi). We used the LTQ Orbitrap Velos Pro mass spectrometer to analyse the left ventricle lysates. The experiments were complemented by immunologic and genomic assays to corroborate the data.</p>
<p>Results: The hyperlipidemic diet determined a general alarmin up-regulation tendency over C group. A significant spectral abundance increase was measured for specific heat shock proteins, S100 family members, HMGB1 and Annexin A1. The hypolipidemic treatment demonstrated a reversed regulation trend, with non-significant spectral alteration over the C group for some identified alarmins.</p>
<p>Conclusion: Our study highlights the discriminating potential of alarmins in hyperlipidemia or following a hypolipidemic treatment.</p>
<h5><strong>9:50-10:10 Cervical mucus – a non-invasive uterine biomarker source?</strong></h5>
<ul>
<li>Tomáš Oždian</li>
</ul>
<p>Cervical mucus (CM) is a viscous fluid produced by cervical glands located in the myometrium of the uterine cervix. Usually, CM forms a plug between vagina and uterus. During the ovulation, CM starts to be more fluidic to allow the sperm to go through. During the ovulation, there is a good window for non-invasive sampling of the CM, originating from uterine derived tissues. The main hypothesis for CM proteomic study is to develop a method for CM sampling, processing and to answer if there are enough proteins in the CM for potential biomarker search. The resulting protocol consists of mucus dissolution, multi-enzyme digestion, and LC-MS proteomic analysis. The optimized approach allows to identify more than thousand proteins from every sample tested. The bioinformatic analysis reveals that the identified proteins are both intra and extra cellular and discovers the proteins with enriched expression in the broader female reproductive tract. To our best knowledge, we provide the most extensive proteomic characterization available.</p>
<h5><strong>10:10-10:30 High-Throughput µLC-MS/MS Lipidomics of 3D In Vitro Disease Models to Investigate Lipid Dysregulation</strong></h5>
<ul>
<li>Darshak Gadara</li>
</ul>
<p>Microflow liquid chromatography interfaced with mass spectrometry is increasingly applied for the high-throughput profiling of biological samples, as it demonstrated an acceptable tradeoff between sensitivity and reproducibility. However, a limited number of applications developed in lipidomics. This study introduces a robust, sensitive, and high-throughput μLC-MS/MS lipidomics workflow, applied in a differential lipidome study of APOE 3 and 4 phenotypes in iPSC-derived cerebral organoids (CO). First, we optimized the microbore column gradient conditions, injecting a mixture of 15 lipid standards on the UHPLC system coupled to a 6469 QQQ. Our μLC-MS/MS method allows quantitation of 351 lipid species from the single CO. The microflow lipidomics shows an average 3.7-fold increase in response compared to a conventional high-flow method. To benchmark the quantitative performance, 303 samples were acquired over 75 hours. The median coefficient of variation (CV) of 351 lipid species was 12.95%, only 26 lipid species show CV higher than 30%. We demonstrated that microflow separation coupled to three-stage quadruple MS substantially increases the sensitivity and allows for robust multiplexed lipid profiling (including cholesterol determination) in a single cerebral organoid. As a proof of concept, lipidomics analysis was performed for the lipid extract of APOE 3/3 and APOE 4/4 (n=10) CO samples. To our knowledge, this is the first systematic report to demonstrate the microflow LC-MS/MS allows for sensitive, high-throughput, and robust measurement of global lipidome, opening an avenue for routine application of microflow separation in the field of lipidomics.</p>
<p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/CSHS_Konference_CEEPC_IPM_CMSC_2022_High_Throughput_LC_MS_MS_Lipidomics_of_3_D_In_Vitro_Disease_Models_to_Investigate_Lipid_Dysregulation_Darshak_Gadara_0935fe540d/CSHS-Konference-CEEPC-IPM-CMSC-2022-High-Throughput-LC-MS-MS-Lipidomics-of-3D-In-Vitro-Disease-Models-to-Investigate-Lipid-Dysregulation-(Darshak-Gadara).webp" alt="CSMS: Conference CEEPC/IPM/CMSC 2022: High-Throughput µLC-MS-MS Lipidomics of 3D In Vitro Disease Models to Investigate Lipid Dysregulation (Darshak Gadara)"/></p>
<h5><strong>10:30-10:50 Multi-omics network analysis in atherosclerosis reveals mechanisms driving the progression towords complicated lesion</strong></h5>
<ul>
<li>Eva Csosz</li>
</ul>
<p>From a biological point of view, it is crucial to understand the mechanisms laying behind atherosclerosis and its complicated forms. In the process of atherosclerosis, first, an atheromatous plaque builds up, which in some conditions can lead to the appearance of complicated lesions. The complicated lesion is characterized by ruptures on the atherosclerotic plaque surface and/or hemorrhage into the plaque. According to the WHO, hemorrhaged lesions, contribute to a considerable extent of deaths worldwide.</p>
<p>The main goal of our project was to perform a multi-omics study involving transcriptomics and proteomics data to get more insights into the pathophysiological processes dominating the complicated lesions.</p>
<p>Transcriptomic (RNAseq) and proteomic (label-free quantification) data were obtained by the analysis of artery samples originating from healthy arteries, atheromatous lesions, and complicated lesions. Both data types were examined separately by Ingenuity Pathway Analysis and later an overlay of the networks was achieved.</p>
<p>120 differentially expressed (DE) proteins and more than 4000 DE genes were detected. The deep analysis of the data could identify the proteins and transcripts characteristic of the complicated lesions and could reveal the pathways specific to atheroma and complicated lesions, respectively. The DE genes were arranged into 25 networks, while the DE proteins were into 12 networks. The lower number of DE proteins compared to the number of DE genes did not result in loss of information, indicating the power of the proteomics experiments. In spite of providing a lower number of DE items, the biological information achievable from proteomics experiments has equal value compared to transcriptomics data.</p>
<p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/CSHS_Konference_CEEPC_IPM_CMSC_2022_Multi_omics_network_analysis_in_atherosclerosis_reveals_mechanisms_driving_the_progression_towords_complicated_lesion_Eva_Csosz_aa54a2b04f/CSHS-Konference-CEEPC-IPM-CMSC-2022-Multi-omics-network-analysis-in-atherosclerosis-reveals-mechanisms-driving-the-progression-towords-complicated-lesion-(Eva-Csosz).webp" alt="CSMS: Conference CEEPC/IPM/CMSC 2022: Multi-omics network analysis in atherosclerosis reveals mechanisms driving the progression towords complicated lesion (Eva Csosz)"/></p>
<h5><strong>10:50 - 11:10 Coffee break</strong></h5>
<h4><strong>11:10 - 12:00 Plenary lecture III:: Light-mediated discovery of surfaceome nanoscale organization and inter-cellular receptor interaction networks</strong> (Chairperson: Pavel Bouchal)</h4>
<ul>
<li>Bernd Wollscheid</li>
</ul>
<p>The molecular nanoscale organization of the surfaceome is a fundamental regulator of cellular signaling in health and disease. Technologies for mapping the spatial relationships of cell surface receptors and their extracellular signaling synapses would unlock theranostic opportunities to target protein communities and the possibility to engineer extracellular signaling. Here, we develop an optoproteomic technology termed LUX-MS that enables the targeted elucidation of acute protein interactions on and in between living cells using light-controlled singlet oxygen generators (SOG). By using SOG-coupled antibodies, small molecule drugs, biologics and intact viral particles, we demonstrate the ability of LUX-MS to decode ligand receptor interactions across organisms and to discover surfaceome receptor nanoscale organization with direct implications for drug action. Furthermore, by coupling SOG to antigens we achieved light-controlled molecular mapping of intercellular signaling within functional immune synapses between antigen-presenting cells and CD8⁺ T cells providing insights into T cell activation with spatiotemporal specificity. LUX-MS based decoding of surfaceome signaling architectures thereby provides a molecular framework for the rational development of theranostic strategies.</p>
<p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/CSHS_Konference_CEEPC_IPM_CMSC_2022_Light_mediated_discovery_of_surfaceome_nanoscale_organization_and_inter_cellular_receptor_interaction_networks_Bernd_Wollscheid_019214ab5c/CSHS-Konference-CEEPC-IPM-CMSC-2022-Light-mediated-discovery-of-surfaceome-nanoscale-organization-and-inter-cellular-receptor-interaction-networks-(Bernd-Wollscheid).webp" alt="CSMS: Conference CEEPC/IPM/CMSC 2022: Light-mediated discovery of surfaceome nanoscale organization and inter-cellular receptor interaction networks (Bernd Wollscheid)"/></p>
<h4><strong>12:00 - 12:20 Poster prize, Closing remarks</strong></h4>
<p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/CSHS_Predavani_oceneni_konference_CEEPC_IPM_CMSC_2022_Ales_Kvasnicka_a_Michael_Volny_4c0967dd3b/CSHS-Predavani-oceneni-konference-CEEPC-IPM-CMSC-2022-(Ales-Kvasnicka-a-Michael-Volny).webp" alt="ČSHS: Conference prize CEEPC/IPM/CMSC 2022 (Aleš Kvasnička a Michael Volný)"/></p>
<p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/CSHS_Eu_PA_cestovni_granty_Nejlepsi_kratke_sdeleni_Kalaninova_Zuzana_a_Eva_Csosz_ef6a262eae/CSHS-EuPA-cestovni-granty-Nejlepsi-kratke-sdeleni-(Kalaninova-Zuzana-a-Eva-Csosz).webp" alt="ČSHS: EuPA travel grants: Short talk prize CEEPC/IPM/CMSC 2022 (Kalaninová Zuzana a Eva Csosz)"/></p>
<p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/CSHS_Vyhlaseni_nejlepsiho_posteru_Konference_CEEPC_IPM_CMSC_2022_Anton_Skriba_a_Michael_Volny_0010fccaaa/CSHS-Vyhlaseni-nejlepsiho-posteru-Konference-CEEPC-IPM-CMSC-2022-(Anton-Skriba-a-Michael-Volny).webp" alt="ČSHS: Poster prize CEEPC/IPM/CMSC 2022 (Anton Škríba a Michael Volný)"/></p>
<p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/CSHS_Eu_PA_cestovni_granty_Nejlepsi_poster_Jadeja_Siddharth_a_Eva_Csosz_dac2e7c761/CSHS-EuPA-cestovni-granty-Nejlepsi-poster-(Jadeja-Siddharth-a-Eva-Csosz).webp" alt="ČSHS: EuPA travel grants: Poster prize CEEPC/IPM/CMSC 2022 (Jadeja Siddharth a Eva Csosz)"/></p>
<h5><strong>12:20 - 13:30 Lunch</strong></h5>
<p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/CSHS_Konference_CEEPC_IPM_CMSC_2022_Obcerstveni_44ad451fcc/CSHS-Konference-CEEPC-IPM-CMSC-2022-Obcerstveni.webp" alt="CSMS: Conference CEEPC/IPM/CMSC 2022: Coffe break"/></p>


Conference CEEPC/IPM/CMSC 2022 (Day 3)

<p><strong>STARSS project is approaching its end after more than five years. A few more months remain before it will be concluded. The major objective of the project was to create a strong team of researchers enabling significant progress in the field of the separation science. The annual STARSS conferences have always been a good opportunity to bring people from several Czech and European institutions in Hradec Kralove where we have met face to face for a few days in order to inform each other about the progress in the research. It is clear that the focus of these conferences has been on the exchange in scientific information. However, an integral part of our previous conferences has also included informal meetings when we had time to talk about issues sometimes even completely outside of science perhaps with a drink and food. Social part of conferences is simply indispensable.</strong></p>
<p><strong>I trust that this conference will be at least as interesting as all the previous ones. Its program is rich and includes presentations by renowned “icons” of separation science from both abroad and the Czech Republic, as well as talks given by students and postdocs. Such “cross-pollination” will certainly be uplifting for all involved. I wish all those who attend this conference a pleasant stay in Hradec Králové and enjoyable conferencing.</strong></p>
<p><strong><a href="https://lcms.cz/articles?search=Franti%C5%A1ek+%C5%A0vec">Prof. František Švec</a></strong></p>
<h3><strong>Program: 6th STARSS Conference on Separation Science</strong></h3>
<ul>
<li><a href="https://portal.faf.cuni.cz/getattachment/Projects/STARSS/Events/6th-STARSS-conference/Program/2022-STARSS-booklet.pdf.aspx?lang=en-GB"><strong>Conference booklet including speakers bio</strong></a></li>
</ul>
<h3><strong>DAY 1: Monday 17. 10. 2022</strong></h3>
<h5><strong>08:00 – 09:00 REGISTRATION</strong></h5>
<h5><strong>09:00 – 09:20 Welcoming address</strong></h5>
<ul>
<li>Prof. Petr Solich, Prof. František Švec, Prof. Lucie Nováková</li>
<li>Assoc. Prof. Jaroslav Roh (the dean of the Faculty of Pharmacy, Faculty of Pharmacy, Charles University, Hradec Králové, Czech Republic)</li>
</ul>
<h4><strong>SESSION I: IMPORTANCE OF SEPARATION SCIENCE FOR CLINICAL APPLICATIONS</strong></h4>
<ul>
<li>Chairperson: Prof. František Švec</li>
</ul>
<h5><strong>09:20 – 10:00 L-01: UHPSFC/MS as a powerful tool for high-throughput lipidomic quantitation in cancer screening</strong></h5>
<ul>
<li><a href="https://lcms.cz/articles?search=Michal+Hol%C4%8Dapek">Prof. Michal Holčapek</a> (University of Pardubice, Czech Republic)</li>
</ul>
<h5><strong>10:00 – 10:40 L-02: Selected ion flow tube mass spectrometry, SIFT-MS, analyses of volatile metabolites in exhaled breath</strong></h5>
<ul>
<li>Prof. Patrik Španěl (J. Heyrovský Institute of Physical Chemistry, Prague, Czech Republic)</li>
</ul>
<h5><strong>10:40 – 11:10 Coffee-break and discussion</strong></h5>
<h4><strong>SESSION II: BIOPHARMACEUTICALS</strong></h4>
<ul>
<li>Chairperson: Prof. Lucie Nováková</li>
</ul>
<h5><strong>11:10 – 11:50 L-03: Simplifying the characterization of complex biopharmaceutical products through the use of ultra-short columns or multi-isocratic elution mode</strong></h5>
<ul>
<li>Dr. Davy Guillarme (University of Geneva, Switzerland)</li>
</ul>
<h5><strong>11:50 – 12:20 L-04: Analysis of therapeutic proteins by multidimensional LC: How far can we go?</strong></h5>
<ul>
<li>Dr. Valentina D ́Atri (University of Geneva, Switzerland)</li>
</ul>
<h5><strong>12:20 – 12:40 L-05: pyroLC: online thermal decomposition of proteins as a tool for ultra-fast bottom-up proteomics</strong></h5>
<ul>
<li>Dr. Juraj Lenčo (Charles University, Hradec Králové, Czech Republic)</li>
</ul>
<h5><strong>12:40 – 13:00 L-06: RPLC-UV and HILIC-UV characterization of home-made ramucirumab-based antibody-drug conjugate</strong></h5>
<ul>
<li>Denis Naplekov (Charles University, Hradec Králové, Czech Republic)</li>
</ul>
<h5><strong>13:00 – 14:00 Lunch</strong></h5>
<h4><strong>SESSION III: 2D SEPARATIONS</strong></h4>
<ul>
<li>Chairperson: Assoc. Prof. Jiří Urban</li>
</ul>
<h5><strong>14:00 – 14:40 L-07: What can we expect from LC x LC compared to conventional 1D-LC</strong></h5>
<ul>
<li>Prof. Sabine Heinisch (Université Claude Bernard Lyon 1, Lyon, France)</li>
</ul>
<h5><strong>14:40 – 15:20 L-08: Modelling of analyte profiles and band broadening generated by interface loops used in multi-dimensional liquid chromatography</strong></h5>
<ul>
<li>Prof. Ken Broeckhoven (Vrije Universiteit Brussel, Belgium)</li>
</ul>
<h5><strong>15:20 – 15:50 L-09: Off-line LC x SFC in the prospect of upgrading natural or recycled products</strong></h5>
<ul>
<li>Dr. Karine Faure (Université Claude Bernard Lyon 1, Lyon, France)</li>
</ul>
<h5><strong>15:50 – 16:20 L-10: Two-dimensional liquid chromatographic separations of complex samples of industrial products and intermediates</strong></h5>
<ul>
<li><a href="https://lcms.cz/articles?search=Petr+%C4%8Cesla"><strong>Assoc. Prof. Petr Česla</strong></a> (University of Pardubice, Czech Republic)</li>
</ul>
<h5><strong>16:20 – 16:50 Coffee-break and discussion</strong></h5>
<h4><strong>SESSION IV: IMPORTANCE OF STEROIDS</strong></h4>
<ul>
<li>Chairperson: Prof. Marcela Segundo</li>
</ul>
<h5><strong>16:50 – 17:30 L-11: An image of the future of steroid biochemistry</strong></h5>
<ul>
<li>Prof. Ruth Andrew (University of Edinburgh, UK)</li>
</ul>
<h5><strong>17:30 – 18:00 L-12: Ecdysterone metabolism: A holistic view on compound identification for doping control</strong></h5>
<ul>
<li>Prof. Maria Kristina Parr (Freie Universität Berlin, Berlin, Germany)</li>
</ul>
<h5><strong>18:00 – 18:30 L-13: New liquid chromatography-tandem mass spectrometry method for targeted profiling of steroids in mouse plasma</strong></h5>
<ul>
<li>Taťána Gazárková (Charles University, Hradec Králové, Czech Republic)</li>
</ul>
<h5><strong>18:30 – 19:30 Welcome drink</strong></h5>
<h3><strong>DAY 2: Tuesday 18. 10. 2022</strong></h3>
<h5><strong>08:00 – 09:00 REGISTRATION</strong></h5>
<h4><strong>SESSION V: SUPERCRITICAL FLUID CHROMATOGRAPHY AND EXTRACTIONS</strong></h4>
<ul>
<li>Chairperson: Assoc. Prof. Radim Kučera</li>
</ul>
<h5><strong>09:00 – 09:30 L-14: Supercritical fluid extraction and chromatography in life science applications</strong></h5>
<ul>
<li>Prof. Charlotta Turner (Lund University, Lund, Sweden)</li>
</ul>
<h5><strong>09:30 – 10:00 L-15: Supercritical fluid chromatography – tandem mass spectrometry for analysis of vitamin D metabolites in biological samples</strong></h5>
<ul>
<li>Dr. Margareta Sandahl (Lund University, Lund, Sweden)</li>
</ul>
<h5><strong>10:00 – 10:30 L-16: The effect of make-up solvent composition on responses in SFC-MS: Electrospray vs UniSpray</strong></h5>
<ul>
<li>Dr. Kateřina Plachká (Charles University, Hradec Králové, Czech Republic)</li>
</ul>
<h5><strong>10:30 – 11:00 L-17: UHPSFC-MS/MS versus 2D-UHPLC-MS/MS in chiral separation of Propranolol and its Hydroxy Metabolites</strong></h5>
<ul>
<li>Lukas Harps (Freie Universität Berlin, Berlin, Germany)</li>
</ul>
<h5><strong>11:00 – 11:30 Coffee-break and discussion</strong></h5>
<h4><strong>SESSION VI: COLUMN TECHNOLOGY</strong></h4>
<ul>
<li>Chairperson: Prof. Dalibor Šatínský</li>
</ul>
<h5><strong>11:30 – 12:10 L-18: Hypercrosslinked monolithic stationary phases in proteomics</strong></h5>
<ul>
<li>Assoc. Prof. Jiří Urban (Masaryk University, Brno, Czech Republic)</li>
</ul>
<h5><strong>12:10 – 12:40 L-19: Guidelines for tuning the macropore structure of monolithic columns for high-performance liquid chromatography</strong></h5>
<ul>
<li>Dr. Sebastiaan Eeltink (Vrije Universiteit Brussel, Belgium)</li>
</ul>
<h5><strong>12:40 – 13:10 L-20: Strategies and chemistry in column development</strong></h5>
<ul>
<li>Assoc. Prof. Michal Kohout (University of Chemistry and Technology, Prague, Czech Republic)</li>
</ul>
<h5><strong>13:10 – 14:30 Lunch</strong></h5>
<h4><strong>SESSION VII: RETENTION MECHANISMS AND STATIONARY PHASES</strong></h4>
<ul>
<li>Chairperson: Prof. Spas Kolev</li>
</ul>
<h5><strong>14:30 – 15:00 L-21: Understanding the mechanism, advantages and limitations of hydrophilic interaction liquid chromatography</strong></h5>
<ul>
<li>Prof. David McCalley (University of West England, UK)</li>
</ul>
<h5><strong>15:00 – 15:30 L-22: Study of molecular structures through retention mechanisms in liquid chromatography: New trends and applications</strong></h5>
<ul>
<li>Dr. Jean-Christophe Garrigues (Paul Sabatier University - Toulouse III, Toulouse, France)</li>
</ul>
<h5><strong>15:30 – 16:00 L-23: Problems of stationary phases in SFC</strong></h5>
<ul>
<li>Prof. Lucie Nováková (Charles University, Hradec Králové, Czech Republic)</li>
</ul>
<h5><strong>16:00 – 16:30 L-24: The chromatographic behaviour of pharmaceuticals on stationary phases based on metal oxides</strong></h5>
<ul>
<li>Assoc. Prof. Radim Kučera (Charles University, Hradec Králové, Czech Republic)</li>
</ul>
<h5><strong>16:30 – 17:00 Coffee-break and discussion</strong></h5>
<h4><strong>SESSION VIII: SAMPLE PREPARATION AND APPLICATIONS</strong></h4>
<ul>
<li>Chairperson: Assoc. Prof. Hana Sklenářová</li>
</ul>
<h5><strong>17:00 – 17:30 L-25: Glucosinolate profiling in Brassicaceae family: instrumental analysis and biological application</strong></h5>
<ul>
<li>Dr. Iva Pavlovic (Palacký University, Olomouc, Czech Republic)</li>
</ul>
<h5><strong>17:30 – 18:00 L-26: Flow programming for the development of online solid-phase extraction</strong></h5>
<ul>
<li>Assoc. Prof. Petr Chocholouš (Charles University, Hradec Králové, Czech Republic)</li>
</ul>
<h5><strong>18:00 – 18:30 L-27: Automated tandem homogeneous liquid-liquid extraction and centrifugation-less deproteination for complex sample analysis on HPLC</strong></h5>
<ul>
<li>Dr. Burkhard Horstkotte (Charles University, Hradec Králové, Czech Republic)</li>
</ul>
<h5><strong>19:00 – 22:00 Conference dinner</strong></h5>
<h3><strong>DAY 3: Wednesday 19. 10. 2022</strong></h3>
<h4><strong>WORKSHOPS: FACULTY OF PHARMACY</strong></h4>
<h5><strong>08:00 – 10:30 W1: Supercritical fluid extraction of polar and nonpolar compounds from Eucalyptus sp.</strong></h5>
<ul>
<li>Laboratory 916, 8th floor, Faculty of Pharmacy</li>
<li>Dr. Veronika Pilařová (Charles University, Hradec Králové, Czech Republic)</li>
</ul>
<h5><strong>08:00 – 10:30 W2: MetAmino® Kit – simple and easy sample preparation method for your LC-MC or GC-MS analysis</strong></h5>
<ul>
<li>Student’s Laboratory, 3rd floor, Faculty of Pharmacy</li>
<li>Ing. Jana Volková (Chromservis, Czech Republic)</li>
</ul>
<h5><strong>10:30 – 11:00 Coffee-break and discussion</strong></h5>
<h5><strong>11:00 – 13:30 W3: Who will help you with sample prep and liquid handling?</strong></h5>
<ul>
<li>Student’s Laboratory, 4th floor, Faculty of Pharmacy</li>
<li>Dr. Martina Riesová (<a href="https://lcms.cz/companies/50"><strong>Waters</strong></a>, Prague, Czech Republic)</li>
</ul>
<h5><strong>13:30 – 14:30 Lunch</strong></h5>
<h5><strong>14:30 – 17:00 W4: Practical application of nanofibers for advanced extraction approaches in chromatography</strong></h5>
<ul>
<li>Student’s Laboratory no. 524, 4th floor, Faculty of Pharmacy</li>
<li>Prof. Dalibor Šatínský, Dr. Ivona Lhotská (Charles University, Hradec Králové, Czech Republic)</li>
</ul>
<h5><strong>17:00 – 18:00 Coffee-break and discussion</strong></h5>


6th STARSS Conference on Separation Science (Program)

<p><strong>In the  week from October 17 &amp; 24 , 2022, the following webinars await you in the field of gas / solid phase and especially GC and GC/MS.</strong></p>
<blockquote>
<h4><a href="https://gcms.labrulez.com/webinars"><strong>👉 DETAILS AND REGISTRATION IN THE WEBINARS SECTION</strong></a></h4>
</blockquote>
<blockquote>
<p><strong>👉 Search and filter</strong> in more than <strong>2 000 GC, LC nad MS webinars</strong>.</p>
</blockquote>
<h5><strong>1. Agilent Technologies: A Discussion on the Theory of IR Spectroscopy</strong></h5>
<ul>
<li>Mo, 17.10.2022, 21:30 (CEST)</li>
</ul>
<p>This session will focus on the theory of Infrared and will discuss some modern infrared analytical techniques.</p>
<h5><strong>2. Phenomenex: Advances in GC for Environmental Semivolatile and Volatile Organic Analysis</strong></h5>
<ul>
<li>Tu, 18.10.2022, 19:00 (CEST)</li>
</ul>
<p>New technologies in GC that facilitates Semivolatile and volatile analysis,method development tips and tricks and Understand GC column role.</p>
<h5><strong>3. Waters Corporation: APGC-MS/MS a game changer for routine pesticide analysis: Reaching new heights</strong></h5>
<ul>
<li>Th, 20.10.2022, 11:00 (CEST)</li>
</ul>
<p>The use of GC-MS/MS utilizing APGC has been shown to offer significant improvements in performance over electron ionization (EI) for pesticide residue analysis, in terms of selectivity and specificity.</p>
<h5><strong>4. Agilent Technologies: MicroLab Software introduction for Agilent FTIR systems</strong></h5>
<ul>
<li>Th, 20.10.2022, 20:00 (CEST)</li>
</ul>
<p>This online seminar provides a comprehensive introduction to Agilent FTIR spectrometers and MicroLab software to help customers from Academic F15Teaching Labs to facilitate their operation.</p>
<h5><strong>5. Agilent Technologies: Meet a Versatile Agilent Cary 630 FTIR</strong></h5>
<ul>
<li>Mo, 24.10.2022, 21:30 (CEST)</li>
</ul>
<p>Developing models for FTIR quantitative analysis is simple using Agilent Cary 630 FTIR spectrometers and MicroLab FTIR software.</p>
<h5><strong>6. ACD/Labs: What&#39;s That Peak? Structure Elucidation &amp; Verification Virtual Symposium (Day 1)</strong></h5>
<ul>
<li>Tu, 25.10.2022, 15:30 (CEST)</li>
</ul>
<p>What’s in my sample? Did I make what I think I made? What’s that peak?</p>
<h5><strong>7. Wiley: Automate GC-MS analysis with KnowItAll MS Expert</strong></h5>
<ul>
<li>Tu, 25.10.2022, 16:00 (CEST)</li>
</ul>
<p>Discover how you can save hours of manual GC-MS analysis time.</p>
<h5><strong>8. ACD/Labs: What&#39;s That Peak? Structure Elucidation &amp; Verification Virtual Symposium (Day 2)</strong></h5>
<ul>
<li>We, 26.10.2022, 15:30 (CEST)</li>
</ul>
<p>What’s in my sample? Did I make what I think I made? What’s that peak?</p>
<h5><strong>9. Quantum Analytics/Bruker: Polymer Science A to Z: Getting Answers from FTIR and Raman Analyses</strong></h5>
<ul>
<li>We, 26.10.2022, 20:00 (CEST)</li>
</ul>
<p>Let’s tackle the science of polymer analysis using the power of spectroscopy, including identification, quality control and reverse engineering.</p>


Webinars LabRulezGCMS Week 42-43/2022

<p><strong>The Clarity MS Extension is a tool that is used for processing data that has been acquired from selected Mass Spectrometry detectors. Spectral data, together with chromatograms, add a third dimension to analytical data analysis.</strong></p>
<ul>
<li><p>👌 <strong>Combination of MS signals</strong> with conventional GC/HPLC detectors</p>
</li>
<li><p>🔝 MS detectors can be used <strong>in combination with 1000+ instruments</strong> supported in Clarity</p>
</li>
<li><p>💡 MS manufacturers can develop <strong>a driver for their own detectors</strong> using a Clarity Software Development Kit (SDK)</p>
</li>
</ul>
<p><strong>The MS Extension</strong> expands the capability of <strong>Clarity</strong> and <strong>Clarity Offline Chromatography software</strong> by providing interactive spectral analysis, peak purity analysis, and compound identification that is based on a spectral library search. The extension is prepared to function with <strong>single quadrupole MS detectors</strong> and <strong>TOF MS detectors</strong>.</p>
<p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Data_Apex_Clarity_software_Mass_Spectrometry_Extension_1_7fb5562dc3/DataApex-Clarity-software-Mass-Spectrometry-Extension-1.webp" alt="DataApex: Clarity software - Mass Spectrometry Extension"/></p>
<p>All <strong>data is saved in a single file</strong>; a chromatogram at any m/z value or even only a spectrum can simply be recalled for review after an analysis. <strong>MS spectra</strong>, acquired using an MS detector, may be interactively selected <strong>from a chromatogram signal</strong> for visual inspection and comparison. The spectra may also be used for <strong>peak purity determinations</strong> and <strong>component identification</strong> through spectral libraries.</p>
<p>It is possible to import MS data in <strong>AIA</strong> (cdf), <strong>mzXML</strong>, <strong>MzML</strong>, and <strong>mzData</strong> formats.</p>
<p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Data_Apex_Clarity_software_Mass_Spectrometry_Extension_2_6b036064d3/DataApex-Clarity-software-Mass-Spectrometry-Extension-2.webp" alt="DataApex: Clarity software - Mass Spectrometry Extension"/></p>
<p>Control modules for selected detectors (see list of <a href="https://www.dataapex.com/controls"><strong>control modules</strong></a>) are available in Clarity.</p>
<p><strong>Additional control modules for MS detectors can be developed upon request</strong>, please <a href="https://www.dataapex.com/document/contacts"><strong>contact us</strong></a> for availability.</p>
<blockquote>
<h3><strong>Selected supported GC/MS &amp; LC/MS detectors</strong></h3>
</blockquote>
<blockquote>
<h5><strong>LC-MS Detectors</strong></h5>
<ul>
<li><strong>Advion:</strong> Expression</li>
<li><strong>Gilson:</strong> Verity 1920</li>
<li><strong>Konik:</strong> Q4 LCMS</li>
<li><strong>Microsaic:</strong> 4000 MiD</li>
<li><strong>Microsaic:</strong> 4500 MiD</li>
<li><strong>Young In Chromass:</strong> YL9900</li>
</ul>
</blockquote>
<blockquote>
<h5><strong>GC-MS Detectors</strong></h5>
<ul>
<li><strong>Young In Chromass:</strong> ChroZen GC/MS</li>
<li><strong>Young In Chromass:</strong> YL6900</li>
</ul>
</blockquote>
<blockquote>
<h5><strong>GC-MS TOF Detectors</strong></h5>
<ul>
<li><strong>Markes International:</strong> BenchTOF</li>
</ul>
</blockquote>


Clarity software - Mass Spectrometry Extension

ESAS-CSSC 2022 (Day 3)

<p><strong>In the  week from October 24 , 2022, the following webinars await you in the field of gas / solid phase and especially GC and GC/MS.</strong></p>
<blockquote>
<h4><a href="https://gcms.labrulez.com/webinars"><strong>👉 DETAILS AND REGISTRATION IN THE WEBINARS SECTION</strong></a></h4>
</blockquote>
<blockquote>
<p><strong>👉 Search and filter</strong> in more than <strong>2 000 GC, LC nad MS webinars</strong>.</p>
</blockquote>
<h5><strong>1. Agilent Technologies: Meet a Versatile Agilent Cary 630 FTIR</strong></h5>
<ul>
<li>Mo, 24.10.2022, 21:30 (CEST)</li>
</ul>
<p>Developing models for FTIR quantitative analysis is simple using Agilent Cary 630 FTIR spectrometers and MicroLab FTIR software.</p>
<h5><strong>2. ACD/Labs: What&#39;s That Peak? Structure Elucidation &amp; Verification Virtual Symposium (Day 1)</strong></h5>
<ul>
<li>Tu, 25.10.2022, 15:30 (CEST)</li>
</ul>
<p>What’s in my sample? Did I make what I think I made? What’s that peak?</p>
<h5><strong>3. Wiley: Automate GC-MS analysis with KnowItAll MS Expert</strong></h5>
<ul>
<li>Tu, 25.10.2022, 16:00 (CEST)</li>
</ul>
<p>Discover how you can save hours of manual GC-MS analysis time.</p>
<h5><strong>4. Thermo Fisher Scientific: Walkaway sample-to-vial sample preparation with the EXTREVA ASE system</strong></h5>
<ul>
<li>We, 26.10.2022, 09:00 (CEST)</li>
</ul>
<p>Discover the Thermo Scientific EXTREVA ASE Accelerated Solvent Extractor which boosts sample prep productivity, and efficiency, and brings a new level of consistency.</p>
<h5><strong>5. ACD/Labs: What&#39;s That Peak? Structure Elucidation &amp; Verification Virtual Symposium (Day 2)</strong></h5>
<ul>
<li>We, 26.10.2022, 15:30 (CEST)</li>
</ul>
<p>What’s in my sample? Did I make what I think I made? What’s that peak?</p>
<h5><strong>6. Quantum Analytics/Bruker: Polymer Science A to Z: Getting Answers from FTIR and Raman Analyses</strong></h5>
<ul>
<li>We, 26.10.2022, 20:00 (CEST)</li>
</ul>
<p>Let’s tackle the science of polymer analysis using the power of spectroscopy, including identification, quality control and reverse engineering. </p>
<h5><strong>7. Petro Industry News/Metrohm: Making your quality control of hydraulic and lube oils more efficient</strong></h5>
<ul>
<li>Th, 27.10.2022, 14:00 (CEST)</li>
</ul>
<p>Combining titration and Vis-Near-Infrared Spectroscopy for higher sample throughput &amp; faster results.</p>


Webinars LabRulezGCMS Week 43/2022

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Since 1991 DataApex develops and manufactures chromatography data stations. DataApex is constantly striving to provide users with efficient and up-to-date tools for chromatography data processing.

DataApex

The Faculty of Pharmacy, with its seat in the town of Hradec Králové, was established by a government decree in 1969. This Faculty of Pharmacy has continued in the old and long-time tradition of the education of pharmacy at Charles University.

Faculty of Pharmacy, Charles University

is the international joint scientific meeting to share recent developments, exchange ideas, explore new directions and initiate a possible collaboration in the analytical spectrometry area.

ESAS

The relatively new tradition of the Czech mass spectrometry conferences was established only in 2011, the very first event took place in Hradec Králové. Since then, the conference was organized every year except for 2020, the year of the pandemic.

Czech Mass Spectrometry Conferences

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Webinars LabRulezGCMS Week 43/2022

ESAS-CSSC 2022 (Day 3)

Clarity software - Mass Spectrometry Extension

Webinars LabRulezGCMS Week 42-43/2022

6th STARSS Conference on Separation Science (Program)

Conference CEEPC/IPM/CMSC 2022 (Day 3)

Webinars LabRulezGCMS Week 41-43/2022

Shimadzu Nexera LC-40 HPLC system supported in Clarity

Conference CEEPC/IPM/CMSC 2022 (Day 2)

Webinars LabRulezGCMS Week 40/2022

Upcoming events

US HUPO 2026

Thermo Fisher Scientific at US HUPO 2026

Pittcon 2026

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Real-Time In-Line Insight for Therapeutic Protein Production

Microplastics in Wastewater: A Population Based Approach to Identifying Potential Sources

PFAS in Air: A Practical Toolkit for Real-world Applications