<div><div><p><strong>Assoc. Prof. Jan Heyda from the Department of Physical Chemistry at UCT Prague leads the theoretical part of the project “Membraneless Organelles in Biological Environments”. His group uses molecular dynamics simulations to explore how intrinsically disordered proteins form condensates in cells. Together with Assoc. Prof. M. Vazdar, they systematically study the effects of ions, point mutations in proteins, and membrane composition on the formation, stability, and adsorption of these structures at the atomic level. The goal is to create a predictive map that will lead to better understanding of neurodegenerative diseases and development of smart biomaterials, in close collaboration with experiments by Professor Paul Cremer from Pennsylvania State University.</strong></p></div><div><h5><strong>What is your project about and what are your objectives?</strong></h5><p>Our project investigates how so-called membraneless organelles (MLOs) arise and function within cells. These are dynamic structures in which the cell temporarily concentrates selected proteins and RNA so that certain processes can proceed more rapidly and efficiently than in the surrounding environment. Unlike classical organelles, such as mitochondria or the nucleus, they are not bounded by a membrane, but arise through the self-organization of biomolecules into a denser phase — a so-called condensate.</p><p>In the project, we focus mainly on intrinsically <strong>disordered proteins </strong>that have the ability to form these condensates, but are also very sensitive to the composition of the solution, small changes in their sequence, and contact with biological membranes. The goal is to understand, at the molecular level, what controls the transition from freely dispersed molecules to a&nbsp;condensed state and when such a&nbsp;state is still functional or may already lead to pathological behaviour.</p><h5><strong>If the project is successful, what will it bring? How will it help in the fields of medicine or pharmacy?</strong></h5><p>This is still a&nbsp;basic research project, so its<strong> main contribution will be a&nbsp;deeper understanding of the behaviour of proteins in the biological environment</strong>. Such knowledge is important for research into neurodegenerative diseases, where certain proteins lose their native behaviour, but also generally for protein biophysics and the development of biomaterials or biotechnological applications. This is not a&nbsp;project that would immediately lead to new treatments, but it can contribute to ensuring that future, more targeted interventions are on a&nbsp;firmer scientific basis.</p><h5><strong>You lead the theoretical part. What is the nature of the experiments?</strong></h5><p>The experimental part takes place in<strong> Professor Paul Cremer’s&nbsp;group&nbsp;at Pennsylvania State University</strong>. His team prepares the polypeptides under study and monitors their behaviour in the presence of salts at various concentrations and/or on membrane surfaces. Using spectroscopic and thermodynamic methods, they determine under what conditions the condensates form, what their composition is, and how stable they are. The advantage of the project is that the experiments and simulations are designed from the outset to describe the same systems.</p><h5><strong>How did you get involved with the Cremer Group at Pennsylvania State University?</strong></h5><p>During my doctoral studies with <strong>Professor Pavel Jungwirth</strong>, I&nbsp;studied how the presence of ions affects the behaviour of biomolecules.<strong> Professor Cremer </strong>is one of the most prominent figures in this field, and our professional contact gradually developed into a&nbsp;long-term collaboration between experiment and theory. Within the framework of ion-specific effects, we moved from polymers and peptides toward the question of how protein condensates and membraneless organelles can be influenced.</p><h5><strong>How do&nbsp;the experiments differ from the simulations?</strong></h5><p>An experiment shows the overall behaviour of a&nbsp;system, but we often cannot directly discern the underlying molecular causes from it. Simulation allows us to look inside and observe which specific molecular interactions lead to this behaviour. In the experiment, thus, we see the result; in the simulation, its details. Each approach has its limits, but it is their combination that allows us to obtain a&nbsp;much more compelling and comprehensive picture than if we used only one of them.</p></div><p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/VSCHT_Praha_Jan_Heyda_Molekularni_pohled_na_bezmembranove_organely_ve_spolupraci_s_USA_0e39e1232d.jpg" alt="VŠCHT Prague: Jan Heyda: Molecular view of membraneless organelles in collaboration with the USA" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_VSCHT_Praha_Jan_Heyda_Molekularni_pohled_na_bezmembranove_organely_ve_spolupraci_s_USA_0e39e1232d.jpg 245w," sizes="100vw" width="1500" height="898"></p><h5><strong>How does the collaboration between the theorist and the experimenter proceed?</strong></h5><p>In the beginning, it is mostly about finding a&nbsp;common language, especially regarding complex topics. The theorist and the experimentalist view the same problem differently, and it takes some time for both to clarify what is realistic for the other. Once this is achieved, a&nbsp;truly strong collaboration begins to emerge: the experiment helps to anchor the simulations in reality, and the simulations, in turn, provide the experiments with a&nbsp;detailed, physically grounded molecular interpretation.</p><h5><strong>How did you get into physical chemistry and computer modelling?</strong></h5><p>I graduated from a <strong>mathematics-oriented high school in České Budějovice</strong> and enjoyed chemistry, mathematics and physics, so studying physical chemistry was a natural choice for me. I then came to computer simulations through statistical thermodynamics, when I realized that there were few problems that could be solved analytically. On the contrary, computer simulations allow us to assemble even very complicated systems, study them at a microscopic level, and arrive at a mechanistic understanding of key processes. I still enjoy that very much.</p><h5><strong>What shaped you into the scientist you are today?</strong></h5><p>Three things were crucial for me: the supportive environment in Professor Pavel Jungwirth’s&nbsp;group, my postdoctoral experience with <strong>Professor Dzubiella</strong>, and also the diverse collaborations, thanks to which I&nbsp;understood that the best results often arise from a&nbsp;combination of multiple perspectives that complement each other.</p><h5><strong>What convinced the grant review committee to support your project?</strong></h5><p>The path to support was not entirely straightforward, but we gradually refined the proposal and strengthened it with preliminary results. I&nbsp;believe the decision was driven by the combination of a&nbsp;timely scientific topic, the strong connection between experiments and simulations, and a&nbsp;long-term collaboration that have already yielded concrete, high-quality results.</p><h5><strong>Who else are you collaborating with on the project?</strong></h5><p>On the Czech side, my key collaborator is <strong>Associate Professor Mario Vazdar</strong>, whose expertise covers the interactions of biomolecules with membranes. Members of our groups and doctoral students are also involved in the project.</p><h5><strong>How will you disseminate your project outputs?</strong></h5><p>We will share the results as is standard, in the form of peer-reviewed publications and conference presentations. We plan to make the simulation data available only for selected systems due to their large volume (approx. 10&nbsp;GB per simulation). For other systems, we will provide the inputs, parameters, and analytical procedures that will allow our results to be reproduced or built upon.</p><h5><strong>Will you be communicating the results to the wider public?</strong></h5><p>Yes, definitely. Professional seminars, student theses, and presentations will be a&nbsp;natural part of the project, but we would also be happy to engage in outreach for the wider public.</p><h5><strong>Are you looking for students for this project? And if so, what kind?</strong></h5><p>Yes, we are looking for students. The project offers topics for doctoral students focused on computer modelling, as well as for students with an interest in experiments, thermodynamics, biophysics, or biochemistry. The breadth of the topic, the opportunity to work with modern methods, and the connection to international collaboration are all very attractive features.</p></div>

Jan Heyda: Molecular view of membraneless organelles in collaboration with the USA

<p><strong>The choice between micro-Snyder column concentration and </strong><a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/products?category=362&amp;manufacturerItems=540"><strong>nitrogen blowdown evaporation</strong></a><strong> represents one of the most critical decisions in EPA analytical methodology. Both techniques serve as validated concentration methods across numerous EPA test procedures, yet each offers distinct advantages that make them suitable for different analytical scenarios. Understanding these differences is essential for laboratories seeking to optimize their analytical workflows and ensure regulatory compliance.</strong></p><h3><strong>Understanding the Fundamentals</strong></h3><p>Both concentration techniques serve the same primary purpose: reducing extract volumes to levels suitable for instrumental analysis while maintaining analyte integrity. However, their operational principles differ significantly in terms of temperature requirements, operator involvement, and equipment specifications.</p><p>The micro-Snyder column technique utilizes controlled heat application through a hot water bath maintained at 60-65°C, with the distillation process regulated by the column's three-ball or two-ball design [1, 2]. The technique provides visual indicators of proper operation through actively chattering balls, which signal optimal distillation rates without chamber flooding [2]. In contrast, nitrogen blowdown operates at significantly lower temperatures of 30-35°C, using a gentle stream of filtered nitrogen to facilitate solvent evaporation [3, 4].</p><h3><strong>Widespread EPA Method Applications</strong></h3><h4><strong>Micro-Snyder Column Integration</strong></h4><p>The micro-Snyder column technique demonstrates remarkable ubiquity across EPA analytical methods, appearing as a standard procedure in numerous applications:</p><ul><li><strong>Water Analysis: EPA Method 625</strong> for base/neutral and acid extraction specifies the use of both three-ball macro-Snyder columns for initial concentration (15-20 minutes) and two-ball micro-Snyder columns for final concentration (5-10 minutes) [2]. The method requires pre-wetting columns with 0.5 mL of methylene chloride and maintaining proper distillation rates where "the balls of the column will actively chatter but the chambers will not flood with condensed solvent" [2].</li><li><strong>Organochlorine Analysis: EPA Method 610</strong> for polynuclear aromatic hydrocarbons incorporates micro-Snyder columns for both standard concentration and specialized solvent exchange procedures, including acetonitrile concentration at elevated temperatures of 95-100°C [5].</li><li><strong>Nitrosamine Detection:</strong> <strong>EPA Method 607</strong> utilizes micro-Snyder columns as part of its comprehensive extraction and concentration protocol, with specific volume adjustments to 2.0 mL following concentration [6].</li><li><strong>Advanced Extraction Methods:</strong> <strong>EPA Method 3570</strong> for microscale solvent extraction employs sequential micro-Snyder columns, using both three-ball and two-ball columns in series for optimal concentration control [1].</li></ul><h4><strong>Nitrogen Blowdown Applications</strong></h4><p><a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/article/5392"><strong>Nitrogen blowdown evaporation </strong></a>has gained significant acceptance across EPA methodologies, particularly for applications requiring gentle thermal treatment:</p><ul><li><a target="_blank" rel="noopener noreferrer" href="https://www.organomation.com/what-is-solid-phase-extraction-spe"><strong>Solid Phase Extraction</strong></a><strong>: EPA Method 3535A</strong> explicitly provides nitrogen evaporation as an alternative to micro-Snyder column concentration, recognizing both techniques as equally valid approaches. The method specifies operation in a warm water bath at 30°C with filtered nitrogen that has passed through activated carbon [3].</li><li><strong>Environmental Monitoring: EPA Method 1668</strong> for chlorinated biphenyl congeners incorporates nitrogen blowdown for micro-concentration procedures, utilizing water bath temperatures between 30-60°C . The method emphasizes the importance of controlled evaporation to prevent analyte degradation.</li><li><strong>Pesticide Analysis: EPA Method 1699</strong> for pesticides in environmental matrices specifies nitrogen blowdown procedures with water bath temperatures of 60°C, demonstrating the technique's versatility across different temperature ranges [7].</li><li><strong>PFAS Analysis:</strong> Modern EPA methods for per- and polyfluoroalkyl substances (PFAS), including <a target="_blank" rel="noopener noreferrer" href="https://blog.organomation.com/blog/concentrating-pfas-samples-ahead-of-lcms"><strong>Methods 533 and 537.1</strong></a>, rely heavily on nitrogen blowdown due to the thermal sensitivity of these emerging contaminants [8].</li></ul><h3><strong>Comparative Performance Analysis</strong></h3><h4><strong>Micro-Snyder Column Advantages</strong></h4><ul><li><strong>Standardized Reproducibility:</strong> The micro-Snyder column technique offers inherent standardization through its visual feedback mechanism. The actively chattering balls provide immediate indication of proper operation, reducing operator variability between laboratories [2]. This standardization has contributed to its widespread adoption across EPA methods spanning decades of regulatory use.</li><li><strong>Built-in Safety Features:</strong> The column design incorporates multiple safety elements, including automatic regulation of distillation rates and the 10-minute cooling and draining period that prevents rapid temperature changes [2]. These features minimize the risk of analyte loss due to operator error or equipment malfunction.</li><li><strong>Proven Regulatory Acceptance: </strong>The technique's inclusion in foundational EPA methods like 625, 610, and 607 demonstrates its long-standing regulatory acceptance and proven reliability across diverse analytical applications [2, 5, 6].</li><li><strong>Efficient Heat Transfer: </strong>The controlled temperature environment of 60-65°C provides efficient solvent evaporation while remaining below the degradation threshold for most organic compounds [1, 2].</li></ul><h4><strong>Nitrogen Blowdown Advantages</strong></h4><ul><li><strong>Temperature-Sensitive Analyte Preservation:</strong> Operating at 30-35°C, nitrogen blowdown provides gentler thermal treatment that preserves heat-sensitive compounds [3, 4]. This advantage is particularly crucial for emerging contaminants like PFAS, where thermal degradation can significantly impact analytical results [8].</li><li><strong>Precise Volume Control: </strong>The technique allows operators to achieve exact final volumes through visual monitoring, stopping evaporation at precisely the desired endpoint . This precision is valuable when specific concentration factors are required for regulatory compliance.</li><li><strong>Reduced Equipment Investment:</strong> Nitrogen blowdown requires minimal specialized glassware compared to <a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/products/1904"><strong>Kuderna-Danish</strong></a> apparatus with Snyder columns, making it accessible for laboratories with limited capital budgets [9].</li><li><strong>Enhanced Operator Control: </strong>The real-time monitoring capability allows operators to adjust evaporation rates and respond to unexpected conditions during the concentration process [9].</li></ul><h4><strong>Comparative Limitations</strong></h4><ul><li><strong>Micro-Snyder Column Challenges: </strong>The technique requires significant capital investment in specialized glassware and heating equipment [2]. Additionally, the automated nature of the process provides limited operator control once concentration begins, potentially problematic for samples requiring specific handling.</li><li><strong>Nitrogen Blowdown Limitations: </strong>The technique demands constant operator attention to prevent over-concentration, with organophosphorus pesticides being particularly susceptible to losses from complete dryness. Contamination risks from plastic tubing and the need for precise nitrogen flow control add complexity to routine operations [3].</li></ul><h3><strong>Method Selection Guidelines</strong></h3><h4><strong>Sample Throughput Considerations</strong></h4><p>High-volume environmental laboratories often favor micro-Snyder columns for their automated operation and reduced hands-on time requirements [2]. The technique allows multiple samples to be processed simultaneously with minimal operator intervention, improving laboratory productivity.</p><p>Conversely, laboratories processing smaller sample batches or requiring individual sample optimization may prefer <a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/products/1908"><strong>nitrogen blowdown's flexibility</strong></a> and precise control capabilities [9].</p><h4><strong>Analyte-Specific Requirements</strong></h4><p>Temperature-sensitive compounds, including many pharmaceutical residues and emerging contaminants, benefit from nitrogen blowdown's lower operating temperatures [8, 9]. The 30-35°C operating range significantly reduces thermal stress compared to the 60-65°C requirement for micro-Snyder columns [3].</p><p>For thermally stable environmental pollutants like polynuclear aromatic hydrocarbons and organochlorine compounds, both techniques provide equivalent performance with method selection based on operational preferences [5].</p><h4><strong>Regulatory Compliance Factors</strong></h4><p>Specific EPA methods may designate one technique over another, eliminating choice for particular analytical procedures. However, methods like EPA 3535A that offer both options allow laboratories to select based on their specific capabilities and quality control requirements [3].</p><h4><strong>Contemporary Applications and Future Trends</strong></h4><p>The analytical landscape continues evolving with emerging contaminants and advanced instrumentation. Nitrogen blowdown has gained particular prominence in PFAS analysis due to these compounds' thermal sensitivity and the need for trace-level detection [8]. This trend reflects the technique's adaptability to modern analytical challenges.</p><p>Simultaneously, micro-Snyder columns remain essential for established environmental monitoring programs where long-term data consistency requires standardized procedures [2]. The technique's proven track record supports its continued use in regulatory compliance monitoring.</p><h3><strong>Conclusion</strong></h3><p>Both micro-Snyder column concentration and nitrogen blowdown serve critical roles in EPA analytical methodology, with optimal selection depending on specific analytical requirements, laboratory capabilities, and regulatory constraints. The micro-Snyder column technique excels in standardized, high-throughput applications where proven reliability and regulatory acceptance are paramount. Nitrogen blowdown provides superior performance for temperature-sensitive analytes and applications requiring precise volume control.</p><p>Modern laboratories benefit from understanding both techniques' capabilities, allowing method selection based on analyte properties, sample characteristics, and operational requirements. As analytical chemistry continues advancing with new contaminants and detection challenges, both concentration methods will remain valuable tools in the environmental analyst's toolkit.</p><p>The choice between these techniques ultimately reflects the broader analytical strategy, balancing regulatory compliance, analytical performance, and operational efficiency to achieve reliable environmental monitoring results.</p>

Micro-Snyder Column vs Nitrogen Blowdown: Choosing the Right Concentration Method for EPA Applications

<p><strong>We are pleased to invite you to our upcoming free online webinar on June 11, 2026 focused on one of the most pressing challenges in environmental monitoring and water quality management — PFAS (Per- and Polyfluoroalkyl Substances).</strong></p><p>As regulatory frameworks continue to evolve and compliance deadlines approach, laboratories, water utilities, and environmental professionals need robust, reliable, and cutting-edge analytical solutions to stay ahead.</p><blockquote><p class="cke-user_style-important"><strong>👉</strong><a target="_blank" rel="noopener noreferrer" href="https://events.teams.microsoft.com/event/91d97003-fe33-4dca-b80b-160d9f8a5655@485ca04e-6f74-4050-9764-cdb4bfa89c25"><strong>Registration HERE</strong></a></p></blockquote><p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/ALS_analyzy_PFAS_a9e4a87fbc.jpg" alt="ALS: Advanced PFAS Analytical Services " srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_ALS_analyzy_PFAS_a9e4a87fbc.jpg 245w," sizes="100vw" width="600" height="336"></p><h4><strong>🎤 Our Speaker</strong></h4><p>The webinar will be hosted by <strong>Jana Kováčová, Ph.D., PFAS Regional Lead for Continental Europe Environmental Division</strong>, who has dedicated the last several years to the field of PFAS analysis and determination in ALS laboratories. Jana is a recognized expert in PFAS environmental analytics and will share practical insights and the latest developments in analytical strategies to help your organization achieve and maintain compliance.</p><h4><strong>🎯 What You Will Learn</strong></h4><ul><li>Latest <strong>regulatory developments</strong> and compliance requirements for PFAS in water, including <strong>EU Drinking Water Directive 2020/2184</strong> and its implications for water suppliers and laboratories.</li><li><strong>Regulatory updates for surface water and groundwater</strong> — what's new and what to expect next.</li><li>Overview of <strong>advanced analytical strategies</strong> for PFAS detection and quantification in water matrices and how we analyse PFAS samples.</li><li>Key <strong>analytical challenges</strong> associated with PFAS testing — from ultra-trace detection to matrix interferences and contamination control.</li><li>The critical importance of using tested <strong>sampling containers</strong> and sample preservation to ensure reliable results.</li><li>Illustrative <strong>examples of results</strong> from real-world PFAS water analyses.</li><li>How ALS can support your needs with <strong>accredited PFAS testing services</strong>.</li></ul><h4><strong>👥 Who Should Attend</strong></h4><p>This webinar is designed for our clients, professionals, laboratory and technical staff, scientists, as well as anyone with an interest in analytical chemistry who wants to better understand the occurrence of these "forever chemicals" in the environment. &nbsp;</p><h4><strong>💬 Q&amp;A Session</strong></h4><p>There will be a live Q&amp;A session at the end of the webinar. You are welcome to submit your questions in advance during registration or ask them live on the day.</p><h4><strong>📅 Additional Webinar Info:</strong></h4><ul><li><strong>Platform: </strong>Microsoft Teams (online)</li><li><strong>Time: </strong>10:00 CEST</li><li><strong>Language: </strong>English</li><li><strong>Duration:</strong> approx. 45 - 60 minutes (incl. Q&amp;A)<br>Extras: If you are unable to attend on the day, please register and we will provide you with the recording of the webinar.</li></ul><h4><strong>🔬 About ALS Environmental</strong></h4><p>ALS is a global leader in environmental testing and analytical services, providing accredited PFAS analysis to clients across Europe and beyond. Our dedicated PFAS experts help clients navigate the complex regulatory landscape with confidence.</p><blockquote><p>For further information, please contact us on: <strong>marketing.cz@alsglobal.com</strong></p></blockquote><p>We look forward to welcoming you to this important discussion on PFAS compliance in water.</p>

Invitation to the ALS Webinar PFAS in Water 2026: Achieving Compliance through Advanced Analytical Strategies

Article

Product

Webinars

Academy

Video

Environment

Water

Science and research

For more than 40 years, ALS has provided testing and technical solutions to clients all over the world in a wide range of industries. We have built our global reputation by embracing the latest technologies and innovative methodologies to deliver high quality testing services to clients. ALS is able to leverage a multifaceted international team while remaining agile enough to provide local expertise and personalized solutions to every one of our clients.

ALS Czech Republic

The University of Chemistry and Technology, Prague is a natural centre of first-rate study and research in the area of chemistry in Czechia and is one of the country's largest educational and research institutions focused on technical chemistry, chemical and biochemical technologies, material and chemical engineering, food chemistry, and environmental studies.

UCT Prague

Organomation, founded in 1959, designs and manufactures high-quality nitrogen evaporators and extraction systems. Known for innovation and durability, their lab instruments are used globally for efficient sample preparation with strong customer support.

Organomation

Agilent Technologies

Bruker

Thermo Fisher Scientific

Wiley

Shimadzu Corporation

Waters Corporation

<p><strong>LC-MS/MS is rapidly becoming the gold standard for quantifying different classes of analytes in endocrinology research.  The power of greater selectivity and analytical sensitivity using LC-MS/MS is critical in understanding the status of endocrine biochemical pathways.  The enhanced performance observed on these platforms provides increased confidence in the results, enabling you to make better decisions based on more accurate information.</strong></p>
<p>Greater analytical sensitivity is a goal that drives improvements in precision, leading to clearer insights into results down to low physiological concentrations.  Here we will discuss the latest introduction to the Waters MassTrak™ IVD system family, which is shown to be analytically sensitive and efficient, helping to reduce cost and improve the quality of your data. </p>
<p>Learning objectives: </p>
<ul>
<li><p><strong>An introduction to the latest addition to Waters MassTrak IVD System for clinical laboratories</strong></p>
</li>
<li><p><strong>The importance of selectivity in endocrinology research in obtaining high quality data</strong></p>
</li>
<li><p><strong>How the latest addition to Waters MassTrak IVD System addresses the needs of those key endocrinology research applications, including steroid hormone analysis</strong></p>
</li>
</ul>
<blockquote>
<p><strong>Presenter:</strong> Dominic Foley (Principal Scientist, Waters Corporation)</p>
</blockquote>
<blockquote>
<p>Dominic is a Principal Scientist working at Waters Mass Spectrometry Headquarters in Wilmslow, UK. Having joined the company in September 2013, he has specialized in the development of LC-MS/MS clinical research applications, with expertise in steroid hormone analysis and protein/peptide quantification. In his role, he also collaborates with clinical customers in the development and implementation of LC-MS/MS methods in their laboratories.</p>
</blockquote>
<blockquote>
<p>Dominic has worked in separation sciences for 14 years, following his ambition of improving the quality of healthcare. He started his career with ICON Development Solutions, a CRO in the north of the UK, where he worked as a LC-MS/MS method development and validation scientist supporting DMPK studies in drug discovery. In 2012, he joined Thermo Fisher Scientific to work in their Chromatography R&amp;D team as a Technical Support Specialist, working on the development of new chromatography and sample preparation products.</p>
</blockquote>
<blockquote>
<p>Dominic received his BSc (Hons) in Biochemistry from the University of Manchester in 2006. He has presented his work at conferences around the world and has several publications in both the Microchemical Journal and the Journal of Chromatography A.</p>
</blockquote>
<blockquote>
<p><strong>Presenter:</strong> David Ballantyne (Principal Product Manager, Waters Corporation)</p>
</blockquote>
<blockquote>
<p>David Ballantyne is a Principal Product Manager at Waters Corporation, working within the Global Clinical Diagnostics Portfolio Management team. Having joined the company in 2005, he has held multiple roles throughout Manufacturing and R&amp;D. David has a background in Electrical and Mechanical Engineering and began his career at Waters supporting GC-MS/MS technologies including Tandem Quadrupole and Magnetic Sector Mass Spectrometry.</p>
</blockquote>
<blockquote>
<p>In 2018 he moved to his role in Product Management where is focus changed to Clinical Diagnostics, with a particular focus on LC – MS/MS Instrumentation and Informatics solutions. Over the last 5 years David has spent much of his time focused on understanding customer problems and translating them into new solutions.</p>
</blockquote>


Waters Corporation: The Evolving Power of LC-MS/MS Technology within Endocrinology

The Evolving Power of LC-MS/MS Technology within Endocrinology

Here we will discuss the latest introduction to the Waters MassTrak™ IVD system family for clinical laboratories.

The Evolving Power of LC-MS/MS within Endocrinology

<p><strong>While the application of Mass Spectrometry (MS) Imaging is rapidly growing, its usage is largely limited to experienced scientists. Shimadzu’s Benchtop MALDI-TOF, however, offers a compact, affordable, and user-friendly option to all. Moreover, when combined with the automated matrix applicator (iMLayer suite), our Benchtop MALDI-TOF provides a game-changing solution suitable to all users regardless of skill level.</strong></p>
<p>In this webinar, we will showcase how our workflow offers simplified sample preparation, a complete imaging solution in a compact footprint, an imaging starter kit customizable based on your needs, and intuitive software for data analysis. This workflow will be suitable in research applications from analysis of small molecules such as lipids to large molecules such as protein, peptides, polymers etc.</p>
<p>Join us to learn how you can become an expert in MS imaging with Shimadzu&#39;s MALDI-TOF today.</p>
<p>Learning Objectives:</p>
<ul>
<li><strong>Learn how Shimadzu offers total solutions for MALDI Imaging</strong></li>
<li><strong>Learn about our patented Two-step Vapour Deposition Method for optimal sample preparation</strong></li>
<li><strong>Learn about our user-friendly interface for easy data analysis of MALDI Images</strong></li>
<li><strong>Applications of Shimadzu&#39;s Benchtop MALDI Imaging suite</strong></li>
</ul>
<blockquote>
<p><strong>Presenter:</strong> Naatasha Isahak (Product Specialist, Shimadzu (Asia Pacific) Pte Ltd)</p>
</blockquote>
<blockquote>
<p>Naatasha Isahak is a Product Specialist for MALDI and Life Sciences Products from Shimadzu Asia Pacific Pte Ltd. She has received her PhD from the University of Sydney (Chemistry) working on surface initiated polymerisation on silica nanoparticles using RAFT polymerisation and bioorthogonal conjugation of peptides using Native Chemical Ligation. She then spent 5 years working on developing platforms for stem cells and organoids characterization that included working with microfluidic devices and helical polymers. Naatasha joined Shimadzu in 2022 to expand her experiences to MALDI characterization on materials and biological samples.</p>
</blockquote>


Shimadzu: MALDI-Imaging For All: A Researcher’s Guide

MALDI-Imaging For All: A Researcher’s Guide

Join us to learn how you can become an expert in MS imaging with Shimadzu's MALDI-TOF today.

<ul>
<li><p>Wait what?! Who knew!? There are so many things that a mass spec can do.</p>
</li>
<li><p>I&#39;ve used it for years, yes this may be true.</p>
</li>
<li><p>I&#39;ve processed some samples, more than a few.</p>
</li>
<li><p>But between me and you, I had no idea all the things it could do!</p>
</li>
<li><p>From sample prep to separation, you just won&#39;t believe…</p>
</li>
<li><p>All of the tips and tricks we have up our sleeve.</p>
</li>
<li><p>So, take a few minutes, about 15 should do.</p>
</li>
<li><p>And learn all the things your mass spec can do.</p>
</li>
</ul>
<p><strong>Electrospray ionization (ESI) is the most common ionization technique used in LC-MS, however not all samples are best analyzed by ESI.  Atmospheric Pressure Chemical Ionization (APCI) is a complementary technique that can work well with small molecules that are more non-polar or neutral. Considerations for solvent and mobile phase additives to optimize APCI performance will be discussed.</strong></p>
<blockquote>
<p><strong>Presenter:</strong> Emily Parry, PhD (LC/MS Applications Scientist, Agilent Technologies, Inc.)</p>
</blockquote>
<blockquote>
<p>Emily has been with Agilent for four years. Prior to joining Agilent, Emily developed methods for environmental contaminants in a variety of human and environmental matrices using both targeted and untargeted mass spectrometry techniques. She worked as a researcher at the Environmental Protection Agency (EPA) and Public Health Institute. She received her Ph.D. degree in Environmental Chemistry from the University of California, Davis.</p>
</blockquote>


Agilent Technologies: From Liquid to Ions…. Eliminate your Fears switching from Electrospray ionization (ESI) to Atmospheric Pressure chemical Ionization (APCI)

From Liquid to Ions…. Eliminate your Fears switching from Electrospray ionization (ESI) to Atmospheric Pressure chemical Ionization (APCI)

ESI vs. APCI. Considerations for solvent and mobile phase additives to optimize APCI performance will be discussed.

From Liquid to Ions…. Switching from ESI to APCI

<p>Dear user and other PaSER interested customers,</p>
<p>You are hereby invited to our 2nd Virtual PaSER Workshop. A lot of new possibilities has been introduced since last time – including, but not limited to PaSER Novor for de novo sequencing of dda-PASEF® data on the PaSER Box as well as TIMS DIA-NN 2.0 -which will be demonstrated during this Workshop. Data virtualization has been a requested feature – and this is now possible with Mass Dynamics for PaSER. Not limited to above – stay tuned for even more approaching features, we will discuss as well.</p>
<h3><strong>The tentative agenda looks like this:</strong></h3>
<h5><strong>1:00 – 1:15 pm:  Introduction</strong></h5>
<ul>
<li>Willy Bjørklund</li>
</ul>
<h5><strong>1:15 – 1: 35pm:  New Applications on the timsTOF Platform</strong></h5>
<ul>
<li>Lars Kristensen (Field Application Specialist)</li>
</ul>
<h5><strong>1:35 – 1:55 pm:  PaSER as a bioinformatic platform - what’s new and what’s coming</strong></h5>
<ul>
<li>Jonathan Krieger (Software R&amp;D Department)</li>
</ul>
<h5><strong>5 minute break</strong></h5>
<h5><strong>2:00 – 2:20 pm: Live Demo/workshop of PaSER</strong></h5>
<ul>
<li>Tharan Srikumar (Software R&amp;D Department)</li>
</ul>
<h5><strong>2:20 – 2:50 pm: Mass Dynamics</strong></h5>
<ul>
<li>Mark Condina and Giuseppe Infusini</li>
</ul>
<h5><strong>2:50 – 3:10 pm: Questions and discussions</strong></h5>
<h5><strong>3:10 – 3:15 pm:  Conclusion</strong></h5>
<ul>
<li>Willy Bjørklund</li>
</ul>
<p>We aim for a lively interaction so take the timing as an indication. Please feel free to share with colleagues or others you think could benefit from attending this workshop. Looking forward to “meet”</p>


Bruker Virtual PaSER Workshop

Dear user and other PaSER interested customers, You are hereby invited to our 2nd Virtual PaSER Workshop. 

<p><strong>This webinar will focus on untargeted LC/MS Omics solutions that will provide the biological insights needed to produce meaningful results. An emphasis will be spent on an End-to-End HILIC metabolomics workflow for our LC/Q-TOF platform.</strong></p>
<p>This includes automate sample preparation for cells and plasma, a Bio LC that is fit for purpose for metal sensitive analysis, robust and transferable HILIC chromatography, the 6546 LC/Q-TOF data independent analysis of samples, with an ID workflow that includes a new HILIC PCDL with 500 core metabolism analytes with spectra and retention time annotation.</p>
<p>For unknowns not found in Agilent PCDLs, SIRIUS/CSI:FingerID which uses AI predict structure from spectra and conducts online identification search will be demonstrated. A complementary targeted multi-omics workflow will be briefly mentioned before sharing the new Ion Mobility and ExD technologies for high end LC/MS Omics investigations.</p>
<blockquote>
<p><strong>Presenter:</strong> Karen E. Yannell (Omics Workflow Specialist, Agilent Technologies)</p>
</blockquote>
<blockquote>
<p>Karen E. Yannell is an Omics Workflow Specialist at Agilent Technologies. She is an expert in small molecule high throughput analysis by triple quadrupole (TQ) and quadrupole time-of-flight (Q-TOF) mass spectrometry for applied markets. Her recent work has focused on developing targeted metabolomics methods and routine Q-TOF workflows for both expert and non-expert users alike. Previously, Karen worked on forensic, metabolomics, and biomarker discovery applications with ambient ionization sources. She received her PhD in Analytical Chemistry from Purdue University where studied under the advisement of Prof. R. Graham Cooks. </p>
</blockquote>
<blockquote>
<p><strong>Presenter:</strong> Dr. Martin Graf-Utzmann (Editor, Wiley Analytical Science, Moderator)</p>
</blockquote>
<blockquote>
<p>Dr. Martin Graf-Utzmann has a Ph.D. in Theoretical Chemistry and is an editor for Wiley Analytical Science. His interests are mainly Laboratory Automation, Digitalization, and Lab Equipment.</p>
</blockquote>


Wiley Analytical Science: Jump Start Your LC/Q-TOF Omics Investigation with Reliable Workflows

Jump Start Your LC/Q-TOF Omics Investigation with Reliable Workflows

This webinar will focus on untargeted LC/MS Omics solutions that will provide the biological insights needed to produce meaningful results.

Your LC/Q-TOF Omics Investigation with Reliable Workflows

<p><strong>This year we invite you to ignite your mind to Be Curious about what Ion chromatography (IC) can do with its versatility in many detections across the IC application spectrum to improve your workflows and solve challenges.</strong></p>
<p>During this three day virtual event, learn from a panel of experts how the latest IC applications are helping colleagues achieve breakthroughs, and walk away with valuable information on how advancements in IC can increase laboratory analytical capabilities. </p>
<p>Although each day is convenient for a specific region, you can attend any session on any day. All sessions and workshops will be available for on-demand viewing after the event concludes.</p>
<h3><strong>Day 1 Agenda | April 18 | North and South America</strong></h3>
<p>Discover IC column development, and where it’s headed with mass spectrometry, as they can be an integral detection for carbohydrate profiling and environmental metabolites characterization. Learn how standalone IC can solve industrial samples and degradation products with comprehensive IC information, all at once.</p>
<h5><strong>11:30 EDT: Opening Plenary: The Past, Present, and Future of IC Column Development</strong></h5>
<ul>
<li>Alexandra Zatirakha (Thermo Fisher Scientific, IC/SP R&amp;D, Sunnyvale)</li>
</ul>
<h5><strong>12:30 EDT: Characterizing Carbohydrate Degradation Products from Bacteroides Thetaiotaomicron to Understand Bacterial Dextran Utilization in the Gut</strong></h5>
<ul>
<li>Neil Rumachik (Thermo Fisher Scientific, IC/SP R&amp;D, Sunnyvale)</li>
<li>Fiona Cuskin (Newcastle University, UK)</li>
</ul>
<h5><strong>1:30 PM EDT: Toward Comprehensive Chemical Characterization of Metabolomic Using Orbitrap Fusion Tribrid Mass Spectrometer Coupled with Ion and Liquid Chromatography Techniques: Dissolved Organic Matter as an Example</strong></h5>
<ul>
<li>Hussain Abdulla (Department of Physical and Environmental Sciences, Texas A&amp;M University-Corpus Christi)</li>
</ul>
<h5><strong>2:30 PM EDT: The Use of Ion Chromatography in the Monitoring of Degradation Products from the Electrochemical Treatment Of Organic Compounds</strong></h5>
<ul>
<li>Emily Tossi (Federal University of Rio Grande do Norte)</li>
</ul>
<h5><strong>3:30 PM EDT: Ion Chromatography as a Tool for Industrial Problem Solving</strong></h5>
<ul>
<li>Isaac Negrete and Stephen Fosdick (Dow)</li>
</ul>
<h5><strong>4:30 PM EDT: Workshop: Everything, Everywhere, All at Once IC!</strong></h5>
<ul>
<li>Kelly Femrite (IC/SP Product Support, Sunnyvale)</li>
<li>Carl Fisher (IC/SP Product Marketing, Sunnyvale)</li>
<li>Criss Corchard-Keeler (Service Marketing Manager, CMD/MOL Thermo Fisher Scientific)</li>
</ul>


Thermo Fisher Scientific: IC Symposium 2023

IC Symposium 2023 - Day 1

Join us for the 2023 Global IC Symposium! North and South America

<p><strong>This year we invite you to ignite your mind to Be Curious about what Ion chromatography (IC) can do with its versatility in many detections across the IC application spectrum to improve your workflows and solve challenges.</strong></p>
<p>During this three day virtual event, learn from a panel of experts how the latest IC applications are helping colleagues achieve breakthroughs, and walk away with valuable information on how advancements in IC can increase laboratory analytical capabilities. </p>
<p>Although each day is convenient for a specific region, you can attend any session on any day. All sessions and workshops will be available for on-demand viewing after the event concludes.</p>
<h3><strong>Day 2 Agenda | April 19 | Europe and Africa</strong></h3>
<p>Untap the versatility of ion chromatography with challenging analytes such as chlorate, sulfite, cationic polar pesticides, and glycoprotein sialic acid in tricky matrices while optimizing your workflow.</p>
<h5><strong>9:00 AM CET: Opening Plenary: Untapped Potential in Ion Chromatography for Resolving Analytical Challenges</strong></h5>
<ul>
<li>Detlef Jensen (Thermo Fisher Scientific, IC Expert)</li>
</ul>
<h5><strong>11:00 AM CET: Determination of Chlorate in Agar Samples Using Ion Chromatography</strong></h5>
<ul>
<li>Flavio Zanetti (Biopolife Srl, Trieste, Italy)</li>
</ul>
<h5><strong>12:00 PM CET: Determination of Sulphur Dioxide in Foods by Ion Chromatography</strong></h5>
<ul>
<li>Noel Finn (Public Analyst Laboratory, St. Finbarr’s Hospital, Douglas Road, Cork)</li>
</ul>
<h5><strong>1:00 PM CET: 30 min Lunch</strong></h5>
<h5><strong>1:30 PM CET: Analysis of Polar Cationic Pesticides by IC-MS</strong></h5>
<ul>
<li>Anatte Margalit (DAFM)</li>
</ul>
<h5><strong>2:30 PM CET: Determination of Glycoprotein Sialic Acid Composition Using HPAE-PAD in Dual Eluent Generation Cartridge Mode</strong></h5>
<ul>
<li>Jingli Hu (Thermo Fisher Scientific, IC/SP Applications, Sunnyvale)</li>
</ul>
<h5><strong>3:30 PM CET: Optimizing Your IC Workflow Using Chromeleon CDS</strong></h5>
<ul>
<li>Dan Talbot (Thermo Fisher Scientific, IC/SP Senior, Application Sales Support, UK &amp; Ireland)</li>
</ul>


IC Symposium 2023 - Day 2

Join us for the 2023 Global IC Symposium! Europe and Africa

<p><strong>This year we invite you to ignite your mind to Be Curious about what Ion chromatography (IC) can do with its versatility in many detections across the IC application spectrum to improve your workflows and solve challenges.</strong></p>
<p>During this three day virtual event, learn from a panel of experts how the latest IC applications are helping colleagues achieve breakthroughs, and walk away with valuable information on how advancements in IC can increase laboratory analytical capabilities. </p>
<p>Although each day is convenient for a specific region, you can attend any session on any day. All sessions and workshops will be available for on-demand viewing after the event concludes.</p>
<h3><strong>Day 3 Agenda | April 20 | Asia Pacific</strong></h3>
<p>Expand the world of electrochemistry applications and IC hyphenation with high-resolution mass spectrometry and understand how Inductively Coupled Plasma Spectrometry can speciate isotopes while simplifying Pharmacopeia QC analysis and keeping your IC in top-notch condition.</p>
<h5><strong>11:00 AM SGT: Opening Plenary: Electrochemical Detection and Its Application in Ion Chromatography</strong></h5>
<ul>
<li>Yan Liu (Thermo Fisher Scientific, IC/SP R&amp;D, Sunnyvale)</li>
</ul>
<h5><strong>12:00 PM SGT: Application of Anion Chromatography Coupled High-Resolution Mass Spectrometry to Increase Cellular Metabolite Coverage</strong></h5>
<ul>
<li>Vinzenz Hofferek (McConville Lab, Department of Biochemistry and Pharmacology)</li>
</ul>
<h5><strong>1:00 PM SGT: Analysis of Anhydrosugars and Xylooligosaccharides by Ion Chromatography with Electrospray Lithium Cationisation-Triple Quadrupole Tandem Mass Spectrometry</strong></h5>
<ul>
<li>Dr. Estrella Sanz Rodriguez (Natural Products Analysis, Australian Centre for Research on Separation Science (ACROSS), University of Tasmania)</li>
</ul>
<h5><strong>2:00 PM SGT: You Gotta Keep ‘Em Separated: Novel IC Applications for Subsequent Isotopic Analyses by Rapid and/or Hyphenated Techniques</strong></h5>
<ul>
<li>Dr. Brandon Mahan (College of Science and Engineering, James Cook University)</li>
<li>Grace Manestar (IsoTropics PhD Candidate)</li>
</ul>
<h5><strong>3:00 PM SGT: Use of Ion Chromatography in Pharmaceutical Quality Control</strong></h5>
<ul>
<li>Catherine Frankis and Stella Planou (Reading Scientific Services Ltd., Reading Science Centre, Whiteknights Campus)</li>
</ul>
<h5><strong>4:00 PM SGT: Tips on Keeping Your Ion Chromatography in Top-Notch Condition</strong></h5>
<ul>
<li>Ryan Ong (Thermo Fisher Scientific, IC/SP Application Sales Support, Singapore)</li>
</ul>


IC Symposium 2023 - Day 3

Join us for the 2023 Global IC Symposium! Day 3 | Asia Pacific.

<p><strong>Get ready for Nitrosamines - The LC/MS Edge, a series of virtual connect that explores the latest updates, insights, and technical knowledge on nitrosamines in India.</strong></p>
<p>Join us for the first session, focused on the growing concern of nitrosamines in the Indian pharmaceutical industry. Learn about the perspective of Indian Pharmacopoeia on regulation, evolving market landscape, growth opportunities and the role of LC-MS/MS in nitrosamine assessment studies. Experts will discuss the perspectives of evolving regulations and how companies can adapt these solutions, followed by a Q&amp;A discussion. Nitrosamines pose a significant risk to public health, making it crucial for companies to be aware of the latest regulations and market trends. Stay ahead of the curve and ensure compliance with latest regulatory requirements. Don&#39;t miss out on this valuable opportunity. </p>
<p>Why should you attend?</p>
<ul>
<li><strong>Gain insights into the perspective of Indian Pharmacopoeia on assessment of nitrosamines.</strong></li>
<li><strong>Understand the current market landscape and growth opportunities.</strong></li>
<li><strong>Learn about compliance requirements and how to navigate them.</strong></li>
<li><strong>Stay up-to-date on the latest trends and updates related to nitrosamines in India.</strong></li>
<li><strong>Improve your professional development &amp; scientific understanding by enhancing your knowledge and skills related to nitrosamines assessment workflows and LC/MS.</strong></li>
</ul>
<blockquote>
<p><strong>Presenter:</strong> Mr. Arvind Kumar Sharma (Scientific Assistant, Indian Pharmacopoeia Commission, Ministry of Health &amp; Family Welfare - Government of India)</p>
</blockquote>
<blockquote>
<p>With six years of experience as a Scientific Assistant at Indian Pharmacopoeia Commission, he has played a key role in the current development of Indian Pharmacopoeia Reference Substances (IPRS) and Impurity Reference Substances. He has been engaged in the preparation and updating of draft monographs for publishing in Indian Pharmacopoeia (IP). Additionally, he has played a major role in the development of the latest edition of the National Formulary of India 2021 and has been involved in work related to the Pharmacovigilance Programme of India (PvPI). He holds a a M. Pharmacy in Pharmacology from Sinhgad Institute of Pharmaceutical Sciences, Pune and a B. Pharmacy from the College of Pharmacy, IPS Academy Indore. He has authored several articles published in international journals and organized and represented IPC at various national and international conferences and workshops. He has also participated in joint inspections for registration of manufacturing units and testing laboratories.</p>
</blockquote>
<blockquote>
<p><strong>Presenter:</strong> Dr Kuldeep Sharma (Sales Development Manager - Pharma, Agilent Technologies India Pvt Ltd)</p>
</blockquote>
<blockquote>
<p>Kuldeep Sharma has over 19 years of experience in area/s of Bioanalytical research, Drug metabolism &amp; pharmacokinetics and Pharma regulatory compliance. He has accomplished PhD in Biotechnology. His professional journey covers over 12 years in Analytical research (associated with R&amp;D’s of Zydus Cadila, Lambda, Pliva and Jubilant Biosys) and last 7 years in analytical instruments sales, marketing &amp; business development. With over 21 research articles published in international Journals, He presents convention of continues learning.</p>
</blockquote>


Agilent Technologies: Nitrosamines - The LC/MS Edge 1st Edition: Indian Pharmaceutical Industry Perspective & Evolving Regulatory Landscape

Nitrosamines - The LC/MS Edge 1st Edition: Indian Pharmaceutical Industry Perspective & Evolving Regulatory Landscape

Join us for the first session, focused on the growing concern of nitrosamines in the Indian pharmaceutical industry.

Nitrosamines - The LC/MS Edge 1st Edition

<ul>
<li><p>Wait what?! Who knew!? There are so many things that a mass spec can do.</p>
</li>
<li><p>I&#39;ve used it for years, yes this may be true.</p>
</li>
<li><p>I&#39;ve processed some samples, more than a few.</p>
</li>
<li><p>But between me and you, I had no idea all the things it could do!</p>
</li>
<li><p>From sample prep to separation, you just won&#39;t believe…</p>
</li>
<li><p>All of the tips and tricks we have up our sleeve.</p>
</li>
<li><p>So, take a few minutes, about 15 should do.</p>
</li>
<li><p>And learn all the things your mass spec can do.</p>
</li>
</ul>
<p><strong>An easy to follow guide detailing how to set MS scan parameters for an LCMS experiment will be presented.  Scan speeds for reproducible quantitation, chromatographic resolution, retention time definition, proper threshold adjustment for optimum datafile size, and how this can result in faster processing times will all be discussed.</strong></p>
<blockquote>
<p><strong>Presenter:</strong> Rebecca Glaskin, Ph.D. (LC/MS Application Scientist, Agilent Technologies, Inc.)</p>
</blockquote>
<blockquote>
<p>Rebecca Glaskin is an LC/MS Application Scientist at Agilent with a focus on BioPharma applications supporting the LC-Q/TOF and IM-QTOF platforms. Prior to joining Agilent, Rebecca received her Ph.D. in analytical chemistry from Indiana University in the lab of Professor David Clemmer. While there she designed and constructed home-built instruments, pushing the limits of the mobility resolution that can be obtained with a circular drift tube for the separation of biomolecules (peptides, proteins, carbohydrates, and metabolites). While there, she also studied hydrogen/deuterium exchange of proteins in the gas-phase as a function of time and pressure. Rebecca then went to Boston University as a Postdoctoral Associate in the lab of Professor Catherine Costello to develop a database containing collision cross section values for glycans, peptides, and glycopeptides utilizing Agilent Technologies 6560 IM-QTOF. This database can be used to determine how the collision cross section is altered with the addition of individual saccharide units. The trendlines obtained from this database will be used to predict collision cross sections for glycopeptides based on the conformation and structure of the specific glycoform.</p>
</blockquote>
<blockquote>
<p><strong>Presenter:</strong> Jim Lau, PhD (HRAMS LC/MS Application Engineer, Agilent Technologies, Inc.)</p>
</blockquote>
<blockquote>
<p>Jim Lau received his Ph.D. From the University of Colorado. There he worked in the laboratories of Peter Albersheim and Robert Shapiro. This work involved the structure elucidation of plant natural products and, in particular, elucidating the structures of oligosaccharides derived from plant cell wall polysaccharides. This work was done in the early days of LCMS and made use of DLI-LCMS and (at the time) recently invented Thermospray-LCMS.</p>
</blockquote>
<blockquote>
<p>After the completion of his Ph.D., Jim joined Hewlett-Packard to work on LCMS ionization techniques with Paul Goodley during the early days of Electrospray-LCMS. He then moved to work on field applications and collaborations with Hewlett-Packard’s LCMS customers. More than 30 years later, Jim continues to work with Agilent’s customers in High Resolution Accurate Mass applications of LCMS. While involved in many areas of HRAMS LCMS, his recent work has focused on the area of Screening/Qual&amp;Quant of small molecules and on the high throughput confirmation of oligonucleotide synthesis.</p>
</blockquote>


Agilent Technologies: How to set MS Scan Parameters for your LCMS Experiment

How to set MS Scan Parameters for your LCMS Experiment

An easy to follow guide detailing how to set MS scan parameters for an LCMS experiment will be presented.

LCMS webinars focusing on LC/MS - page 93