LCMS webinars focusing on LC/MS - page 40

Pushing the leading edge in next generation quantitative proteomics

Pushing the leading edge in next generation quantitative proteomics

This presentation will provide a technical overview of the new reagents in the context of experimental design, sample preparation, LC-MS analysis and data processing.
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Already taken place We, 1.1.2025
Thermo Fisher Scientific
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Pushing the leading edge in next generation quantitative proteomics
BOOST channel Tandem Mass Tag (TMT) approach: quantitation of more than 5,000 unique pTyr sites

BOOST channel Tandem Mass Tag (TMT) approach: quantitation of more than 5,000 unique pTyr sites

In this webinar you will learn about using of pervanadate treated cells as BOOST channel for phosphotyrosine data acquisition.
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Already taken place We, 1.1.2025
Thermo Fisher Scientific
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BOOST channel Tandem Mass Tag (TMT) approach: quantitation of more than 5,000 unique pTyr sites
Mastering QC Oligonucleotide LC/MS in GMP Labs

Mastering QC Oligonucleotide LC/MS in GMP Labs

This webinar introduces the Oligo Analysis Accelerator for OpenLab CDS, a software that streamlines analytical workflows with a user-friendly interface.
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Already taken place We, 1.1.2025
Technology Networks
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Mastering QC Oligonucleotide LC/MS in GMP Labs
Panel discussion on improving dairy safety and quality frameworks

Panel discussion on improving dairy safety and quality frameworks

The panel will discuss advanced technologies for testing adulteration, pesticides, and heavy metals, and share tips on improving workflows and aligning with regulations.
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Already taken place We, 1.1.2025
Agilent Technologies
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Panel discussion on improving dairy safety and quality frameworks
Ensuring Beauty is Safe: Shimadzu's Solutions for Cosmetic Product Testing

Ensuring Beauty is Safe: Shimadzu's Solutions for Cosmetic Product Testing

This webinar highlights key analytical challenges in cosmetics testing, covering fragrance analysis, UV filters in sunscreens, and heavy metals, with a focus on sensitivity and reproducibility.
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Already taken place Tu, 31.12.2024
Shimadzu Corporation
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Ensuring Beauty is Safe: Shimadzu's Solutions for Cosmetic Product Testing
Pushing the Boundaries of MS-Based Clinical Proteomics: Taking Biology Beyond ID Numbers

Pushing the Boundaries of MS-Based Clinical Proteomics: Taking Biology Beyond ID Numbers

This session shows how ZT Scan DIA is transforming clinical proteomics, enabling scalable, high-specificity workflows that bridge biomarker discovery and clinical implementation.
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Already taken place Tu, 31.12.2024
Wiley
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Pushing the Boundaries of MS-Based Clinical Proteomics: Taking Biology Beyond ID Numbers
Overcoming LC Analytical Challenges in Small Molecule Kinase Inhibitor Development

Overcoming LC Analytical Challenges in Small Molecule Kinase Inhibitor Development

This webinar addresses analytical challenges in kinase inhibitor development, including purification from biological fluids, improved analyte recovery, and conditions enabling HRMS detection.
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Already taken place Tu, 31.12.2024
Waters Corporation
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Overcoming LC Analytical Challenges in Small Molecule Kinase Inhibitor Development
Characterizing PROTACs: Scientific Approaches to Overcome LC Analytical Barriers

Characterizing PROTACs: Scientific Approaches to Overcome LC Analytical Barriers

This session discusses analytical challenges in PROTAC drug discovery, including degradation assessment and managing non-specific adsorption during compound development.
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Already taken place Tu, 31.12.2024
Waters Corporation
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Characterizing PROTACs: Scientific Approaches to Overcome LC Analytical Barriers
Biopharma ll: MAM Intro

Biopharma ll: MAM Intro

BioPharma II: MAM Introduction – presented by Melissa Sato, BioPharma Software Workflow Manager at Agilent.
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Already taken place Tu, 31.12.2024
Agilent Technologies
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Biopharma ll: MAM Intro
Biopharma ll: Multi-Attribute Method (MAM): Transforming Biopharmaceutical Characterization

Biopharma ll: Multi-Attribute Method (MAM): Transforming Biopharmaceutical Characterization

This talk introduces the Multi-Attribute Method (MAM) as a modern LC-MS workflow for biopharmaceutical characterization, focusing on QC implementation, regulatory aspects, and software-driven best practices.
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Already taken place Tu, 31.12.2024
Agilent Technologies
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Biopharma ll: Multi-Attribute Method (MAM): Transforming Biopharmaceutical Characterization
 

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