Utilizing a 3D Spheroid Model and Live-Cell Analysis for Compound Profiling

Case Studies Using the iQue® HTS Platform

A Leap in Small Molecule Sensitivity

Gentle automated organoid transfer and live-cell analysis to improve reproducibility across complex 3D models.

Learn how pH-sensitive probe–based assays and multiplexed cytometry analysis can be applied to quantitatively evaluate antibody internalization across multiple cell types in a high-throughput workflow.

Access our comprehensive application note, "Best Cleaning Practices for Cubis® II Balances," to unlock expert insights and recommendations for preserving the cleanliness and precision of your Sartorius laboratory balance.

Are you tired of struggling with imperfect laboratory conditions that affect the accuracy and precision of your analytical instruments? Look no further than the Cubis® II Ultra-High Resolution Balances from Sartorius.

Uncover the secret to achieving unparalleled precision in your lab with the Cubis II Ultra-High Resolution Balances and its revolutionary Advantage Ionizer. Access our exclusive application note to unlock the strategies for mastering weighing in charged environments and transform your lab experience

Learn how single-cell dissociation and multiparametric marker analysis can be applied to objectively assess brain organoid differentiation in a high-throughput workflow.

3D organoids and advanced cell models are powerful—but difficult to handle, monitor, and quantify. The CellCelector Flex enables automated organoid transfer, non-invasive live-cell imaging, and objective morphological analysis

Assessing the activity profile of a compound is crucial in any drug discovery strategy, especially when profiling large numbers of compounds (ranging from 100 to 100,000) in early-stage programs.

Accurate assessment of mesenchymal stem cell (MSC) identity and differentiation is essential in both research and clinical applications—especially in the fast-moving field of regenerative medicine.

Demonstrating biosimilarity throughout upstream and downstream production processes is crucial. However, screening all potential candidates using standard analytical methods can be challenging.

As the biosimilar market continues to expand, the need for efficient, cost-effective, and reliable development processes becomes paramount.

A major mechanism of action for therapeutic monoclonal antibodies is the initiation of effector function via binding to Fc gamma receptors (FcγRs) expressed on the surface of immune effector cells.

Are you striving to maintain the highest quality standards in mesenchymal stem cell (MSC) research or clinical applications?

Mesenchymal stem cells (MSCs) are revolutionizing regenerative medicine with their ability to differentiate into critical cell types like osteoblasts and adipocytes.

Are you struggling with the transfection of hard-to-modify lymphocytes such as T cells, B cells, and NK cells? Sartorius' jetMESSENGER® mRNA transfection reagent offers a high-efficiency, non-viral solution to deliver mRNA into these challenging cells

Matching the ever-demanding regulatory needs of the pharmaceutical industry can be challenging

The development of immunetherapeutics has seen a marked increase in recent years

Current status from USP, Ph.Eur., JP, ChP

In this in-depth white paper from Sartorius, you will discover how live-cell monitoring and real-time imaging can optimize advanced cell culture workflows—without disturbing your samples.

Optimize Lab Efficiency, Accuracy, and Compliance for Electronic Pipettes and Lab Balances

This white paper summarizes what has changed with the latest revisions in the major global standards,United States Pharmacopeia (USP), European Pharmacopoeia (Ph.Eur.), Japanese Pharmacopoeia (JP), and Chinese Pharmacopoeia (ChP).

Developing biosimilars requires rigorous analytical characterization to ensure safety, efficacy, and regulatory approval.

Every laboratory measurement carries some level of uncertainty—but in regulated environments, uncontrolled variation can compromise compliance, data integrity, and research outcomes.

Drug development and production is challenging. Avitide, based in Lebanon, New Hampshire, provides on-demand development and supply of high-performance affinity purification resins for the manufacture of biotherapeutic drug molecules.

Maintaining accuracy and compliance in liquid handling is critical for laboratory success. This white paper, Gravimetric Calibration and Testing of POVA According to ISO 8655:2022, provides a comprehensive guide to help you

This white paper offers a comprehensive guide on optimizing the performance of analytical balances by addressing variables that impact accuracy, stability, and speed.

This comprehensive guide introduces cutting-edge technologies that are transforming the field!

In the rapidly advancing world of biomedical science, the demand for more accurate, physiologically relevant models has never been greater.

Sterility testing is critical to ensuring that sterile products, such as pharmaceuticals and medical devices, are free of contaminating viable microorganisms. This critical test assesses whether a manufactured batch of a sterile product is ready for release.

Mesenchymal stem cells (MSCs) are a type of adult stem cell with the unique ability to develop into diverse cell types, including bone, cartilage, muscle, and fat.

Staying compliant with FDA 21 CFR Part 11 regulations is critical in pharmaceutical and life science laboratories.

In pharmaceutical quality control, even the smallest deviation can put safety, compliance, and product integrity at risk.

Laboratory workflows demand precision, reliability, and compliance. The Cubis® II balance, combined with Sartorius’ powerful QApp software solutions, helps you achieve exactly that.

Discover how image-based automation tools like CellCelector streamline single-cell isolation, boost productivity, and improve research outcomes. Download the free Sartorius ebook now.

Unlock the secrets to high-performing cell cultures with our comprehensive eBook, Mastering Advanced Cell Cultures.

The Ph.Eur. Chapter 2.1.7 specifies mandatory requirements for analytical balances, including calibration, performance testing and minimum sample weight.

The Ph.Eur. Chapter 2.1.7 specifies mandatory requirements for analytical balances, including calibration, performance testing and minimum sample weight.

Understanding and adhering to the new ISO 8655:2022 standards is critical for laboratories working with piston-operated volumetric apparatus (POVA).

Stay ahead in your lab operations with our comprehensive guide to ISO 8655:2022-compliant pipette calibration. This resource is designed to help labs effectively manage, perform, and maintain accurate calibration procedures while adhering to strict regulatory standards.

In biopharmaceutical and life science research, accuracy and reproducibility are non-negotiable.

Maintaining data integrity is critical for labs in today's regulatory environment. Non-compliance can result in costly delays, product recalls, and reputation risks. With our Data Integrity Compliance Checklist, you can:

Phenotypic screening, which measures defined changes in cellular phenotype in response to a multitude of compounds, is essential in early-stage drug discovery.

Modern Requirements for Laboratory Balances

As the foundation for successful cell-based experiments, high-quality cell culture media directly impacts cell health, growth, and experimental reproducibility.

Regulatory requirements for laboratory balances used in pharmaceutical analysis have undergone significant updates across major pharmacopoeias over the last years

Designed to better mimic human biology, NAMs promise improved predictive accuracy for disease models, offering more relevant insights into human health.

With completely configurable hardware, software, and connectivity, Cubis® II and Cubis® II High-Resolution offer a high-performance balance that will align with your unique demands and compliance requirements.