Electrophoresis Market by Product (Consumables, Equipment, Services), Application (Clinical Diagnostics, Forensics, Pharmaceutical), End User - Global Forecast 2025-2032
Description
The Electrophoresis Market was valued at USD 3.47 billion in 2024 and is projected to grow to USD 3.68 billion in 2025, with a CAGR of 6.37%, reaching USD 5.69 billion by 2032.
A concise primer on modern electrophoresis trends technological drivers and strategic imperatives shaping laboratory workflows and innovation pathways
Electrophoresis remains a foundational laboratory technique whose continuous evolution influences diagnostics, forensic workflows, pharmaceutical development, and basic life sciences research. In recent years, incremental improvements in gel chemistries and instrument precision have converged with digital imaging, automation, and software analytics to extend the utility of electrophoretic separation beyond traditional use cases. This introduction sets the context for understanding how technological advances, supply chain dynamics, regulatory pressures, and end-user expectations together shape procurement priorities and laboratory practices.
The narrative begins by framing electrophoresis as both a core analytical method and a platform for innovation. It then traces how adjacent innovations-such as improvements in consumable chemistry, miniaturized and capillary-based equipment, and integrated data management-have created new value propositions for clinical and research laboratories. Finally, the introduction highlights the strategic questions executives must address: how to balance capital and consumable investment, how to validate new workflows within regulatory constraints, and how to secure supply continuity in an increasingly complex global ecosystem. This sets the stage for deeper analysis of shifting technologies, tariff impacts, segmentation-specific dynamics, and recommended strategic responses.
Transformative technological shifts in electrophoresis platforms automation digital integration and reagent design that are redefining laboratory efficiency and analytical precision
The landscape of electrophoresis is undergoing transformative shifts driven by a blend of technological maturation and changing operational priorities. Advances in automation and digital integration have reduced hands-on time and minimized variability while enabling higher throughput and reproducibility. Concurrently, improvements in consumable design-ranging from optimized buffer formulations to pre-cast gels and kit-based workflows-have simplified assay setup and supported adoption in regulated environments.
Moreover, the adoption of capillary electrophoresis and pulsed-field techniques has expanded analytical capabilities, enabling laboratories to separate complex biomolecules with greater resolution. Software innovations that automate image analysis, support cloud-based data management, and integrate with laboratory information systems are enhancing data traceability and facilitating compliance. At the same time, user expectations are shifting toward turnkey solutions that combine reliable equipment, validated consumables, and responsive service models. Collectively, these shifts are lowering technical barriers for non-specialist users, creating new competitive dynamics among suppliers, and prompting strategic reassessment of procurement, training, and validation processes across clinical, forensic, pharmaceutical, and research settings.
Analysis of cumulative effects of United States tariff policy changes on electrophoresis supply chains component sourcing logistics and laboratory procurement resilience
Recent tariff measures enacted in the United States have introduced new layers of complexity to electrophoresis supply chains, affecting component sourcing, manufacturing economics, and procurement decisions. Tariffs on imported instrument components and certain reagent precursors have increased landed costs for some suppliers, prompting re-evaluation of supplier networks and encouraging onshore manufacturing or near-shoring strategies where feasible. These adjustments, in turn, have influenced lead times and inventory planning for laboratories that depend on consistent availability of consumables and parts.
In response, many suppliers have adopted a range of mitigation tactics including diversifying their supplier base, negotiating long-term purchase agreements, and increasing buffer inventory for critical items. Procurement teams are placing greater emphasis on supply chain transparency and supplier financial resilience when qualifying new vendors. For end users, the tariff environment has reinforced the importance of validating alternative consumables and establishing contingency plans to avoid workflow disruptions. Looking ahead, organizations that proactively assess supplier risk, optimize inventory policies, and prioritize suppliers with resilient logistics capabilities will be better positioned to navigate ongoing tariff-driven volatility while maintaining uninterrupted laboratory operations.
Segment-specific insights linking product portfolios application demands and end-user expectations to commercialization levers and adoption barriers across electrophoresis
A nuanced understanding of segmentation is essential to navigate product development, commercialization priorities, and service delivery in electrophoresis. Based on product, the market is studied across Consumables, Equipment, Services, and Software; the Consumables category further breaks down across Buffers, Gels, Kits, and Reagents while Equipment spans Agarose Gel, Capillary, Polyacrylamide Gel, and Pulsed Field platforms. These product distinctions matter because consumables drive recurring revenue streams and user lock-in through validated kits and reagent systems, whereas equipment choices determine capital expenditure profiles, laboratory footprint, and the degree of automation a workflow can support.
Based on application, the market is studied across Clinical Diagnostics, Forensics, Pharmaceutical, and Research, and each application imposes distinct requirements on validation, traceability, and result interpretability. Clinical diagnostics and pharmaceutical applications typically demand stringent quality systems and batch traceability, whereas research and forensic contexts may prioritize resolution, sensitivity, and chain-of-custody considerations. Based on end user, the market is studied across Academic & Research Institutes, Forensic Laboratories, Hospitals & Diagnostic Laboratories, and Pharmaceutical & Biotechnology Companies, and each end-user segment exhibits unique purchasing cycles, budget constraints, and adoption drivers. Taken together, these segmentation lenses highlight where suppliers should focus product development, regulatory support, and field service capabilities to align with the differentiated needs of each customer cohort.
Regional strategic outlook identifying how the Americas Europe Middle East & Africa and Asia-Pacific diverge in adoption drivers regulatory nuances and supply chain priorities
Regional dynamics play a decisive role in technology adoption, regulatory alignment, and supply chain design for electrophoresis. In the Americas, purchasing decisions are often influenced by large integrated health systems and a mature network of service providers that support rapid instrument deployment and consumable restocking. This environment favors suppliers that can demonstrate robust service coverage, regulatory compliance support, and scalable training programs to meet decentralized laboratory needs.
Europe, Middle East & Africa presents a heterogeneous landscape where regulatory frameworks vary widely and reimbursement pathways are a key determinant of adoption, particularly in clinical diagnostics. Suppliers that can provide clear compliance documentation, multilingual technical support, and flexible logistics solutions tend to gain competitive advantage. In the Asia-Pacific region, rapid investments in research infrastructure and growing pharmaceutical manufacturing capacity are driving demand for advanced separation technologies, but price sensitivity and local manufacturing capabilities influence procurement strategies. Across all regions, supply chain resilience, local regulatory expertise, and tailored commercial models are critical success factors that should guide regional go-to-market planning and partnership selection.
Competitive company dynamics and innovation strategies illuminating partnerships product differentiation manufacturing footprints and service models that drive industry leadership
Competitive dynamics among companies in the electrophoresis space are characterized by a blend of product innovation, strategic partnerships, and differentiated service models. Leading players tend to invest in consumable ecosystems that lock in recurring revenue while offering instruments engineered for reliability and ease of validation. Strategic collaborations with reagent manufacturers, software developers, and academic centers enable faster validation cycles and broader application coverage, supporting deeper penetration into regulated environments.
Additionally, companies are optimizing manufacturing footprints to balance cost efficiency with supply resilience, and they are increasingly leveraging contract manufacturing and regional distribution partnerships to shorten lead times. Intellectual property around gel chemistries, capillary technologies, and image-analysis algorithms remains a competitive asset, and organizations that effectively bundle hardware, consumables, and software support a superior total-cost-of-ownership proposition for end users. In parallel, service excellence-measured by response times, training quality, and validation support-continues to differentiate suppliers in procurement decisions where uptime and compliance are paramount.
Actionable strategic recommendations for industry leaders to strengthen supply resilience accelerate commercialization and align product development with evolving laboratory priorities
Industry leaders should pursue a set of actionable initiatives to strengthen market position, mitigate operational risk, and accelerate value delivery to customers. First, prioritize the development of integrated consumable and instrument systems that simplify validation and reduce operator variability, thereby appealing to regulated laboratories that value turnkey solutions. Secondly, invest in supply chain transparency by qualifying multiple suppliers for critical components, implementing risk-scoring frameworks, and maintaining safety stock where appropriate to reduce vulnerability to tariff shocks and logistics disruptions.
Third, enhance digital capabilities by embedding analytics and secure data exchange into instrument offerings so that customers can extract more actionable information from separations while meeting data integrity requirements. Fourth, expand service and training footprints with regionally tailored programs that address local regulatory and language needs, thereby shortening time-to-value for new customers. Fifth, pursue strategic partnerships with academic and clinical centers to co-develop workflows and generate independent performance validation. Finally, adopt flexible commercial models, including subscription and consumable-based pricing, to align supplier incentives with customer outcomes and to facilitate smoother procurement paths for budget-constrained end users.
Transparent research methodology combining primary interviews laboratory audits supply chain mapping and quantitative triangulation to ensure robust actionable sector insights
This analysis is grounded in a mixed-methods research approach that combines primary qualitative engagement with quantitative data triangulation to ensure robust and actionable insights. Primary research included structured interviews with laboratory directors, procurement executives, and technical staff across clinical, forensic, pharmaceutical, and academic settings, complemented by supplier discussions focusing on manufacturing, logistics, and product roadmaps. These interviews were supplemented by site visits and audits to observe workflow integration, instrument utilization patterns, and consumable handling practices.
Secondary research incorporated peer-reviewed literature, regulatory guidance documents, patent filings, and supplier technical documentation to validate technological claims and to contextualize product performance. Analytical techniques included supply chain mapping to identify chokepoints and scenario analysis to test the resilience of procurement strategies under tariff-induced stress. Throughout the methodology, rigorous data quality checks and cross-validation were applied to reconcile discrepancies and to ensure that conclusions are supported by multiple evidence streams. This transparent methodology supports reproducibility and provides a defensible basis for the strategic recommendations presented.
Concluding synthesis that distills technological regulatory and commercial priorities into clear guidance for executive decision-making in electrophoresis operations
In conclusion, electrophoresis continues to be a vital and adaptive technology platform that benefits from concurrent advances in consumable chemistry, instrument design, and digital analytics. The interplay of these advances is enabling broader adoption across clinical, forensic, pharmaceutical, and research applications by simplifying workflows and improving data quality. At the same time, external pressures such as tariff changes and regional regulatory heterogeneity are reshaping supply chain strategies and procurement priorities, underscoring the importance of resilience and supplier transparency.
Executives and technical leaders should focus on integrated solutions that pair validated consumables with user-friendly instruments and powerful analytics, while also investing in service capabilities and regional compliance expertise. By aligning R&D, commercial, and operational strategies with differentiated end-user needs and regional realities, organizations can capture the value created by technological innovation while minimizing disruption from policy-driven supply chain shifts. The insights in this executive summary are intended to guide informed decision-making and to catalyze practical steps that strengthen competitive positioning and operational continuity across electrophoresis applications.
Please Note: PDF & Excel + Online Access - 1 Year
A concise primer on modern electrophoresis trends technological drivers and strategic imperatives shaping laboratory workflows and innovation pathways
Electrophoresis remains a foundational laboratory technique whose continuous evolution influences diagnostics, forensic workflows, pharmaceutical development, and basic life sciences research. In recent years, incremental improvements in gel chemistries and instrument precision have converged with digital imaging, automation, and software analytics to extend the utility of electrophoretic separation beyond traditional use cases. This introduction sets the context for understanding how technological advances, supply chain dynamics, regulatory pressures, and end-user expectations together shape procurement priorities and laboratory practices.
The narrative begins by framing electrophoresis as both a core analytical method and a platform for innovation. It then traces how adjacent innovations-such as improvements in consumable chemistry, miniaturized and capillary-based equipment, and integrated data management-have created new value propositions for clinical and research laboratories. Finally, the introduction highlights the strategic questions executives must address: how to balance capital and consumable investment, how to validate new workflows within regulatory constraints, and how to secure supply continuity in an increasingly complex global ecosystem. This sets the stage for deeper analysis of shifting technologies, tariff impacts, segmentation-specific dynamics, and recommended strategic responses.
Transformative technological shifts in electrophoresis platforms automation digital integration and reagent design that are redefining laboratory efficiency and analytical precision
The landscape of electrophoresis is undergoing transformative shifts driven by a blend of technological maturation and changing operational priorities. Advances in automation and digital integration have reduced hands-on time and minimized variability while enabling higher throughput and reproducibility. Concurrently, improvements in consumable design-ranging from optimized buffer formulations to pre-cast gels and kit-based workflows-have simplified assay setup and supported adoption in regulated environments.
Moreover, the adoption of capillary electrophoresis and pulsed-field techniques has expanded analytical capabilities, enabling laboratories to separate complex biomolecules with greater resolution. Software innovations that automate image analysis, support cloud-based data management, and integrate with laboratory information systems are enhancing data traceability and facilitating compliance. At the same time, user expectations are shifting toward turnkey solutions that combine reliable equipment, validated consumables, and responsive service models. Collectively, these shifts are lowering technical barriers for non-specialist users, creating new competitive dynamics among suppliers, and prompting strategic reassessment of procurement, training, and validation processes across clinical, forensic, pharmaceutical, and research settings.
Analysis of cumulative effects of United States tariff policy changes on electrophoresis supply chains component sourcing logistics and laboratory procurement resilience
Recent tariff measures enacted in the United States have introduced new layers of complexity to electrophoresis supply chains, affecting component sourcing, manufacturing economics, and procurement decisions. Tariffs on imported instrument components and certain reagent precursors have increased landed costs for some suppliers, prompting re-evaluation of supplier networks and encouraging onshore manufacturing or near-shoring strategies where feasible. These adjustments, in turn, have influenced lead times and inventory planning for laboratories that depend on consistent availability of consumables and parts.
In response, many suppliers have adopted a range of mitigation tactics including diversifying their supplier base, negotiating long-term purchase agreements, and increasing buffer inventory for critical items. Procurement teams are placing greater emphasis on supply chain transparency and supplier financial resilience when qualifying new vendors. For end users, the tariff environment has reinforced the importance of validating alternative consumables and establishing contingency plans to avoid workflow disruptions. Looking ahead, organizations that proactively assess supplier risk, optimize inventory policies, and prioritize suppliers with resilient logistics capabilities will be better positioned to navigate ongoing tariff-driven volatility while maintaining uninterrupted laboratory operations.
Segment-specific insights linking product portfolios application demands and end-user expectations to commercialization levers and adoption barriers across electrophoresis
A nuanced understanding of segmentation is essential to navigate product development, commercialization priorities, and service delivery in electrophoresis. Based on product, the market is studied across Consumables, Equipment, Services, and Software; the Consumables category further breaks down across Buffers, Gels, Kits, and Reagents while Equipment spans Agarose Gel, Capillary, Polyacrylamide Gel, and Pulsed Field platforms. These product distinctions matter because consumables drive recurring revenue streams and user lock-in through validated kits and reagent systems, whereas equipment choices determine capital expenditure profiles, laboratory footprint, and the degree of automation a workflow can support.
Based on application, the market is studied across Clinical Diagnostics, Forensics, Pharmaceutical, and Research, and each application imposes distinct requirements on validation, traceability, and result interpretability. Clinical diagnostics and pharmaceutical applications typically demand stringent quality systems and batch traceability, whereas research and forensic contexts may prioritize resolution, sensitivity, and chain-of-custody considerations. Based on end user, the market is studied across Academic & Research Institutes, Forensic Laboratories, Hospitals & Diagnostic Laboratories, and Pharmaceutical & Biotechnology Companies, and each end-user segment exhibits unique purchasing cycles, budget constraints, and adoption drivers. Taken together, these segmentation lenses highlight where suppliers should focus product development, regulatory support, and field service capabilities to align with the differentiated needs of each customer cohort.
Regional strategic outlook identifying how the Americas Europe Middle East & Africa and Asia-Pacific diverge in adoption drivers regulatory nuances and supply chain priorities
Regional dynamics play a decisive role in technology adoption, regulatory alignment, and supply chain design for electrophoresis. In the Americas, purchasing decisions are often influenced by large integrated health systems and a mature network of service providers that support rapid instrument deployment and consumable restocking. This environment favors suppliers that can demonstrate robust service coverage, regulatory compliance support, and scalable training programs to meet decentralized laboratory needs.
Europe, Middle East & Africa presents a heterogeneous landscape where regulatory frameworks vary widely and reimbursement pathways are a key determinant of adoption, particularly in clinical diagnostics. Suppliers that can provide clear compliance documentation, multilingual technical support, and flexible logistics solutions tend to gain competitive advantage. In the Asia-Pacific region, rapid investments in research infrastructure and growing pharmaceutical manufacturing capacity are driving demand for advanced separation technologies, but price sensitivity and local manufacturing capabilities influence procurement strategies. Across all regions, supply chain resilience, local regulatory expertise, and tailored commercial models are critical success factors that should guide regional go-to-market planning and partnership selection.
Competitive company dynamics and innovation strategies illuminating partnerships product differentiation manufacturing footprints and service models that drive industry leadership
Competitive dynamics among companies in the electrophoresis space are characterized by a blend of product innovation, strategic partnerships, and differentiated service models. Leading players tend to invest in consumable ecosystems that lock in recurring revenue while offering instruments engineered for reliability and ease of validation. Strategic collaborations with reagent manufacturers, software developers, and academic centers enable faster validation cycles and broader application coverage, supporting deeper penetration into regulated environments.
Additionally, companies are optimizing manufacturing footprints to balance cost efficiency with supply resilience, and they are increasingly leveraging contract manufacturing and regional distribution partnerships to shorten lead times. Intellectual property around gel chemistries, capillary technologies, and image-analysis algorithms remains a competitive asset, and organizations that effectively bundle hardware, consumables, and software support a superior total-cost-of-ownership proposition for end users. In parallel, service excellence-measured by response times, training quality, and validation support-continues to differentiate suppliers in procurement decisions where uptime and compliance are paramount.
Actionable strategic recommendations for industry leaders to strengthen supply resilience accelerate commercialization and align product development with evolving laboratory priorities
Industry leaders should pursue a set of actionable initiatives to strengthen market position, mitigate operational risk, and accelerate value delivery to customers. First, prioritize the development of integrated consumable and instrument systems that simplify validation and reduce operator variability, thereby appealing to regulated laboratories that value turnkey solutions. Secondly, invest in supply chain transparency by qualifying multiple suppliers for critical components, implementing risk-scoring frameworks, and maintaining safety stock where appropriate to reduce vulnerability to tariff shocks and logistics disruptions.
Third, enhance digital capabilities by embedding analytics and secure data exchange into instrument offerings so that customers can extract more actionable information from separations while meeting data integrity requirements. Fourth, expand service and training footprints with regionally tailored programs that address local regulatory and language needs, thereby shortening time-to-value for new customers. Fifth, pursue strategic partnerships with academic and clinical centers to co-develop workflows and generate independent performance validation. Finally, adopt flexible commercial models, including subscription and consumable-based pricing, to align supplier incentives with customer outcomes and to facilitate smoother procurement paths for budget-constrained end users.
Transparent research methodology combining primary interviews laboratory audits supply chain mapping and quantitative triangulation to ensure robust actionable sector insights
This analysis is grounded in a mixed-methods research approach that combines primary qualitative engagement with quantitative data triangulation to ensure robust and actionable insights. Primary research included structured interviews with laboratory directors, procurement executives, and technical staff across clinical, forensic, pharmaceutical, and academic settings, complemented by supplier discussions focusing on manufacturing, logistics, and product roadmaps. These interviews were supplemented by site visits and audits to observe workflow integration, instrument utilization patterns, and consumable handling practices.
Secondary research incorporated peer-reviewed literature, regulatory guidance documents, patent filings, and supplier technical documentation to validate technological claims and to contextualize product performance. Analytical techniques included supply chain mapping to identify chokepoints and scenario analysis to test the resilience of procurement strategies under tariff-induced stress. Throughout the methodology, rigorous data quality checks and cross-validation were applied to reconcile discrepancies and to ensure that conclusions are supported by multiple evidence streams. This transparent methodology supports reproducibility and provides a defensible basis for the strategic recommendations presented.
Concluding synthesis that distills technological regulatory and commercial priorities into clear guidance for executive decision-making in electrophoresis operations
In conclusion, electrophoresis continues to be a vital and adaptive technology platform that benefits from concurrent advances in consumable chemistry, instrument design, and digital analytics. The interplay of these advances is enabling broader adoption across clinical, forensic, pharmaceutical, and research applications by simplifying workflows and improving data quality. At the same time, external pressures such as tariff changes and regional regulatory heterogeneity are reshaping supply chain strategies and procurement priorities, underscoring the importance of resilience and supplier transparency.
Executives and technical leaders should focus on integrated solutions that pair validated consumables with user-friendly instruments and powerful analytics, while also investing in service capabilities and regional compliance expertise. By aligning R&D, commercial, and operational strategies with differentiated end-user needs and regional realities, organizations can capture the value created by technological innovation while minimizing disruption from policy-driven supply chain shifts. The insights in this executive summary are intended to guide informed decision-making and to catalyze practical steps that strengthen competitive positioning and operational continuity across electrophoresis applications.
Please Note: PDF & Excel + Online Access - 1 Year
Table of Contents
185 Pages
- 1. Preface
- 1.1. Objectives of the Study
- 1.2. Market Segmentation & Coverage
- 1.3. Years Considered for the Study
- 1.4. Currency
- 1.5. Language
- 1.6. Stakeholders
- 2. Research Methodology
- 3. Executive Summary
- 4. Market Overview
- 5. Market Insights
- 5.1. Increasing integration of microfluidic electrophoresis platforms for point-of-care diagnostics in personalized medicine
- 5.2. Expansion of high-throughput capillary electrophoresis systems to accelerate genomics and proteomics research workflows
- 5.3. Development of label-free fluorescent detection methods improving sensitivity in capillary electrophoresis clinical assays
- 5.4. Rising demand for lab-on-a-chip electrophoresis solutions enabling multiplexed analysis in environmental monitoring applications
- 5.5. Adoption of automated gel electrophoresis instruments to enhance reproducibility and throughput in pharmaceutical quality control processes
- 5.6. Growing collaborations between electrophoresis instrument manufacturers and AI developers for advanced data interpretation algorithms
- 6. Cumulative Impact of United States Tariffs 2025
- 7. Cumulative Impact of Artificial Intelligence 2025
- 8. Electrophoresis Market, by Product
- 8.1. Consumables
- 8.1.1. Buffers
- 8.1.2. Gels
- 8.1.3. Kits
- 8.1.4. Reagents
- 8.2. Equipment
- 8.2.1. Agarose Gel
- 8.2.2. Capillary
- 8.2.3. Polyacrylamide Gel
- 8.2.4. Pulsed Field
- 8.3. Services
- 8.4. Software
- 9. Electrophoresis Market, by Application
- 9.1. Clinical Diagnostics
- 9.2. Forensics
- 9.3. Pharmaceutical
- 9.4. Research
- 10. Electrophoresis Market, by End User
- 10.1. Academic & Research Institutes
- 10.2. Forensic Laboratories
- 10.3. Hospitals & Diagnostic Laboratories
- 10.4. Pharmaceutical & Biotechnology Companies
- 11. Electrophoresis Market, by Region
- 11.1. Americas
- 11.1.1. North America
- 11.1.2. Latin America
- 11.2. Europe, Middle East & Africa
- 11.2.1. Europe
- 11.2.2. Middle East
- 11.2.3. Africa
- 11.3. Asia-Pacific
- 12. Electrophoresis Market, by Group
- 12.1. ASEAN
- 12.2. GCC
- 12.3. European Union
- 12.4. BRICS
- 12.5. G7
- 12.6. NATO
- 13. Electrophoresis Market, by Country
- 13.1. United States
- 13.2. Canada
- 13.3. Mexico
- 13.4. Brazil
- 13.5. United Kingdom
- 13.6. Germany
- 13.7. France
- 13.8. Russia
- 13.9. Italy
- 13.10. Spain
- 13.11. China
- 13.12. India
- 13.13. Japan
- 13.14. Australia
- 13.15. South Korea
- 14. Competitive Landscape
- 14.1. Market Share Analysis, 2024
- 14.2. FPNV Positioning Matrix, 2024
- 14.3. Competitive Analysis
- 14.3.1. Thermo Fisher Scientific Inc.
- 14.3.2. Agilent Technologies, Inc.
- 14.3.3. Bio-Rad Laboratories, Inc.
- 14.3.4. Merck KGaA
- 14.3.5. Danaher Corporation
- 14.3.6. PerkinElmer, Inc.
- 14.3.7. Waters Corporation
- 14.3.8. GE HealthCare Technologies Inc.
- 14.3.9. Shimadzu Corporation
- 14.3.10. Bio-Techne Corporation
- 14.3.11. Sebia Group
- 14.3.12. Harvard Bioscience, Inc.
- 14.3.13. SERVA Electrophoresis GmbH
- 14.3.14. Cleaver Scientific Ltd.
- 14.3.15. Helena Laboratories Corporation
- 14.3.16. Analytik Jena AG
- 14.3.17. Takara Bio Inc.
- 14.3.18. Promega Corporation
- 14.3.19. Bio-Techne Corporation
- 14.3.20. Eppendorf SE
- 14.3.21. Hitachi High-Tech Corporation
- 14.3.22. New England Biolabs, Inc.
- 14.3.23. Lumex Instruments Canada Ltd.
- 14.3.24. Wyatt Technology Corporation
- 14.3.25. Hoefer, Inc.
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