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Apps Android Apps iOS Apps Web Apps contact Ordering Information Troubleshooting Guide FAQ Quality & Safety Data GHS Hazard Labeling Certificates of Analysis Protein Crystallization Safety Data Sheets Quality Assurance Order Support Contact Customer Care Ordering Information Technical Support Contact by Web Form Contact by Phone or Fax About Us What We Do Who We Are Insights Magazine Sustainability Global Presence Social Hub Investor Relations At a Glance Share Information Analysts Financial Reports Events & Presentations Corporate Governance Compliance & Ethics IR Contacts Newsroom Press Releases Press Resources Photo Archive Video Footage Press Contact Contacts Price Inquiries Price Inquiries Technical Inquiries Global Contacts Meetings Subscribe to eNews Corporate Contacts What We Do Our Products Our Markets & Customers Innovation at QIAGEN Where We Are What We Offer Collaborative Culture Social Environment Career Paths Career Development & Training Compensation & Benefits Who We Are Facts & Figures History Management Awards & Recognitions Why QIAGEN Our Mission, Vision, Strategy Our Values Molecular Biology Revolution Outreach Programs Sustainability Diversity Meet Our People Overcoming Limitations in Quantitative, Multiplex Real-Time PCR Print Bookmark Share more.. Multiplex, real-time PCR is a powerful tool for gene expression analysis, viral load monitoring, genotyping, and many other applications. The ability to amplify and detect several genomic DNA, cDNA, or RNA targets in the same reaction vessel offers many benefits: Conservation of precious samples — more quantification data per sample Increased throughput — more targets analyzed per run on a cycler Reliable results — no well-to-well variability due to coamplification of internal control Reduced reagent costs — amplification of multiple targets in one reaction vessel Multiplex, real-time PCR is a powerful tool for gene expression analysis, viral load monitoring, genotyping, and many other applications. The ability to amplify and detect several genomic DNA, cDNA, or RNA targets in the same reaction vessel offers many benefits: Conservation of precious samples — more quantification data per sample Increased throughput — more targets analyzed per run on a cycler Reliable results — no well-to-well variability due to coamplification of internal control Reduced reagent costs — amplification of multiple targets in one reaction vessel Hide details Dr. Andreas Missel Dr. Missel is Director of Research and Development at QIAGEN, responsible for the development of modification and amplification technologies and products, such as reagents and assays for QIAGEN's standard and real-time PCR, RT-PCR, and HRM solutions. Dr. Missel received his PhD from the Gene Center at the University of Munich in molecular biology and biochemistry. He has been involved in various capacities in the biotechnology industry for more than 13 years. Dr. Missel is Director of Research and Development at QIAGEN, responsible for the development of modification and amplification technologies and products, such as reagents and assays for QIAGEN's standard and real-time PCR, RT-PCR, and HRM solutions. Dr. Missel received his PhD from the Gene Center at the University of Munich in molecular biology and biochemistry. He has been involved in various capacities in the biotechnology industry for more than 13 years. Hide details Contact QIAGEN Global contacts Technical Service Customer Care QIAGEN Apps Apps for your mobile devices! 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Overcoming Limitations in Quantitative, Multiplex Real-Time PCR

Multiplex, real-time PCR is a powerful tool for gene expression analysis, viral load monitoring, genotyping, and many other applications. The ability to amplify and detect several genomic DNA, cDNA, or RNA targets in the same reaction vessel offers many benefits:

Conservation of precious samples — more quantification data per sample
Increased throughput — more targets analyzed per run on a cycler
Reliable results — no well-to-well variability due to coamplification of internal control
Reduced reagent costs — amplification of multiple targets in one reaction vessel

Dr. Andreas Missel

Dr. Missel is Director of Research and Development at QIAGEN, responsible for the development of modification and amplification technologies and products, such as reagents and assays for QIAGEN's standard and real-time PCR, RT-PCR, and HRM solutions. Dr. Missel received his PhD from the Gene Center at the University of Munich in molecular biology and biochemistry. He has been involved in various capacities in the biotechnology industry for more than 13 years.

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