Assay design & validation for gene expression & SNP genotyping [AB5-0518]
Event Information
Description
Design and validation of your qPCR assays is key to successfully producing high-quality data. Good design also saves both time and money.
During this seminar, co-organized by TATAA Biocenter AB and Integrated DNA Technologies (IDT), you will learn about the workflow for proper assay design and validation.
We will focus on the tools that help you achieve relevance, accuracy, correct interpretation and repeatability, how to design and wet-lab validate your assays as well which controls you need to include.
Featured products:
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PrimeTime qPCR predesigned assays for human, mouse and rat. These assays are synthesized using current sequence information and have guaranteed performance.
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Double-Quenched ZEN probes have consistently low background, reduced C q values, improved precision, and enable the use of longer probes.
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IDT has used the rhPCR technology to develop a superior SNP discrimination system: rhAmp SNP Genotyping. The system increases the signal-to-noise ratios and leads to improved cluster separation and higher confidence genotyping calls.
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gBlock Gene Fragments are sequence-verified, double-stranded DNA fragments for affordable and easy qPCR standards.
Speakers:
Prof. Mikael Kubista, Founder of TATAA Biocenter AB
Dr. Richelle Spanjers, Field Application Specialist qPCR & Genotyping, IDT