QIAGEN Life SciencesOvjeren akaunt

@QIAGENscience

Learn more about Sample to Insight solutions for PCR/qPCR, NGS and automation in life sciences. Visit

Hilden, Germany
Vrijeme pridruživanja: ožujak 2009.

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  1. Make 2020 the year of RNA-seq success with our ingenious FastSelect combos. Save >60% on your library prep & cut down workflow time by 44%. Learn more ⬇️

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  2. Interested in our live discussion on Feb 4 about how to analyze CTCs, EVs and ccfDNA in one blood sample? Join the QIAGEN Cancer Research Community and save a virtual seat ➡️

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  3. Got thousands of library prep samples but short on time? Automate to accelerate using our FX library prep workflow on the Hamilton NGS STAR platform. Uncover the benefits in this app note ⬇️

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  4. Multiply your efficiency with Multimodal Panels. One sample, one workflow, one day is all you need to detect DNA variants & RNA fusions simultaneously. Learn more ➡️

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  5. Whether you’re transitioning from qPCR or planning to switch from other technologies of dPCR, this nanoplate-based system will transform your experience. Watch the video ➡️

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  6. Jump from generating data to accumulating insights, with ease and speed. Our DNA panels now integrate bioinformatics software in a single kit. We’ve got your entire targeted NGS workflow covered ⬇️

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  7. Take a deep dive into the power of partitioning and application of digital PCR in the fields of rare target detection, CNV detection and validation of NGS results. Join us at the Festival of Genomics in London, Jan 28–30. ⬇️

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  8. Automating library prep can save time, minimize bias & increase reproducibility. Leverage the benefits by opting for our FX library prep workflow, which is automatable on the Hamilton NGS STAR platform. Download the app note for details ⬇️

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  9. Join us on January 16 to discover a new rRNA removal alternative to Ribo-Zero and RiboErase for bacterial and mammalian . Find out how this technology maximizes unique reads in RNA-seq. Register for webinar ➡️

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  10. Dr. Rob Philibert explains the benefits of using and the future of precision medicine. Check out his interview here ➡️

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  11. Vous souhaitez vous lancer dans le RNAseq ? Alors pensez QIAseq ! Rencontrez l’équipe QIAGEN aux 10èmes Assises de Génétique Humaine et Médicale afin de trouver la solution technique la plus adaptée à votre projet ➡️

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  12. From a limited sample, you can decipher intricate transcriptomic details. UPX 3’ Kits ensure precision, eliminate PCR bias & allow you to consolidate lots of libraries into a single sequencing lane to simplify gene expression RNA-seq ➡️

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  13. Save time and reagent costs by running a single, consolidated workflow for DNA and RNA profiling. Contact us to see how to integrate simultaneous detection of both DNA & RNA biomarkers into your lab ➡️

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  14. Antisense LNA GapmeRs are an excellent choice for gene silencing in animal models and cell cultures. But do you know why? Test your knowledge on this subject here ➡️

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  15. Think you’ve missed any of our expert webinars from the past year? Here’s another chance to view the on-demand recordings ➡️

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  16. Goodbye rRNA, hello unique reads. With the best ribosomal RNA removal technology you'll increase unique gene reads, from mammalian samples to complex bacterial environmental samples. Learn more ➡️

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  17. Check out the recorded webinars to discover a revolutionary technology that can ensure consistent, high-quality reads in RNA-seq with mammalian and bacterial samples ➡️

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  18. Trusted by researchers for more than 10 years, supports your research from idea exploration to analysis and follow-up. Get to know GeneGlobe – your design and analysis hub ➡️

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  19. New application note on GeneMarkerHID is now available. Learn how to improve analysis efficiency and rework of low-quality samples with automated Quality Sensor flagging in the software ➡️

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  20. Increase reliability and performance of PCR-based analyses. Watch our on-demand webinar ➡️

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