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Benefit from more than 25 years of experience in oligonucleotide synthesis!
Optimise your research and save time with high quality gene synthesis and molecular biology services.
Hiqh quality Sanger sequencing with highest flexibility for every sample type.
NGS from experts - ISO-certified, fully automated and easy to order online.
Cell line authentication, Mycoplasmacheck, Fragment length analysis & tailored projects.
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Our genomics solutions support you along your drug development chain of small and large molecules and in precision medicine.
Benefit from our range of tailored, high throughput genotyping solutions to help you achieve your goals faster, for less.
Welcome to your full-service laboratory. Benefit from our end-to end solutions for sample collection kit logistics and genomic solutions.
DNA-based solutions to improve and support your analysis, monitoring and traceability across your value chain.
Our scalable and high-quality oligonucleotides synthesis offer makes us an ideal partner for your industry applications.
For your research project in academic, governmental and industrial environment we have the right genomic service.
Eurofins GenomicsGermany GmbHAnzinger Str. 7a85560 EbersbergGermany
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Dr. Melvin Siliakus
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Oligonucleotide Synthesis
Gene Synthesis & Molecular Biology
Next Generation Sequencing
Genotyping & Genexpression
Primers & Probes for qPCR Applications
Oligos for Next Generation Sequencing
Primers for Sanger Sequencing
Oligos for Cloning Applications
Custom Oligos
Oligo Tools
Synthetic genes
GeneStrands
Molecular Biology Services
Sanger Sequencing Services
Prepaid Products for Sanger Sequencing
Additional Services
Genome Sequencing
Transcriptome Sequencing
Metagenome / Microbiome
Exome Sequencing & Oncology Solutions
CRISPR & Prepaid NGS Coupons
VIRUS
Plasmid Sequencing
Amplicon sequencing & Ready-to-Load
Oxford Nanopore projects (WGS, Amplicons, 16S)
ONT Lite
Mycoplasmacheck
CLA & FLA
Others
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Nein, dies wird nicht empfohlen. Optimale Ergebnisse können erzielt werden, wenn die Fragmentierung direkt vor der Bibliotheksvorbereitung durchgeführt wird. Wir empfehlen, unfragmentierte HMW-DNA zu senden, möglichst groß.