Used ILLUMINA NextSeq 500 #9408922 for sale

ILLUMINA NextSeq 500 is a high-throughput sequencing instrument from ILLUMINA that can produce sequencing data from a range of sample types. NextSeq 500 offers a wide range of configurability for different sequencing applications, including whole genome sequencing, RNA sequencing, epigenetics, and single cell sequencing. The equipment is capable of generating up to 1.14 billion ILLUMINA reads in a single run with a maximum of 480 samples on board. ILLUMINA NextSeq 500 system uses ILLUMINA sequencers, which are renowned for their accuracy, high quality data, and versatility. The unit combines two-channel flow cell technology with new sequencing chemistry to enable rapid and efficient data generation. This chemistry can produce both single-end and paired-end reads with lengths up to 250 bp, as well as longer reads up to 10 kb. The machine is suitable for both small- and large-scale sequencing experiments. NextSeq 500 tool also offers flexibility in terms of library preparation. It can handle both non-modular and modular library preparation reagents, enabling a wide range of sample types to be used for sequencing. ILLUMINA NextSeq 500 also features both a 3.5 hour data transfer time and an automated data analysis platform. It is connected to ILLUMINA BaseSpace Sequence Hub for real-time data analysis, eliminating the need for complex post-run data processing. This allows for data to be quickly transferred and analyzed, thus enabling faster decision-making in research studies. ILLUMINA Sequencing Asset has passed through rigorous testing and meets sequencing quality standards set by the International Requirements for Biomedical Technologies (IRBT). The model is also EMC certified, meaning it meets safety and regulatory requirements, thus making it suitable for all laboratory environments. Overall, NextSeq 500 offers excellent sequencing results, flexibility, and rapid data transfer and analysis. It is ideal for state-of-the-art sequencing applications including whole genome sequencing, RNA sequencing, epigenetics and single cell sequencing, to provide reliable and accurate data for various research studies.