Used ILLUMINA MiSeq #293621321 for sale

ILLUMINA MiSeq is a laboratory equipment and accessory used for sequencing a genome. It is a Next-Generation Sequencing (NGS) platform, used to perform various applications such as: Targeted Re-Sequencing, Exome Sequencing, Small RNA Sequencing, Whole Genome Sequencing and Metagenomics. MiSeq system provides flexibility to choose from a wide range of sequencing solutions and enables sequencing of both DNA and RNA, as well as sequencing of multiple samples in a single run. ILLUMINA MiSeq is a highly sensitive benchtop sequencer that works with real-time data and can be operated using a web-based solution (Sequencer Control Software). The sequencer is automated and offers throughput capabilities that range from 2 to 300 gigs of data per run. It is built with ILLUMINA proprietary sequencing-by-synthesis technology which has enabled longer reads and faster turnaround time for sequencing projects. MiSeq sequencer comes with a flow cell that can hold up to six sample wells, each with a capacity of up to 450 base pairs. The flow cell is equipped with laser optics, CCD cameras and sensors that work together to collect data from the DNA strands and convert it into electronic information during each run. This sequencer produces data in FASTQ format and comes with a range of optional accessories for sample prep and library creation. For efficient sequencing ILLUMINA MiSeq has to be coupled with the right mix of reagents including: sequencing kits, PCR primers, Shearase enzyme and DNA sample prep kits. The sequencing kits provide DNA sequencing primers and sequencing buffers as well as reagents for sequencing quality control. For library preparation, MiSeq also requires adapters and other prerequisites such as enzymes and polymerases. ILLUMINA MiSeq is a popular platform used by researchers and biomedical experts for the study of genetic diseases, cancer research, and other scientific investigations. MiSeq produces accurate and reliable data and provides insight into the complexity and diversity of genetic information. The information can then be used for precision medicine and drug development, as well as for personalized medical treatments.