Used ILLUMINA MiSeq #293598228 for sale

ILLUMINA MiSeq is a powerful research tool used for next-generation sequencing (NGS) in laboratory settings. It has been developed to support the latest advances in DNA sequencing technology, and the resulting data can be used for a variety of applications, including metagenomics, gene expression profiling, genotyping, and characterizing epigenetic features. By using paired-end and single-read sequencing, MiSeq can accurately read millions of DNA strands simultaneously. ILLUMINA MiSeq boasts a sample-to-answer workflow, meaning it can take samples directly from its instrument once they have been pre-run. MiSeq can process up to 12 samples at a time, allowing for a rapid and efficient process. It has an integrated flow cell and sequencing reagent, meaning it can produce sequencing results almost immediately after the DNA samples are loaded. ILLUMINA MiSeq is capable of sequencing to a read length of up to 2x150bp, and its wide range breadth allows for data to be generated using both single-end and paired-end data. In terms of accuracy and speed, MiSeq has the capability to generate data in the range of 2-3 million reads per hour. This can generate up to 15 gigabases of sequence data per run, offering powerful data crunching capabilities to researchers. Furthermore, ILLUMINA MiSeq is also compatible with microbial SNP genotyping and amplicon sequencing, making it suitable for a variety of research applications. More specifically, MiSeq is equipped with a high-quality system of internal optics, electronics, and software, which allow for easy and efficient data collection. ILLUMINA MiSeq also features a software package called MiSeq Reporter, which allows for convenient data storage and management. Additionally, ILLUMINA MiSeq boasts a superior data storage capacity, offering up to 4 billion bytes in memory. In conclusion, MiSeq has been designed to be a reliable and robust tool for research laboratories. It is easy to use, offers fast sequencing speeds, and is highly accurate. Furthermore, the compatibility with amplicon sequencing and SNP genotyping make this platform a versatile tool for modern research laboratories.