DNA sequencing reagent kit LoopSeq™ Bacterial
for molecular biology

DNA sequencing reagent kit
DNA sequencing reagent kit
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for DNA sequencing, for molecular biology


This kit is for de novo bacterial genome sequencing and assembly or to deliver a comprehensive metagenomics survey and accurate relative abundance of many molecules in DNA samples. Single molecule long read data is generated as well as relative abundance using barcode based molecular counting. It also features a multiplex workflow that pools 24 samples into a single tube with less than 3 hours of hands-on time. It’s the perfect kit for labs looking to perform de novo bacterial genome assembly or for labs looking to get long-read Metagenomics data from any DNA samples they have. Compatible with all Illumina instruments.* *HiSeqs, NextSeqs, and NovaSeqs are recommended for per base cost benefits. Assay Time 8.5 hours Hands-On Time 2.5 hours Mechanism of Action Synthetic long read sequencing Multiplexing Allows for 24 samples to be processed in one tube Input Quantity 10 ng genomic DNA (2 ng/ul) Category any linear dsDNA input System Compatibility HiSeq 2500, HiSeq 3000, HiSeq 4000, NextSeq, NovaSeq, MiniSeq, MiSeq Nucleic Acid Type DNA Method 2 x 150 Paired End (PE) sequencing Specialized Sample Types PCR products, genomes, metagenomes, synthetic DNA libraries, viruses Technology Assembly of a synthetic long reads form short reads Automation Capability Yes The advantages of long-read sequencing. the convenience of your existing sequencing infrastructure Next generation sequencing (NGS) has been an incredibly powerful technique, but there are many applications where short-read sequencing comes up, well, short. Fortunately, Loop Genomics has developed an affordable


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*Prices are pre-tax. They exclude delivery charges and customs duties and do not include additional charges for installation or activation options. Prices are indicative only and may vary by country, with changes to the cost of raw materials and exchange rates.