*Please click here for service lab options as all kit orders for this method are currently being fulfilled by our service lab team.
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.
LoopSeq™ Bacterial Genome - Metagenomics 3x8-plex Kit
$100 to any US desitination
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