Nextera XT Index Kit

Nextera XT Index Kit

Illumina/Nextera XT Index Kit v2 Set D (96 indexes, 384 samples)/FC-131-2004/1 Ea

產品編號： FC-131-2004

美  元  價： $989.00

品       牌： Illumina

產       地： 美國

公       司： Illumina, Inc

Product Highlights:

Fast Library Prep, Optimized for Small Genomes, PCR Amplicons, and Plasmids

Rapid library preparation – complete library prep in as little as 90 minutes with only 15 minutes of hands-on time

Fast time to results – go from DNA to data in 8 hours with our benchtop sequencers.

Optimized for small genomes, PCR amplicons, and plasmids – one library prep kit for many applications

Innovative sample normalization – eliminates the need for library quantification before sample pooling and sequencing

With Nextera technology, DNA is simultaneously fragmented and tagged with sequencing adapters in a single tube enzymatic reaction. Nextera XT supports ultra-low DNA input of only 1 ng. It enables a wide range of input samples, including small genomes, PCR amplicons greater than 300 bp, plasmids, microbial genomes, concatenated amplicons, and double-stranded CDNA.

Multiplexing of up to 384 samples per Nextera XT library is also available for those projects requiring greater throughput. Plus, the kit includes an innovative bead-based sample normalization that eliminates the need for library quantification prior to pooling and sequencing. Libraries prepared with Nextera XT kits are compatIBLe with all Illumina sequencers.

Find an up-to-date list of high-throughput automation vendors with robotic systems compatIBLe with this library preparation kit

Specifications:

Assay Time 90 minutes

Hands-On Time 15 minutes

Mechanism of Action Enzymatic Fragmentation

Multiplexing Up to 384 uniquely indexed samples may be pooled and sequenced together.

Input Quantity 1 ng DNA

Species Category Drosophila,Any Species,Mammalian,Mouse,Yeast,Zebrafish,Human,Rat,Plant,Nematode,Bacteria

System Compatibility MiSeq,NextSeq 550,NextSeq 500,MiSeq FGx in Research Mode

Method Shotgun Sequencing,Whole-Genome Sequencing,De Novo Sequencing,16S rRNA Sequencing,Amplicon Sequencing,Targeted DNA Sequencing

Variant Class Single Nucleotide Polymorphisms (SNPs),Structural Variants

Specialized Sample Types Low Input,Single Cells

Technology Sequencing