Everything you need for PacBio sequencing.
Browse our collection of sample preparation kits, application kits, library prep and barcoding, and sequencing kits.
|Library Prep + Barcoding
Short Read Eliminator Kits:
SMRTbell Library Prep For Hifi Sequencing:
Onso Library Prep:
Discover new biology in your single-cell transcriptome studies with the MAS-seq kit. Obtain full-length isoform information at single-cell resolution by combining the power of single-cell technology from 10x Genomics with PacBio HiFi sequencing.
MAS-SEQ FOR 10X SINGLE CELL 3’ KIT
The MAS-Seq for 10x Single Cell 3’ kit containing oligos and reagents for making MAS-Seq libraries from cDNA generated using the 10x Chromium Next GEM Single Cell 3′ kit (v3.1). The kit contains MAS adapters that produces a library ready for sequencing.
HIFI SEQUENCING: REVIO CONSUMABLES
The Revio system simplifies the HiFi sequencing experience with fewer consumables optimized for easy tracking and minimal waste. With workflow improvements, loading consumables takes under a minute at the instrument.
REVIO POLYMERASE KIT
Optimized reagents to bind polymerase to prepare 24 SMRTbell libraries for sequencing
REVIO SMRT CELL TRAY
4 high-density SMRT Cells, each with 25 million ZMWs
REVIO SEQUENCING PLATE
Reagents for sequencing up to 4 Revio SMRT Cells. The sequencing plate combines multiple parts from the Sequel IIe system: sequencing plate, tube septa, sample plate, mixing plate, and SMRT Cell oil.
NANOBIND HMW DNA EXTRACTION
Micro-, nano-, and single-molecule technologies to streamline every step in the genomics workflow
SHORT READ ELIMINATOR KITS
Get rid of short DNA quickly and efficiently
SMRTbell prep kit 3.0 and Binding kits 3.1 and 3.2 accelerate sample preparation times, lower DNA input requirements, and simplify protocol guidance across applications. We also now offer single collection versions of our SMRT Cell 8M and Sequencing kit and consumables, offering users the flexibility to run small, single SMRT Cell runs when convenient.
Learn how these consumables can elevate your whole genome sequencing, variant detection, epigenome analysis, and full-length RNA sequencing research with quick turnaround times to characterize SNVs, structural variants, splice isoforms, and improved genome annotation with high accuracy.