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BioQule Bleed to Read DNA Library Prep Kit

The BioQule Bleed to Read DNA Library Prep Kit enables the preparation of up to 8 uniquely dual-indexed paired-end DNA libraries directly from human whole blood using the BioQule NGS System. Streamline your genomic research workflow with minimal hands-on time and ensure robust performance for Illumina® sequencing platforms.

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Feature Specification
Application DNA isolation
DNA-seq library prep
Automation Compatible Yes
Instrument Compatibility Bioqule NGS System
Sample Type Blood
Type DNA Seq
Technology Capillary Liquid Handling

The BioQule Bleed to Read DNA Library Prep Kit enables the preparation of up to 8 uniquely dual-indexed paired-end DNA libraries directly from human whole blood using the BioQule NGS System. Streamline your genomic research workflow with minimal hands-on time and ensure robust performance for Illumina® sequencing platforms.

Click to copy promo code to clipboard.
img-icon-10-off-white-yellow.svg

SAVE 10% on your first Revvity.com order. Use promo code below.

HELLO10

Terms and conditions apply.

Product Variant
Unit Size: 8 rxns
Part #:
900-000021
List Price
USD 462.00
Your online price:
For research use only. Not for use in diagnostic procedures.

Overview

Designed for the automated preparation of DNA libraries directly from human whole blood, the BioQule™ Bleed to Read DNA Library Prep Kit offers an efficient and reliable solution for genomic research. This kit allows the creation of up to 8 uniquely dual-indexed paired-end double-stranded DNA libraries with reduced hands-on time by up to 80%. Compatible with Illumina sequencing platforms, it ensures robust results with robust genome coverage and minimized sequencing bias. The kit includes all necessary reagents and components, simplifying the workflow and enhancing laboratory efficiency. Ideal for applications such as whole-genome sequencing and targeted sequencing, the BioQule™ Bleed to Read DNA Library Prep Kit provides a comprehensive solution for your NGS needs.

Please note that barcodes and a BioQule NGS Cartridge (P/N CLS158240) must be purchased separately.

Key Features:

  • Sample Source: Human whole blood with sodium citrate or EDTA anticoagulants.
  • High Throughput: Prepare up to 8 DNA libraries in a single run.
  • Automated Workflow: Reduces hands-on time by up to 80%, enhancing lab efficiency.
  • Sequencing Compatibility: Functionally tested for Illumina® sequencing platforms.
  • Robust Performance: Ensures results with minimized sequencing bias

Kit Contents

  • BioQule™ Bleed to Read™ DNA Library Reagent Kit
  • BioQule DNA Clean Up Beads
  • BioQule Extraction Beads
  • BioQule Lysis Buffer
  • BioQule Fragmentation Enzyme
  • BioQule Fragmentation Buffer
  • BioQule Resuspension Buffer
  • BioQule Optics Standard

Specifications

Application
DNA isolation
DNA-seq library prep
Automation Compatible
Yes
Hands on Time
15 minutes
Instrument Compatibility
Bioqule NGS System
Sample Type
Blood
Shipping Conditions
Shipped in Dry Ice
Technology
Capillary Liquid Handling
Type
DNA Seq
Unit Size
8 rxns

Resources

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Application Note
Bleed to read - from blood samples to ready-to-use NGS libraries

Next-Generation Sequencing (NGS) is becoming readily accessible; however, nucleic acid purification and library preparation are...

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