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Next Generation Sequencing

Tools to Streamline Your NGS Workflow

Next Generation Sequencing

Tools to Streamline Your NGS Workflow


Next generation sequencing (NGS) is a method of high-throughput sequencing in which millions of DNA strands can be sequenced in parallel. Many researchers use NGS as an important tool to gain insight into the detailed and comprehensive genetic and epigenetic modifications of genomes from many different cell types. Choose from our comprehensive mix of kits to extract and prepare your library sample for NGS analysis.

Whether you are preparing samples for ChIP-seq, whole genome sequencing, or Bisuilfite-sequencing our kits are easy, efficient, and convenient.


Reliable and Streamlined NGS Workflow


Nucleic Acid Extraction


  • Fast – Entire procedure can be finished in as little as 15 minutes with consistent isolation conditions
  • Effective – High efficiency of nucleic acid isolation from various sample types with low amounts of start material (as low as 1 ng)
  • Reliable – Our specially designed columns allow for nucleic acids to be conveniently recovered
  • Safe – Use of non-toxic reagents and no phenol chloroform


Product Name Sample Input Elution Volume Protocol Time
AMPIXTRACT™ General Tissue Section DNA Isolation Kit 1 ng (optimal range 10 ng – 1 μg) 8 - 20 μL 2 hours
AMPIXTRACT™ Paraffin Tissue Section DNA Isolation Kit 1 ng (optimal range 10 ng – 1 μg) 8 - 20 μL 2 hours
AMPIXTRACT™ Urine DNA Isolation Kit 1 ng – 2 μg (optimal range 10 ng – 1 μg) 8 - 20 μL 20 minutes
AMPIXTRACT™ Blood and Cultured Cell DNA Extraction Kit 1 ng – 4 μg (optimal range 10 ng – 1 μg) 10 - 20 μL 20 minutes
EPIXTRACT® DNA Isolation Kit for Plasma/Serum 0.1 ng (optimal range 1 ng – 1 μg) 8 - 20 μL 15 minutes

Library Preparation



  • Fast and Streamlined Procedure – Compact protocols with simple clean-up steps to save time and prevent handling errors, as well as loss of valuable samples
  • Highly Convenient – The kit contains all required components for each step of the library preparation for the most reliable and consistent results
  • Minimize bias – High quality enzymes achieve reproducibly high yields of nucleic acid library with minimal sequence bias and low error rates
  • Flexibility – Can be used for both non-barcoded (singleplexed) and barcoded (multiplexed) library preparation with broad range of nucleic acid input


Product Name DNA Bisulfite-Seq Post Bisulfite-Seq ChIP-Seq
AMPINEXT™ DNA Library Preparation Kit AMPINEXT™ High-Sensitivity DNA Library Preparation Kit AMPINEXT™ High-Sensitivity Bisulfite-Seq Kit AMPINEXT™ RNA Bisulfite-Seq Kit AMPINEXT™ 5-mC RNA Bisulfite-Seq Easy Kit AMPINEXT™ Post-Bisulfite DNA Library Preparation Kit AMPINEXT™ ChIP-Seq High-Sensitivity Kit
Input Type DNA DNA DNA RNA RNA DNA Cells Tissues
Input Range 5 ng – 1 μg 0.2 ng – 100 ng 0.2 ng – 200 ng 5 ng – 1 μg 5 ng – 500 ng 0.5 ng – 1 μg 105 – 106 Cells 5 mg – 50 mg
(Optimal Range) (100 ng – 200 ng) (10 ng – 50 ng) (10 ng – 50 ng) (200 ng – 500 ng) (100 ng – 200 ng) (100 ng – 200 ng) (4×105 – 5×105 Cells) 20 mg – 30 mg)
Protocol Time < 2.5 hours < 1.5 hours < 6.5 hours 6 hours 5 hours < 7 hours

Related Products


Product Name Contents
AMPINEXT™ DNA Size Selection Kit MQ Binding Beads, Elution Solution, 96-well plate
AMPINEXT™ NGS Barcode (Index) Set-12 AMPINEXT™ Barcodes 1-12 (10 μM)
AMPINEXT™ Universal Primer (10 μM)

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