Isolation and Separation of DNA and RNA from a Single Tissue or Cell Culture Sample

Content Type: Poster
Authors: Han Wei Ph.D.; Lauren Saunders Ph.D.; Brittany Niccum Ph.D.; Antonia Hur; Asmita Patel

Introduction

Understanding the transcriptome and the genome of any organism relies on the accurate sequencing of both the RNA and DNA from an organism.

Current technologies rely on splitting a sample pool in two after or before lysis. This in effect only allows for half of the total RNA or DNA available to be isolated and requires either a large sample size or two separate sample pools.

To overcome this challenge, we are currently developing a product using proprietary bead based technology that selectively binds DNA to the beads to effectively separate DNA and RNA independently. This allows for the extraction of all nucleic acids from one experimental setup.

Versatile Workflow for a Variety of Sample Types

Genomics Poster Workflow for Variety of Sample Types

  • Extraction has been demonstrated with tissue and cell samples
  • Extraction is being optimized for additional sample types
  • Our team of Proof of Principle scientists can help you adapt this workflow to your sample type

AMPure XP as a Tool for Nucleic Acid Extraction

Beckman Coulter Life Sciences Offers a Variety of Extraction Kits based on the same technology as AMPure XP. These chemistries are customizable for you DNA and RNA extraction needs.Genomics Poster Variety of Extraction Kits

  • Beads don’t clog like columns can with viscous samples
  • Gentler on nucleic acid since does not have to be pulled through columns
  • Workflows are straightforward and can be adapted for many different sample types

Tissue Sample

Genomics Poster Tissue YieldDNA and RNA was isolated from 10mg of mouse liver tissue by using selective binding of DNA. The yield of nucleic acid was estimated using the Quant-iT DNA assay kit (Thermo Fisher Scientific). The size of DNA and RNA was visualized on the Agilent Genomic DNA Screen Tape and RNA Screen Tap.

  • DNA yield averaged 32 μg, RNA yield averaged 66 μg from three technical replicates
  • DNA sizes averaged >60,000 bp, and two prominent rRNA peaks were observed in the RNA fraction

Genomics Poster DNA Tissue

Genomics Poster RNA Tissue

Cell Culture Sample

Genomics Poster Cell Culture SampleDNA and RNA was isolated from increasing amounts of cells.

  • Both DNA and RNA yield increased linearly with cell input
  • The DIN and RIN scores for DNA and RNA isolated from 50,000, 100,000 and 500,000 cells were consistent and above 9; indicating that DNA and RNA is intact
  • The concentration of nucleic acids from 10,000 was too low for an accurate measurement

Genomics Poster DNA Traces Cell Culture Sample

Genomics Poster RNA Traces Cell Culture Sample

Cell Number DIN Score (DNA Integrity) RIN Score (RNA Integrity)
50,000 9.2 9.5
100,000 9.0 9.2
500,000 9.1 9.4

 

 

Beckman Coulter makes no warranties of any kind whatsoever express or implied, with respect to these protocols, including but not limited to warranties of fitness for a particular purpose or merchantability or that the protocol is non-infringing. All warranties are expressly disclaimed. Your use of the method is solely at your own risk, without recourse to Beckman Coulter. Not intended or validated for use in the diagnosis of disease or other conditions. These protocols are for demonstration only, and are not validated by Beckman Coulter. © 2019 Beckman Coulter, Inc. All rights reserved. Beckman Coulter, the stylized logo, and the Beckman Coulter product and service marks mentioned herein are trademarks or registered trademarks of Beckman Coulter, Inc. in the United States and other countries. All other trademarks are the property of their respective owners.

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