Literature DB >> 32633638

Comparison of commercial manual extraction kits for RNA isolation from canine whole blood.

Dahlia H Tesfamichael1, Michael W Wood1, Jessica C Pritchard1.   

Abstract

High quantities of quality RNA are necessary for many veterinary laboratory tests. Several commercial kits are available for RNA isolation from human whole blood; their resultant RNA yield and purity have not been reported for canine whole blood, to our knowledge. We assessed the performance of 4 RNA extraction kits (RiboPure, TRIzol, RNeasy Protect animal blood, and QIAamp RNA blood mini). Whole blood from a healthy dog was stored in the manufacturer-recommended RNA stabilizing buffer as directed. RNA isolation, including DNase treatment, was performed using each kit's manufacturer's protocol. Resultant RNA yield and purity were evaluated using spectrophotometric absorbance, capillary electrophoresis and electropherogram analysis, and a reverse-transcription real-time PCR (RT-rtPCR) assay. The RNeasy Protect animal blood kit extracted the highest, and RiboPure the lowest, concentration of nucleic acid. RNA integrity numbers classified extracted RNA as good quality or better for all kits except RNeasy Protect. All kits had evidence of genomic DNA contamination as assessed by RT-rtPCR. Overall, QIAamp RNA blood mini kit and TRIzol optimized both RNA yield and purity from canine whole blood. These kits extracted high quantities of good quality RNA as evidenced by high RNA integrity numbers and minimal contamination with proteins and solvents.

Entities:  

Keywords:  DNA contamination; PCR; RNA extraction; RNA stability; dogs; genomics

Mesh:

Substances:

Year:  2020        PMID: 32633638      PMCID: PMC7488962          DOI: 10.1177/1040638720938026

Source DB:  PubMed          Journal:  J Vet Diagn Invest        ISSN: 1040-6387            Impact factor:   1.279


  8 in total

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Journal:  Int J Biol Markers       Date:  2012-07-19       Impact factor: 2.659

2.  Evaluation of a low-cost procedure for sampling, long-term storage, and extraction of RNA from blood for qPCR analyses.

Authors:  Rasmus B Mærkedahl; Hanne Frøkiær; Lotte Lauritzen; Stine B Metzdorff
Journal:  Clin Chem Lab Med       Date:  2015-07       Impact factor: 3.694

3.  Identification and characterization of immunoglobulin G in blood as a major inhibitor of diagnostic PCR.

Authors:  W A Al-Soud; L J Jönsson; P Râdström
Journal:  J Clin Microbiol       Date:  2000-01       Impact factor: 5.948

4.  Identification of the heme compound copurified with deoxyribonucleic acid (DNA) from bloodstains, a major inhibitor of polymerase chain reaction (PCR) amplification.

Authors:  A Akane; K Matsubara; H Nakamura; S Takahashi; K Kimura
Journal:  J Forensic Sci       Date:  1994-03       Impact factor: 1.832

5.  Comparison of methods for improved RNA extraction from blood for early detection of Classical swine fever virus by real-time reverse transcription polymerase chain reaction.

Authors:  Amaresh Das; Tammy R Beckham; Michael T McIntosh
Journal:  J Vet Diagn Invest       Date:  2011-06-08       Impact factor: 1.279

6.  Efficient recovery of whole blood RNA--a comparison of commercial RNA extraction protocols for high-throughput applications in wildlife species.

Authors:  Doreen Schwochow; Laurel E K Serieys; Robert K Wayne; Olaf Thalmann
Journal:  BMC Biotechnol       Date:  2012-06-27       Impact factor: 2.563

7.  Gene expression profiling of whole blood: A comparative assessment of RNA-stabilizing collection methods.

Authors:  Duncan E Donohue; Aarti Gautam; Stacy-Ann Miller; Seshamalini Srinivasan; Duna Abu-Amara; Ross Campbell; Charles R Marmar; Rasha Hammamieh; Marti Jett
Journal:  PLoS One       Date:  2019-10-10       Impact factor: 3.240

8.  Isolation of RNA from equine peripheral blood cells: comparison of methods.

Authors:  Zibin Jiang; Cornelius E Uboh; Jinwen Chen; Lawrence R Soma
Journal:  Springerplus       Date:  2013-09-22
  8 in total

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