Protocol: A simple phenol-based method for 96-well extraction of high quality RNA from Arabidopsis
<p>Abstract</p> <p>Background</p> <p>Many experiments in modern plant molecular biology require the processing of large numbers of samples for a variety of applications from mutant screens to the analysis of natural variants. A severe bottleneck to many such analyses is...
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doaj-8bc3f9e6526641238379f344e1fa70a42020-11-24T23:46:18ZengBMCPlant Methods1746-48112011-03-0171710.1186/1746-4811-7-7Protocol: A simple phenol-based method for 96-well extraction of high quality RNA from ArabidopsisCoustham VincentBox Mathew SDean CarolineMylne Joshua S<p>Abstract</p> <p>Background</p> <p>Many experiments in modern plant molecular biology require the processing of large numbers of samples for a variety of applications from mutant screens to the analysis of natural variants. A severe bottleneck to many such analyses is the acquisition of good yields of high quality RNA suitable for use in sensitive downstream applications such as real time quantitative reverse-transcription-polymerase chain reaction (real time qRT-PCR). Although several commercial kits are available for high-throughput RNA extraction in 96-well format, only one non-kit method has been described in the literature using the commercial reagent TRIZOL.</p> <p>Results</p> <p>We describe an unusual phenomenon when using TRIZOL reagent with young Arabidopsis seedlings. This prompted us to develop a high-throughput RNA extraction protocol (HTP96) adapted from a well established phenol:chloroform-LiCl method (P:C-L) that is cheap, reliable and requires no specialist equipment. With this protocol 192 high quality RNA samples can be prepared in 96-well format in three hours (less than 1 minute per sample) with less than 1% loss of samples. We demonstrate that the RNA derived from this protocol is of high quality and suitable for use in real time qRT-PCR assays.</p> <p>Conclusion</p> <p>The development of the HTP96 protocol has vastly increased our sample throughput, allowing us to fully exploit the large sample capacity of modern real time qRT-PCR thermocyclers, now commonplace in many labs, and develop an effective high-throughput gene expression platform. We propose that the HTP96 protocol will significantly benefit any plant scientist with the task of obtaining hundreds of high quality RNA extractions.</p> http://www.plantmethods.com/content/7/1/7 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Coustham Vincent Box Mathew S Dean Caroline Mylne Joshua S |
spellingShingle |
Coustham Vincent Box Mathew S Dean Caroline Mylne Joshua S Protocol: A simple phenol-based method for 96-well extraction of high quality RNA from Arabidopsis Plant Methods |
author_facet |
Coustham Vincent Box Mathew S Dean Caroline Mylne Joshua S |
author_sort |
Coustham Vincent |
title |
Protocol: A simple phenol-based method for 96-well extraction of high quality RNA from Arabidopsis |
title_short |
Protocol: A simple phenol-based method for 96-well extraction of high quality RNA from Arabidopsis |
title_full |
Protocol: A simple phenol-based method for 96-well extraction of high quality RNA from Arabidopsis |
title_fullStr |
Protocol: A simple phenol-based method for 96-well extraction of high quality RNA from Arabidopsis |
title_full_unstemmed |
Protocol: A simple phenol-based method for 96-well extraction of high quality RNA from Arabidopsis |
title_sort |
protocol: a simple phenol-based method for 96-well extraction of high quality rna from arabidopsis |
publisher |
BMC |
series |
Plant Methods |
issn |
1746-4811 |
publishDate |
2011-03-01 |
description |
<p>Abstract</p> <p>Background</p> <p>Many experiments in modern plant molecular biology require the processing of large numbers of samples for a variety of applications from mutant screens to the analysis of natural variants. A severe bottleneck to many such analyses is the acquisition of good yields of high quality RNA suitable for use in sensitive downstream applications such as real time quantitative reverse-transcription-polymerase chain reaction (real time qRT-PCR). Although several commercial kits are available for high-throughput RNA extraction in 96-well format, only one non-kit method has been described in the literature using the commercial reagent TRIZOL.</p> <p>Results</p> <p>We describe an unusual phenomenon when using TRIZOL reagent with young Arabidopsis seedlings. This prompted us to develop a high-throughput RNA extraction protocol (HTP96) adapted from a well established phenol:chloroform-LiCl method (P:C-L) that is cheap, reliable and requires no specialist equipment. With this protocol 192 high quality RNA samples can be prepared in 96-well format in three hours (less than 1 minute per sample) with less than 1% loss of samples. We demonstrate that the RNA derived from this protocol is of high quality and suitable for use in real time qRT-PCR assays.</p> <p>Conclusion</p> <p>The development of the HTP96 protocol has vastly increased our sample throughput, allowing us to fully exploit the large sample capacity of modern real time qRT-PCR thermocyclers, now commonplace in many labs, and develop an effective high-throughput gene expression platform. We propose that the HTP96 protocol will significantly benefit any plant scientist with the task of obtaining hundreds of high quality RNA extractions.</p> |
url |
http://www.plantmethods.com/content/7/1/7 |
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