Evidence map›Paper›PMID 21443767›Full record

ArticleBMC research notes2011

An RNA isolation system for plant tissues rich in secondary metabolites.

Sanjay Ghawana, Asosii Paul, Hitesh Kumar, Arun Kumar, Harsharan Singh, Pardeep K Bhardwaj, Arti Rani, Ravi S Singh, Jyoti Raizada, Kashmir Singh and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMC research notes, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 125 papers.

0numbers the graph read from it
0cells of the map it votes in
125citing papers in PubMed
5.5field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

125 citing papers in PubMed, 309 citations in OpenAlex.

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65 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

11 authors at 4 institutions in 1 country.

Sanjay GhawanaBiotechnology Division, Institute of Himalayan Bioresource Technology (CSIR), Palampur-176 061, Himachal Pradesh, India. sanjayplp1@gmail.com.
Asosii Paul
Hitesh Kumar
Arun Kumar
Harsharan Singh
Pardeep K Bhardwaj
Arti Rani
Ravi S Singh
Jyoti Raizada
Kashmir Singh
Sanjay Kumar
Institute of Himalayan Bioresource Technology · INChaudhary Sarwan Kumar Himachal Pradesh Krishi Vishvavidyalaya · INPanjab University · INPunjab Technical University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSecondary metabolites are reported to interfere with the isolation of RNA particularly with the recipes that use guanidinium-based salt. Such interference was observed in isolation of RNA with medicinal plants rheum (Rheum australe) and arnebia (Arnebia euchroma). A rapid and less cumbersome system for isolation of RNA was essential to facilitate any study related to gene expression.

findingsAn RNA isolation system free of guanidinium salt was developed that successfully isolated RNA from rheum and arnebia. The method took about 45 min and was successfully evaluated on twenty one tissues with varied secondary metabolites. The A260/280 ratio ranged between 1.8 - 2.0 with distinct 28 S and 18 S rRNA bands visible on a formaldehyde-agarose gel.

conclusionsThe present manuscript describes a rapid protocol for isolation of RNA, which works well with all the tissues examined so far. The remarkable feature was the success in isolation of RNA with those tissues, wherein the most commonly used methods failed. Isolated RNA was amenable to downstream applications such as reverse transcription-polymerase chain reaction (RT-PCR), differential display (DD), suppression subtractive hybridization (SSH) library construction, and northern hybridization.

Identifiers

PMID21443767
PMCPMC3079660
OpenAlexW2084244231

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.