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STRN50

Spectrum Plant Total RNA Kit

greener alternative

sufficient for 50 purifications

Synonym(s):

Plant total RNA extraction kit, Plant total RNA isolation kit, Plant total RNA purification kit

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Pack SizeSKUAvailabilityPrice
1 kit

Estimated to ship onJune 18, 2026fromMILWAUKEE

$392.00

About This Item

NACRES:
NA.52
UNSPSC Code:
41105501

$392.00


Estimated to ship onJune 18, 2026Details


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usage

sufficient for 50 purifications

Quality Level

greener alternative product characteristics

Designing Safer Chemicals
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

technique(s)

RNA purification: suitable

test parameters

: ~30 min kit run time, sample volume: 100 mg

greener alternative category

storage temp.

15-25°C

General description

The Spectrum Plant Total RNA Kit utilizes a lysis and binding chemistry and a convenient column-based ′bind-wash-and-elute′ format to purify up to 100 μg of total RNA from 100 mg of tissue in about 30 minutes. Typical yields range from 20–60 μg.

After grinding tissue to a fine powder in liquid nitrogen, cells are lysed and cellular debris is physically and chemically separated from endogenous RNA. RNA is then bound to a column supported silica substrate and several wash steps remove remaining contaminants.

Total RNA is eluted from the column and used in typical applications, such as Northern Blots, and RT- and qRT-PCR.
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has Inherently Safer Chemistry.

Application

Spectrum Plant Total RNA Kit has been used to isolate RNA from ground fiber tissue of cultured cotton fiber, from neem tissues and from Sarracenia, an insectivorous plant.[1]

Features and Benefits

  • Yields up to 60 μg of pure concentrated RNA per prep
  • Efficient protocol allows for RNA purification in 30 min or less
  • Specially designed for research with difficult plant tissues

Legal Information

Spectrum is a trademark of Sigma-Aldrich Co. LLC

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STRN250STRN10RTN350
usage

sufficient for 50 purifications

usage

sufficient for 250 purifications

usage

sufficient for 10 purifications

usage

sufficient for 350 purifications

technique(s)

RNA purification: suitable

technique(s)

RNA purification: suitable

technique(s)

RNA purification: suitable

technique(s)

RNA purification: suitable

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

greener alternative product characteristics

Designing Safer Chemicals
Learn more about the Principles of Green Chemistry.

greener alternative product characteristics

Designing Safer Chemicals
Learn more about the Principles of Green Chemistry.

greener alternative product characteristics

Designing Safer Chemicals
Learn more about the Principles of Green Chemistry.

greener alternative product characteristics

Designing Safer Chemicals
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

sustainability

Greener Alternative Product

sustainability

Greener Alternative Product

sustainability

Greener Alternative Product

greener alternative category

Aligned,

greener alternative category

Aligned,

greener alternative category

, Aligned

greener alternative category

Aligned,


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Kit Components Only

Product No.
Description

  • Binding Solution

  • Lysis Solution

  • Wash Solution 1

Kit Components Also Available Separately

Product No.
Description
SDS & Pricing

  • 2-Mercaptoethanol, Molecular Biology, suitable for electrophoresis, suitable for cell culture, BioReagent, 99% (GC/titration)
    SDS

signalword

Danger

Hazard Classifications

Acute Tox. 2 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Eye Dam. 1 - Repr. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT RE 2 Oral

target_organs

Liver,Heart

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3



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Articles

Simple DNA/RNA purification methods aid genome analysis from various sources, enhancing research efficiency.

Related Content

The Spectrum Plant Total RNA Kit incorporates a new, patent-pending lysis and binding chemistry. This kit is intended to purify total RNA from species and tissue where most Total RNA protocols fail. Without sacrificing affordability, you can purify more total RNA per isolation.


Jinbu Jia et al.
The Plant cell, 32(12), 3662-3673 (2020-10-21)
In plants, 22-nucleotide small RNAs trigger the production of secondary small interfering RNAs (siRNAs) and enhance silencing. DICER-LIKE2 (DCL2)-dependent 22-nucleotide siRNAs are rare in Arabidopsis (Arabidopsis thaliana) and are thought to function mainly during viral infection; by contrast, these siRNAs
Asfaw Degu et al.
BMC plant biology, 19(1), 69-69 (2019-02-13)
Grape leaves provide the biochemical substrates for berry development. Thus, understanding the regulation of grapevine leaf metabolism can aid in discerning processes fundamental to fruit development and berry quality. Here, the temporal alterations in leaf metabolism in Merlot grapevine grown
A synthetic auxin (NAA) suppresses secondary wall cellulose synthesis and enhances elongation in cultured cotton fiber.
Singh B
Plant Cell Reports, 28(7), 1023-1032 (2009)



Global Trade Item Number

SKUGTIN
STRN50-1KT04061835575008

Questions

1–3 of 3 Questions  
  1. What composition of your elution buffer (E8024-50ml) in plant total RNA kit?

    1 answer
    1. The composition of this product is considered proprietary.

      Helpful?

  2. Is it suitable for use with chestnut samples?

    Is it suitable for use with chestnut samples?

    1 answer
    1. The kit has been utilized for chestnut samples, as reported in the following paper: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4615883/

      Helpful?

  3. We need to know the elution buffer composition for downstream quantification and sequencing. What solution can be used besides the original elution buffer that can have the same proprerties to be used as a blank?

    1 answer
    1. A suitable solution would be molecular biology-grade water or nuclease-free water. These types of water are typically free of contaminants and nucleases, making them ideal for use as a blank solution in downstream quantification and sequencing experiments.

      Helpful?

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