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Sigma-Aldrich

GenElute Mammalian Total RNA Miniprep Kit

greener alternative

sufficient for 70 purifications

Synonym(s):

GenElute Mammalian RNA Kit, animal total RNA purification kit, cell RNA extraction kit, cell RNA isolation kit, cell total RNA purification kit, tissue total RNA purification kit, total RNA extraction kit, total RNA isolation kit, total RNA purification kit, Gen Elute

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About This Item

UNSPSC Code:
41105501
NACRES:
NA.52

usage

sufficient for 70 purifications

greener alternative product characteristics

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

sustainability

Greener Alternative Product

technique(s)

RNA purification: suitable

greener alternative category

storage temp.

15-25°C

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General description

Sigma′s GenElute Mammalian Total RNA Miniprep Kit provides a simple and convenient way to isolate total RNA from mammalian cells and tissues. Protocols are provided for cells, tissues, and fibrous tissues. These protocols differ in their cell lysis and disruption conditions. Once the RNA is bound to the GenElute Binding Column, the purification procedure is the same for all starting materials. For fibrous tissues the kit must be used with proteinase K (Cat. No. P4850) to ensure effective cell disruption. The kit combines the advantages of a silica-based system with a microspin format and eliminates the need for cesium chloride gradients, alcohol precipitation, and hazardous organic compounds such as phenol and chloroform. Cells or tissues are lysed and homogenized in a buffer containing guanidine thiocyanate to ensure thorough
denaturation of macromolecules and inactivation of RNases. Addition of ethanol causes RNA to bind when the lysate is spun through a silica membrane in a microcentrifuge tube. After washing to remove contaminants, RNA is eluted in 50-100 μL of Elution Solution. Up to 150 μg of total RNA can be isolated in less than 30 minutes.

If all traces of DNA contamination must be eliminated, further treatment with DNase I is recommended. DNase I digestion can be performed while the RNA is bound to the GenElute Binding Column using the On-Column DNase I Digestion Set (DNASE10 and DNASE70). Alternatively, for more stringent removal of contaminating DNA, the final RNA preparation can be treated with Amplification Grade DNase I (AMPD1).
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, compared to the standard use of phenol and chloroform to perform DNA extractions.

Application

GenElute Mammalian Total RNA Miniprep Kit has been used to isolate total RNA:
  • from snap-frozen preoptic area of rat brain
  • from central part of the mantle tissue containing gonads of Mytilus trossulus mussel
  • from murine liver
The purified RNA is ready for reverse transcription and PCR, labeling and microarray analysis, and other common applications. Note that RNA shorter than 200 nucleotides in length, such as tRNA, 5S rRNA, and 5.8S rRNA, is not recovered efficiently under the conditions used with this kit.

Features and Benefits

  • Purifies total RNA from up to 107 cells or 40 mg of tissue per prep
  • Yields up to 150 μg of pure, concentrated total RNA per prep
  • Recover RNA from as few as 100 cells
  • Simple and efficient–12 to 18 preps in 30 minutes
  • Faster than gravity flow anion exchange methods
  • No cumbersome steps associated with resins and magnetic slurries
  • 40% more purifications per kit than the leading supplier

Other Notes

The GenElute Mammalian Total RNA Purification Kit combines silica-membrane technology with a convenient spin column format for a rapid bind, wash, and elute method to prepare high quality total RNA.
For additional information, please see www.sigma-aldrich.com/totalrna.

Principle

Samples are lysed and homogenized in guanidine thiocyanate and 2-mercaptoethanol to release RNA and inactivate RNases. Lysates are spun through a filtration column to remove cellular debris and shear DNA. The filtrate is then applied to a high capacity silica column to bind total RNA, followed by washing and elution. Up to 150 μg of total RNA can be recovered per prep in 100 μl of water. The purified RNA is ready for Northern blots (Fig. 1), RT-PCR (Fig. 2) and other common applications.

Legal Information

GenElute is a trademark of Sigma-Aldrich Co. LLC

Signal Word

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 Corr. 1C - Skin Sens. 1 - STOT RE 2 Oral

Target Organs

Liver,Heart

Supplementary Hazards

Storage Class Code

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


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Co-expressed mitochondrial genomes: recently masculinized, recombinant mitochondrial genome is co-expressed with the female-transmitted mtDNA genome in a male Mytilus trossulus mussel from the Baltic Sea.
Sanko TJ and Burzynski A
BMC Genetics, 15, 28-28 (2014)
Sex differences in epigenetic regulation of the estrogen receptor-alpha promoter within the developing preoptic area.
Kurian JR
Endocrinology, 151(5), 2297-2305 (2010)
Resveratrol exerts a biphasic effect on apolipoprotein M.
Kurano M
British Journal of Pharmacology, 173(1), 222-233 (2016)
Sho Hasegawa et al.
Kidney international, 97(5), 934-950 (2020-03-17)
Hypoxia-inducible factor (HIF) prolyl hydroxylase inhibitors, also known as HIF stabilizers, increase endogenous erythropoietin production and serve as novel therapeutic agents against anemia in chronic kidney disease. HIF induces the expression of various genes related to energy metabolism as an
Jessica L Teo et al.
Developmental cell, 54(1), 75-91 (2020-06-03)
Epithelia are active materials where mechanical tension governs morphogenesis and homeostasis. But how that tension is regulated remains incompletely understood. We now report that caveolae control epithelial tension and show that this is necessary for oncogene-transfected cells to be eliminated

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