MRN10
GenElute™ mRNA Miniprep Kit
sufficient for 10 purifications
Synonym(s):
GenElute™ mRNA Kit, Gen Elute
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About This Item
NACRES:
NA.52
UNSPSC Code:
41105501
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usage
sufficient for 10 purifications
Quality Level
technique(s)
RNA purification: suitable
input
mammalian cells
mammalian tissue
RNA (total)
test parameters
: <40 min kit run time, sample volume: 250 μL with up to 500 µg total RNA
storage temp.
15-25°C
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Related Categories
1 of 4
This Item | |||
|---|---|---|---|
| technique(s) RNA purification: suitable | technique(s) RNA purification: suitable | technique(s) RNA purification: suitable | technique(s) - |
| usage sufficient for 10 purifications | usage sufficient for 70 purifications | usage sufficient for 10 purifications | usage sufficient for 70 purifications |
MRN70 | MRN10 | DMN70 | DMN10 |
| storage temp. 15-25°C | storage temp. 15-25°C | storage temp. 15-25°C | storage temp. 15-25°C |
| Quality Level 200 | Quality Level 200 | Quality Level 200 | Quality Level 200 |
General description
Procedures such as cDNA synthesis, expression profiling and others require separation of mRNA from the vastly more abundant rRNA and tRNA. The GenElute mRNA kits provide convenient procedures for isolating polyadenylated mRNA from previously prepared total RNA or directly from mammalian cells and tissues. For direct mRNA preparation, cells or tissues are disrupted with SDS/proteinase K digestion to release RNA and eliminate RNases. Both kit types use oligo dT30 covalently linked to 1 μm polystyrene beads to capture polyadenylated mRNA by hybridization. The polystyrene beads remain suspended during hybridization, eliminating the need for mixing or rocking, as is common for cellulose or magnetic particles. Polystyrene was also chosen because oligo(dT) polystyrene beads yield cleaner mRNA with fewer stringent washing steps than does the more commonly used oligo(dT) cellulose (2 or 3 wash steps versus 10 or more). With the GenElute kits, mRNA-bead complexes are washed on a microcentrifuge spin filter, and eluted into 10 mM Tris-HCL, pH 7.5. mRNA prepared with either kit is suitable for a variety of downstream applications such as Northern blotting, expression array or chip hybridizations and cDNA synthesis and library construction.
The GenElute mRNA Miniprep Kit provides a simple and convenient way to purify polyadenylated mRNA from previously isolated total RNA. Oligo(dT) polystyrene beads bind the poly(A)+ mRNA during a 10 minute incubation. After washing in a microspin filter to remove contaminants, the poly(A)+ mRNA is eluted in 100 mL of buffer. Purification of mRNA from total RNA, can be performed in less than 40 minutes.
The purified mRNA is ready for Northern analysis, reverse transcription and PCR, labeling for arrays, and other common applications.
The purified mRNA is ready for Northern analysis, reverse transcription and PCR, labeling for arrays, and other common applications.
Application
The purified mRNA is ready for Northern analysis, reverse transcription and PCR, labeling for arrays, and other common applications.
Features and Benefits
- Quick and convenient reagent for use in the simultaneous isolation of RNA, DNA and protein
- Performs well with large or small amounts of tissue or cells and many samples can be simultaneously extracted
- One of the most effective methods for isolating total RNA. Purifications can be completed in only one hour starting with fresh tissue or cells
- mRNA captured on oligo(dT) polystyrene beads in 10 minutes
- Oligo(dT) polystyrene beads require fewer wash steps
- Poly (A)+ mRNA isolated from previously purified total RNA in 40 minutes
Other Notes
For additional information, please see www.sigma-aldrich.com/mrna.
Legal Information
GenElute is a trademark of Sigma-Aldrich Co. LLC
Kit Components Only
Product No.
Description
- 2X Binding solution
- Wash Solution
Kit Components Also Available Separately
Product No.
Description
SDS
- W4502Water, Nuclease-Free Water, for Molecular Biology
Storage Class
10 - Combustible liquids
wgk
WGK 3
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Host translation is generally modulated by viral infection, including duck hepatitis A virus (DHAV) infection. Previously, we reported that cellular protein synthesis in a cell model of duck embryo fibroblasts is significantly inhibited by DHAV infection but not viral proteins
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G3 (Bethesda, Md.), 9(8), 2511-2520 (2019-06-27)
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Diabetic nephropathy (DN) is prevalent in patients with diabetes. N6-methyladenosine (m6A) methylation has been found to cause modification of nucleotide-binding oligomerization domain, leucine-rich repeat, and pyrin domain-containing (NLRP) 3, which is involved in cell pyroptosis and inflammation. WTAP is a
Global Trade Item Number
| SKU | GTIN |
|---|---|
| MRN10-1KT | 04061834066859 |
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