As per the product information sheet, 100% Ethanol is suggested for the dilution of the wash solution. The use of 100% methanol has not been validated and is not recommended for the isolation of RNA. Kindly review the product information sheet available at this link: https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/product/documents/188/017/snc10bul.pdf
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A propos de cet article
General description
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Application
- extract total RNA containing miRNA from grape edible plant derived exosome-like nanoparticles (EPDEN).
- isolate small RNA from S.sirkka and S. napiecek, and S. arctica.[1]
- extract miRNA, from frozen rat livers for miRNA analysis.
Features and Benefits
- Designed to enhance the efficiency of isolating microRNA and other small RNA molecules directly from a wide range of biological sources.
- Enables fast and efficient extraction and concentration of miRNA in 30 minutes for downstream applications.
- Can extract high-purity miRNA with no detectable large RNA
- No dangerous organic extractions are involved.
Legal Information
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Cet article | |||
|---|---|---|---|
| technique(s) DNA extraction: suitable | technique(s) DNA extraction: suitable | technique(s) RNA purification: suitable | technique(s) RNA purification: suitable |
| usage sufficient for 50 preparations | usage sufficient for 10 preparations | usage sufficient for 350 purifications | usage sufficient for 70 purifications |
| Quality Level 200 | Quality Level 200 | Quality Level 200 | Quality Level 200 |
SNC10 | SNC50 | RTN10, RTN70, RTN9602, RTN9604 | RTN10, RTN350, RTN9602, RTN9604 |
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Composants de kit seuls
- Binding Solution 2
- Lysis Solution
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2
Classe de stockage
10 - Combustible liquids
flash_point_f
Not applicable
flash_point_c
Not applicable
wgk
WGK 3
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Methanol 100% can be used for the dilution of the wash solution instead of ethanol 100%?
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How can I avoid co-purifying mRNAs and rRNAs when purifying small RNAs from gram negative bacteria using mirPremier® microRNA Isolation Kit?
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Too much residual medium or cell mass may lead to recovery of some large RNAs. It is critical to remove as much residual medium as possible by re-centrifuging the pellet. One can also test different ratios of the lysis mix (Small RNA Lysis Buffer and Binding Solution).
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Can the mirPremier® microRNA Isolation Kit be used to isolate small RNAs from purified total RNA?
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We have used to the kit to purify in vitro transcribed small RNAs with great success, but have not done so with purified total RNA. Here are the steps we would recommend trying with purified total RNA:1. Prepare a lysis mix with 0.7 vol. Small RNA Lysis Buffer (M1070) and 0.3 vol. Binding Solution (L8042).2. Add 500 ul of lysis mix with 50 ul total RNA and mix thoroughly.3. Spin at 14000 rpm for 5 min to precipitate large RNA.5. Transfer the supernatant to a new tube.6. Add 610 ul (1.1 vol.) 100% ethanol to the supernatant and mix well.7.Transfer the mixture to a binding column and spin 1 min to bind. Repeat the binding step with the remaining mixture.8. Wash the column first with 700 ul 100% ethanol, and then with ethanol-diluted wash Solution 2.9. Dry the column and elute small RNA.
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Can I purify 18S and 28S large RNAs along with miRNAs with the mirPremier® microRNA Isolation Kit?
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Large RNAs (18S and 28S) from the pellet fraction can be purified after transferring the microRNA-containing supernatant to a new tube by using the total RNA protocol or by phenol/chloroform extraction.
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Has the mirPremier® microRNA Isolation Kit been tested on sperm cells?
1 answer-
We have not tested mirPremier™ microRNA Isolation Kit with sperm cells.
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