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Merck

SNC50

mirPremier® microRNA Isolation Kit

1 sufficient for 50 preparations

Synonim(y):

microRNA Isolation Kit

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1 KIT

1770,00 zł

1770,00 zł


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Informacje o tej pozycji

NACRES:
NA.52
UNSPSC Code:
41105501

Przejdź do

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technique(s)

DNA extraction: suitable

usage

sufficient for 50 preparations

Quality Level

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1 of 4

Ta pozycja
SNC10RTN350RTN70
usage

sufficient for 50 preparations

usage

sufficient for 10 preparations

usage

sufficient for 350 purifications

usage

sufficient for 70 purifications

technique(s)

DNA extraction: suitable

technique(s)

DNA extraction: suitable

technique(s)

RNA purification: suitable

technique(s)

RNA purification: suitable

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

SNC10

SNC50

RTN10, RTN70, RTN9602, RTN9604

RTN10, RTN350, RTN9602, RTN9604

General description

Sigma′s mirPremier microRNA Isolation Kit provides a rapid and efficient method for purifying and enriching miRNAs and other small RNAs from diverse biological sources, including mammalian cell cultures, animal tissues, plant tissues, and microbial cultures, without using hazardous organic extractions. microRNAs (miRNAs) are a class of small RNA molecules, about 21 nucleotides (nt) in length, that regulate gene expression in a variety of manners, including translational repression, mRNA cleavage and deadenylation. In addition, the kit also can be used for isolating total RNA if messenger RNA or other large RNAs are of interest.
.

Application

mirPremier® microRNA Isolation Kit has been used to:

  • 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

mirPremier is a registered trademark of Merck KGaA, Darmstadt, Germany
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Tylko elementy zestawu

Numer produktu
Opis

  • Binding Solution 2

  • Lysis Solution

related product

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2

Klasa składowania

10 - Combustible liquids

flash_point_f

Not applicable

flash_point_c

Not applicable

wgk

WGK 3


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Masz już ten produkt?

Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Jon Bråte et al.
Current biology : CB, 28(20), 3288-3295 (2018-10-16)
The emergence of multicellular animals was associated with an increase in phenotypic complexity and with the acquisition of spatial cell differentiation and embryonic development. Paradoxically, this phenotypic transition was not paralleled by major changes in the underlying developmental toolkit and
Unicellular origin of the animal microRNA machinery
Br?te J, et al.
Current Biology, 28(20), 3288- 3295 (2018)
Abdulla Abdulla Sabana et al.
Planta, 251(4), 79-79 (2020-03-14)
Genome-wide analysis of small RNAs identifies somatic embryogenesis- specific miRNAs and their targets and provides novel insights into the mechanisms governing somatic embryogenesis in coconut, a highly in vitro recalcitrant species. Coconut, a major plantation crop of the tropics is
Rong-Hua Lu et al.
Fish physiology and biochemistry, 46(5), 1665-1677 (2020-05-25)
Hepatic lipid metabolism disorder due to excessive fat accumulation in fish is a significant problem in aquaculture. Studies have shown that grape seed procyanidin extract (GSPE) can regulate fish lipid metabolism and improve fish immunity. However, the mechanism is unclear.
Interspecies communication between plant and mouse gut host cells through edible plant derived exosome-like nanoparticles.
Mu J
Molecular Nutrition And Food Research, 58(7), 1561-1573 (2014)

Produkty

Proste metody oczyszczania DNA/RNA wspomagają analizę genomu z różnych źródeł, zwiększając efektywność badań.

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

Powiązane treści

Sigma-Aldrich® Advanced Genomics is the leading provider of gene editing and silencing technologies including CRISPR, Cas9, synthetic guide RNA (sgRNA), and Zinc Finger Nuclease (ZFN).

Sigma-Aldrich® Advanced Genomics jest wiodącym dostawcą technologii edycji i wyciszania genów, w tym CRISPR, Cas9, syntetycznego RNA prowadzącego (sgRNA) i Zinc Finger Nuclease (ZFN).

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Questions

1–5 of 5 Questions  
  1. Methanol 100% can be used for the dilution of the wash solution instead of ethanol 100%?

    1 answer
    1. 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

      Helpful?

  2. Can the mirPremier® microRNA Isolation Kit be used to isolate small RNAs from purified total RNA?

    1 answer
    1. 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.

      Helpful?

  3. Has the mirPremier® microRNA Isolation Kit been tested on sperm cells?

    1 answer
    1. We have not tested mirPremier™ microRNA Isolation Kit  with sperm cells.

      Helpful?

  4. How can I avoid co-purifying mRNAs and rRNAs when purifying small RNAs from gram negative bacteria using mirPremier® microRNA Isolation Kit?

    1 answer
    1. 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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  5. Can I purify 18S and 28S large RNAs along with miRNAs with the mirPremier® microRNA Isolation Kit?

    1 answer
    1. 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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