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Key Documents

SCR703

Sigma-Aldrich

Human OKSG-cMyc Simplicon® RNA

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About This Item

Kod UNSPSC:
12352207
eCl@ss:
32161000
NACRES:
NA.51

metody

cell culture | stem cell: suitable

Poziom jakości

moc wejściowa

sample type induced pluripotent stem cell(s)

Warunki transportu

ambient

Opis ogólny

Various methods utilizing viruses, DNA, RNA, miRNA and protein have been developed to generate integration-free induced pluripotent stem cells (iPSCs). Disadvantages to existing methods include: (1) low reprogramming efficiency (i.e. DNA and protein), (2) a lengthy requirement for negative selection and subcloing steps to remove persistent traces of the virus (i.e. Sendai virus)1 and (3) daily transfections of cells using four synthetic mRNAs over a 14 day period (i.e. mRNA based).

EMD Millipore′s Simplicon® OKSG-cMyc RNA uses a safe and efficient method to generate integration- and virus-free human iPSCs using a single transfection step. The technology utilizes a single self-replicating Venezuelian equine encephalitis (VEE) RNA species that expresses reprogramming factors (RF) ORFs3. The Simplicon RNA replicon is a synthetic polycistronic VEE-RF RNA expressing five reprogramming factors (OKSG-cMyc; Oct4, Klf4, Sox2, Glis1 and cMyc), capable of self-replicating in a limited number of cell divisions. The 5-factor OKSG-cMyc Simplicon is especially useful for iPSCs generation from somatic cells that are more difficult to reprogram (i.e. slower proliferating cells or aged somatic cells).

Zastosowanie

Advantages of the Simplicon® OKSG-cMyc RNA:

  • Integration-free, footprint-free iPSCs generation. No risk of genomic integration.
  • Safe, virus-free, synthetic polycistronic RNA replicon (all five reprogramming factors in a single RNA strand)
  • Only one single transfection required. The RNA replicon is able to self-replicate, eliminating the need for additional daily transfections of multiple individual mRNAs over a 14-day period.
  • Efficient and rapid reprogramming.
  • No screening required to ensure the absence of viral remnants.
  • Controlled elimination of synthetic VEE RNA replicon by the removal of B18R protein.
  • Validated for reprogramming in feeder-free and feeder-based culture conditions.
Research Category
Stem Cell Research

Komponenty

1. VEE-OKSG-cMyc RNA: (Part No. CS221303) One (1) vial containing 10 L of RNA (1 ug/uL). Store at -80°C.

2. B18R-E3L RNA: (Part No. CS224503) One (1) vial containing 10 L of RNA (1 ug/uL). Store at -80°C.

Jakość

Tested to confirm the generation of iPS cells from p6 human foreskin fibroblasts. Other cell types have not been tested and thus similar results can not be guaranteed.

Przechowywanie i stabilność

VEE-OKSG-cMyc and B18R RNAs: Stable for 4 months from date of receipt when stored appropriately at -80°C. For best recovery, quick-spin the vial after thawing on ice and prior to opening. Aliquot into sterile, nuclease-free eppendorf tubes on ice and store at -80°C. Limit repeated freeze-thaw cycles. Use in a sterile RNase-free environment.

Informacje prawne

SIMPLICON is a registered trademark of Merck KGaA, Darmstadt, Germany

Oświadczenie o zrzeczeniu się odpowiedzialności

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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Kod klasy składowania

12 - Non Combustible Liquids

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable


Certyfikaty analizy (CoA)

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

Odwiedź Bibliotekę dokumentów

Enhanced generation of iPSCs from older adult human cells by a syntheticfive-factor self-replicative RNA.
Naohisa Yoshioka
Testing null

Protokoły

Stem cell reprogramming protocols to generate human induced pluripotent stem cells (iPSCs) including viral and non-viral RNA based methods.

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