MRN70
GenElute™ mRNA Miniprep Kit
sufficient for 70 purifications
Sinônimo(s):
GenElute™ mRNA Kit, Gen Elute
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1 KIT
R$ 5.586,00
R$ 5.586,00
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1 KIT
R$ 5.586,00
About This Item
Código UNSPSC:
41105501
NACRES:
NA.52
R$ 5.586,00
Check Cart for Availability
Produtos recomendados
uso
sufficient for 70 purifications
técnica(s)
RNA purification: suitable
temperatura de armazenamento
15-25°C
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Categorias relacionadas
Descrição geral
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.
Aplicação
The purified mRNA is ready for Northern analysis, reverse transcription and PCR, labeling for arrays, and other common applications.
Características e benefícios
- 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
Outras notas
For additional information, please see www.sigma-aldrich.com/mrna.
Informações legais
GenElute is a trademark of Sigma-Aldrich Co. LLC
Código de classe de armazenamento
10 - Combustible liquids
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Methyltransferase-like 3 (METTL3) and N6-methyladenosine (m6A) are involved in many types of biological and pathological processes, including DNA repair. However, the function and mechanism of METTL3 in DNA repair and chemotherapeutic response remain largely unknown. In present study, we identified
Adrenal gland-dependent augmentation of plasminogen activator inhibitor-1 expression in streptozotocin-induced diabetic mice.
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K Oishi et al.
Journal of thrombosis and haemostasis : JTH, 4(7), 1566-1574 (2006-07-15)
Diabetes is associated with an excess risk of cardiac events, and one risk factor for infarction is an elevated level of plasminogen activator inhibitor-1 (PAI-1). To evaluate whether the glucocorticoid hormones are involved in the diabetes-induced PAI-1 production, we examined
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Cell, 178(3), 731-747 (2019-07-02)
N6-methyladenosine (m6A) is the most abundant modification on mRNA and is implicated in critical roles in development, physiology, and disease. A major limitation has been the inability to quantify m6A stoichiometry and the lack of antibody-independent methodologies for interrogating m6A.
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