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DMN10
GenElute™ Direct mRNA Miniprep Kits
sufficient for 10 purifications
Synonym(e):
GenElute™ Direct mRNA Miniprep Kit, GenElute™ mRNA Kit, Gen Elute
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273,00 €
Voraussichtliches Versanddatum07. Mai 2025
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About This Item
273,00 €
Voraussichtliches Versanddatum07. Mai 2025
Empfohlene Produkte
Verwendung
sufficient for 10 purifications
Qualitätsniveau
Methode(n)
RNA purification: suitable
Lagertemp.
15-25°C
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Allgemeine Beschreibung
For direct mRNA preparation, cells or tissues are disrupted with SDS/proteinase K digestion to release RNA and eliminate RNases. The kit uses oligo (dT) 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.
Up to 107 mammalian cells or 40 mg tissue are lysed and homogenized, either with the filtration columns provided or with a mechanical homogenizer. RNase is eliminated during a 10 minute proteinase K digestion. Sodium chloride is added, and polyadenylated RNA is captured on oligo(dT) polystyrene beads during a 10 minute incubation. For further enrichment, RNA may be released from the beads into fresh lysis solution and recaptured with the original beads. After 3 washes in a spin column, purified mRNA is eluted in 100 μL of 10 mM Tris-HCl, pH 7.4.
The purified mRNA is ready for Northern analysis, reverse transcription and PCR, labeling for arrays, and other common applications.
a mechanical homogenizer. RNase is eliminated during a 10 minute proteinase K digestion. Sodium chloride is added, and polyadenylated RNA is captured on oligo(dT) polystyrene beads during a 10 minute incubation. For further enrichment, RNA may be released from the beads into fresh lysis solution and recaptured with the original beads. After 3 washes in a spin column, purified mRNA is eluted in 100 μl of 10 mM Tris-HCl, pH 7.4.
Anwendung
Leistungsmerkmale und Vorteile
- Poly (A)+ mRNA isolated from total RNA in 40 minutes or 60 minutes directly from cells and tissues
- Oligo(dT) polystyrene beads require fewer wash steps
- mRNA captured on oligo(dT) polystyrene beads in 10 minutes, with no mixing or rocking
- mRNA captured on oligo(dT) polystyrene beads in 10 minutes, with no mixing or rocking (Fig. 1)
- Poly (A)+ mRNA isolated from total RNA in 40 minutes (Fig. 2) or 60 minutes directly from cells and tissues (Fig. 3)
- Oligo(dT) polystyrene beads require fewer wash steps
Sonstige Hinweise
Rechtliche Hinweise
Nur Kit-Komponenten
- Elution solution 1.5 mL
- Filtration columns with tubes 10 ea
- Lysis solution 20 mL
- 5 M NaCl 1.5 mL
- Oligo(dT)-polystyrene beads .3 mL
- Proteinase K 5 mg
- 40% Glycerol solution .6 mL
- Spin columns with tubes 10 ea
- Collection tube 10 ea
Signalwort
Danger
H-Sätze
Gefahreneinstufungen
Eye Irrit. 2 - Met. Corr. 1 - Resp. Sens. 1 - Skin Irrit. 2 - STOT SE 3
Zielorgane
Respiratory system
Lagerklassenschlüssel
8A - Combustible corrosive hazardous materials
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
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Protokolle
Method for reverse transcription of RNA into DNA. Uses a premixed reagent that contains reverse transcriptase, dNTPs, primers, RNase inhibitor and buffer. Fast generation of cDNA.
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