DMN10
GenElute™ Direct mRNA Miniprep Kits
sufficient for 10 purifications
Synonym(s):
GenElute™ Direct mRNA Miniprep Kit, GenElute™ mRNA Kit, Gen Elute
About This Item
Recommended Products
usage
sufficient for 10 purifications
technique(s)
RNA purification: suitable
storage temp.
15-25°C
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General description
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.
Application
Features and Benefits
- 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
Other Notes
Legal Information
Kit Components Only
- 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
signalword
Danger
hcodes
Hazard Classifications
Eye Irrit. 2 - Met. Corr. 1 - Resp. Sens. 1 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
8A - Combustible corrosive hazardous materials
flash_point_f
Not applicable
flash_point_c
Not applicable
Certificates of Analysis (COA)
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Protocols
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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