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Description
Includes
T7 Express Enzyme Mix; RiboMAX Express T7 2X Buffer; pGEM Express Positive Control Template; Sodium Acetate, 3.0M (pH 5.2); RNase A Solution; RQ1 RNase-free DNase; Nuclease-free Water
- Produces Milligam Amounts of RNA for RNA Interference Experiments
- siRNA duplexes for mammalian RNAi
- Long dsRNA for nonmammalian RNAi
- Produces milligram amounts of double-stranded RNA in 30 minutes
- U.S. Patent 5,552,302.
- This product is covered under license from Carnegie Institution of Washington under U.S. Patent 6,506,559, Australian Patent 743798 and other patents pending. Commercial use of this product will require a separate license from Carnegie.
Specifications
Specifications
| Content And Storage | -30°C to -10°C |
| For Use With (Application) | Synthesis of siRNA duplexes for mammalian RNA interference, generation of large quantities of long dsRNA for non-mammalian RNA interference |
| Includes | 100μL Enzyme mix, T7 Express (T7 RNA Polymerase, recombinant RNasin™ RNase inhibitor and recombinant inorganic Pyrophosphatase), 500μL RiboMAX™ Express T7 2X Buffer, 110U 1U/ |
| Quantity | 50 x 20 μL |
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