AmpliScribe T7 High Yield Transcription Kit
Product Details
ShowAmpliScribe T7 Enzyme Solution, 100 mM ATP, CTP, GTP, and UTP Solutions, AmpliScribe 10X Reaction Buffer, 100 mM Dithiothreitol (DTT), RiboGuard RNase Inhibitor, RNase-Free Water, Control Template DNA, and RNase-Free DNase I
AmpliScribe T7 High Yield Transcription Kit
Key features
Show- Produce high yields of high quality RNA quickly and easily.
- Synthesise long and short RNA with one kit
- Produce 20 times more RNA than conventional or "homemade" in vitro transcription kits
Size: 50 reactions
Product information
The AmpliScribe™ T7 High Yield Transcription Kit is specially formulated to use high concentrations of NTPs, that can be inhibitory to other in vitro transcription systems. AmpliScribe High Yield Transcription reactions can produce >20-fold more full-length RNA transcript than conventional in vitro transcription reactions. For example, the AmpliScribe T7 Kit yields approximately 5-7.5 mg/ml of 1.4-kb full-length control RNA in 30-120 minutes, respectively, using 1 µg of template DNA (Figure. 1).
Applications
- High-yield synthesis of RNA from DNA cloned downstream from a T7 RNA polymerase promoter, for microinjection, RNA interference, or antisense experiments.
- Structural and functional studies of splicing, processing, heterogeneous nuclear RNAs, tRNAs, viral RNAs, and ribozymes. 1
- Production of fluorescent 2-, biotinylated 3-, or digoxigenin 4- labelled RNA.
Features
- High yield. Produce microgram amounts of RNA from all templates—synthesise both long (Figure. 2) and short RNA using only one kit. 5
- Sensitive. Produce microgram amounts of RNA from as little as 1 ng of template.
- Scalable. Increase the reaction size to produce milligram amounts of RNA.
- Flexible. Substitute a labelled nucleotide for one of the supplied NTP solutions.
- Convenient. RNase inhibitor included.
Note: Because of the very high concentration of NTPs used in AmpliScribe reactions, these kits are not recommended for preparing high specific-activity radiolabelled RNA probes.
References
- Johnson, M. (1995) Epicentre Forum 2(5), 4.
- DeLong, E.F. et al. (1999) App. And Environ. Microbiol. 65, 5554.
- Kaplan, E. et al. (1996) Epicentre Forum 3(2), 1.
- Hoff man, L.M. and Johnson, M.G. (1994) BioTechniques 17, 372.
- Schanke, J. (2000) Epicentre Forum 7(2), 6.
- Molecular Cloning - A Laboratory Manual, Third Edition, 2001. CSHL Press. pp 7.27 - 7.34. J. Sambrook and D. Russell.
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