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Thermo Scientific™ RapidOut DNA Removal Kit
Description
Includes
- DNase I, RNase-free (1U/μL) - 250Lμ
- 10X Reaction Buffer with MgCl2 - 1mL
- DNase Removal Reagent (DRR) - 500μL
- Water, nuclease-free - 2 x 1.25mL
Thermo Scientific RapidOut DNA Removal Kit rapidly and safely removes genomic DNA from total RNA and mRNA preparations. Complete digestion of DNA and safe removal of DNase I from the digestion reaction is ensured without RNA damaging steps, such as heating or organic extraction. First, the RNA sample is treated with recombinant RNase-free DNase I to levels below the limit of detection by routine PCR. DNase I is safely removed subsequently using proprietary DNase Removal Reagent (DRR).
DRR efficiently binds DNase I and the complex is collected at the bottom of the tube by centrifugation. The purified RNA is collected as a supernatant. The RNA after RapidOut procedure is free from DNA contamination and free of DNase I. It is ready to use in different applications including end-point or real-time RT-PCR, cloning, microarrays, and Northern blotting.
Highlights
• Efficient—complete ds and ssDNA digestion and proprietary technology for DNase I removal
• Rapid—single step sufficient for complete DNase I removal
• Safe—no need for toxic organic extractions or RNA-damaging heating steps
Main Applications
• RNA isolation and RNA analysis, particularly RT-qPCR and RT-PCR (customers performing expression analysis of low transcription level genes.
• Customers performing ds-cDNA synthesis from total RNA preps.
Other applications
• Elimination of DNA from RNA for microinjections and transfection.
• Elimination of DNA from RNA prior microarray analysis.
• Elimination of DNA from RNA prior Northern blot analysis.
Specifications
Specifications
| Enzyme | DNase |
| Quantity | 50 preps |
| Product Type | Removal Kit |
Frequently Asked Questions (FAQs)
RNA recovery after the RapidOut DNA removal procedure is high. Typically it is higher than conventional DNAse I inactivation methods such as heat, EDTA or chloroform/phenol extraction.
We have tested the kit for DNase I removal only. Although DRR can bind to other proteins, we cannot provide any recommendations for removal of protein contaminants from the enzymatic mixtures. If the RNA sample contains a considerable amount of protein contaminants, modify the RNA purification protocol to reduce protein contamination.
For Research Use Only. Not for use in diagnostic procedures.
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