RNAzol®RT
RNAzol®RT is the most effective reagent for isolation of total RNA and small RNA from samples of human, animal, plant, bacterial and viral origin. This patent-pending reagent(1) provides higher yield and quality of isolated RNA than previous reagents based on the single-step method. RNAzol RT isolates pure and undegraded RNA that is ready for RT-PCR without DNase treatment.(2)
- No chloroform-induced phase separation is necessary to obtain pure RNA. Just add water to remove DNA, proteins, polysaccharides and other contaminants.
- The isolation procedure can be completed in less than one hour and is performed at room temperature, including all centrifugation steps.
- RNAzol RT isolates total RNA, with mRNA and small RNA in separate fractions. Small RNA contains RNA < 200 bases, including 10 - 40 base miRNA.
- The isolated RNA is ready for RT-PCR, qRT-PCR, microarrays, poly A+ selection, northern blotting, RNase protection assay and other molecular biology applications.
- Due to the removal of impurities, the RNA pellets are smaller and solubilize more easily than pellet obtained from previous single-step reagents.
- In addition, RNAzol RT allows for the simultaneous isolation of RNA and DNA.
RNAzol® RT is used to isolate RNA from tissues, cells, liquid samples or blood. One milliliter is sufficient
CAT # | VOL |
| RN 190 | 50 ml 100 ml 200 ml 500 ml |
to process up to 100 mg tissue yielding 50 - 700 µg of large RNA (>200 bases)
and 8 - 120 µg of small RNA (200 - 10 bases).
References
1. Chomczynski, P., Reagents and methods for isolation of purified RNA, US and International Patents Pending.
2. Chomczynski, P. and Sacchi, N. Single-step method of RNA isolation by acid guanidinium
thiocyanatephenol-chloroform extraction. Anal. Biochem. 162: 156-159. 1987.
Agilent RNA Nano Chip and Small RNA Chip analysis of rat liver total RNA (A) and
small RNA (B), respectively. High quality total RNA had a RIN value of 9.2 and
28/18 S ratio of 1.6. miRNA region (B, inset) represents about 5% of small RNA.
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Last modified: June 16, 2010
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