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| NucleoSpin® RNA L |
Total RNA from cells and tissue
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| Features |
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| Complete midi kit with recombinant DNase and shredders for DNA-free* RNA of high quality |
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• rDNase included for on-column digestion ® efficient removal of genomic DNA
• NucleoSpin Filters L (shredders) included ® efficient homogenization and reduction of viscosity
• Up to 600 µg ready-to-use RNA
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| Technology |
Silica-membrane technology |
| Format |
Midi spin columns |
| Sample material |
< 5 x 107 cultured cells
< 1010 bacterial cells, up to 3 x 108 yeast cells
< 200 mg tissue
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| Fragment size |
200 b - 20 kb |
| Typical yield |
180 µg from 107 HeLa cells
620 µg from 4 x 107 HeLa cells
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| A260/280 |
1.9-2.1 |
| Typical RIN (RNA integrity number) |
> 9 |
| Elution volume |
500 µl |
| Preparation time |
80 min/4 preps |
| Binding capacity |
700 µg |
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Applications**
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• Total RNA isolation from cultured cells, tissue (standard protocol)
• Support protocol for total RNA from £ 1010 bacterial cells (Gram-negative and Gram-positive)
• Support protocol for total RNA from £ 3 x 108 yeast cells
• Support protocol for RNA clean-up from reaction mixtures
• Support protocol for total RNA from samples stored in RNAlater®
• RNA suitable for e.g. real-time RT-PCR, Northern bloting, primer extension, array technology, RNase
protection assays |
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* The amount of DNA contamination is significantly reduced during on-column rDNase digestion. Anyhow, in very sensitive applications it might be possible to detect traces of DNA. The eventuality of DNA detection with PCR increases with:
– the number of DNA copies per preparation: single copy target < plastidial/ mitochondrial target < cells transfected
with plasmid
– decreasing PCR amplicon size
** Kits to be used for research purposes only
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Ordering information
| Product |
Preps
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Specification |
Reference |
| NucleoSpin RNA L |
20
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NucleoSpin RNA L Columns with Collection Tubes
(15 ml), Collection Tubes (15 ml), NucleoSpin Filters L,
buffers, RNase-free rDNase |
740962.20 |
For ordering click here
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