Catalog number : BM0080-2000
Size : 2,000u (kunitz,25°C), 1ml
Concentration: 2u/ul
RNase activity: None-detected
Store at -20°C |
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| Description: |
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DNase I is purified from bovine pancreas that degrades single-stranded or double-stranded DNA to produce 3-hydroxyl oligonucleotides. This enzyme is used in molecular biology techniques like digestion of DNA, in the RNA isolation, nick translation and DNase I footprinting. |
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| Storage buffer: |
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10mM HEPES (pH7.5)
10mM CaCl2
10mm MgCl2
50% glycerol |
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| 10X Reaction Buffer: |
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400mM Tris-HCl ( pH8.0 )
100mM MgSO4
10mM CaCl2 |
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| Heat Inactivation ( Not for RT ): |
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Add EDTA solution (pH8.0) to final 2mM, heat at 75°C for 10 min. |
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| DNase I Treatment of RNA for RT-PCR |
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- Add the following components to a sterile, RNase-free tube. Keep the tube on ice during pipetting.
| RNA in water |
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1 -8μl |
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| 10X RNase-free DNase I buffer |
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1μl ( 10X composition: 400mM Tris-HCl (pH 8.0), 100mM MgSO4 and 10mM CaCl2.) |
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| RNase-free DNase I |
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1u/μg RNA |
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| Add RNase-free water to 10μl |
- Incubate at 37°C for 30 min.
- Incubate at 70°C for 5 min to inactivate the DNase.
- Add the treated RNA to the RT-PCR reaction.
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