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"Name": "Storage Conditions (Product)",
"Value": "Store the kit at +15 to +25°C.",
"Language": "en",
"Country": "XG",
"Code": "Storage Conditions (Product)"
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{
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Solution | Storage |
Wash Buffer I | +15 to +25 °C |
Wash Buffer II | +15 to +25 °C |
Proteinase K | -15 to -25°C |
DNase I (reconstituted) | -15 to -25°C |
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"Value": "Kit for manual RNA isolation from FFPE tissue for subsequent analysis in PCR, arrays and NG-sequencing.",
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"Value": "The High Pure FFPET RNA Isolation Kit uses a fast and optimized technology for the isolation and purification of total RNA from formalin-fixed, paraffin-embedded tissue research samples. The quality of RNA from tissue samples is suitable for the following downstream applications:
- RT-PCR
- Gene Expression Array
- Next Generation Sequencing
- PreAmplification
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Vial / Bottle | Cap | Label | Function / Description | Content |
1 | red | RNA Tissue Lysis Buffer | | 6 ml |
2 | pink | Proteinase K, PCR grade | - Lyophilizate
- For sample homogenization and inactivation of endogenous nucleases
| 2 × 100 mg |
3 | green | RNA Binding Buffer | - Contains 5 M guanidine thiocyanate
Store protected from light | 20 ml |
4 | black | Wash Buffer I | - Contains 5 M guanidine HCl (final concentration after addition of ethanol)
| 25 ml, add 15 ml absolute ethanol |
5 | blue | Wash Buffer II | | 20 ml, add 80 ml absolute ethanol |
6 | white | DNase I | - Lyophilizate
- Contains 4 kU DNAse I
- For digestion of residual DNA
| 100 mg |
7 | white | DNase Incubation Buffer (1x) | | 6 ml |
8 | colorless | RNA Elution Buffer | | 5 × 1,000 μl |
9 | colorless | Reagent Preparation Buffer | | 11.5 ml |
10 | | High Pure Filter Tubes | | 50 polypropylene tubes with two layers of glass fiber fleece |
11 | | Collection Tubes | | 3 bags containing 50 polypropylene tubes (2 ml) |
All solutions are clear and should not be used when precipitates have formed. Warm the solutions at +15 to +25°C or in a 37°C water bath until the precipitates have dissolved.
The buffers can show a slight yellow color. This will have no impact on the function of the buffer
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"Name": "Assay Time",
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Total time | Approx. 2.5 hours including deparaffinization procedure |
---|
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"Code": "Assay Time"
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"Name": "Principle",
"Value": "FFPE tissue samples are disrupted and homogenized during incubation with RNA Tissue Lysis Buffer and Proteinase K. Nucleic Acids (NA) bind in the presence of a chaotropic salt specifically to the surface of glass fibers pre-packed in the High Pure Purification Filter Tube.
RNA is purified in a series of rapid \"wash-and-spin\" steps to remove salts, proteins, and cellular components. Residual DNA is digested on the column by adding DNase I.
Finally, a low-salt elution releases the RNA from the glass fiber. The process does not require RNA precipitation or organic solvent extraction, ideal for rapidly purifying many samples simultaneously.
- Samples are disrupted in RNA Tissue Lysis Buffer and homogenized during an incubation with Proteinase K.
- In the presence of chaotropic salt, nucleic acids (NA) bind specifically to the surface of glass fibers pre-packed in the High Pure Filter Tube.
- To eliminate residual DNA, an on-column DNase I digestion is performed
- Bound RNA is washed, and thereby purified of salts, proteins, and other impurities.
- For the final step, a low-salt elution releases the RNA from the glass fibers.
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"Name": "Product Purpose",
"Value": "Kit for manual RNA isolation from FFPE tissue for subsequent analysis in PCR, arrays and NG-sequencing.",
"Language": "en",
"Country": "XG",
"Code": "Product Purpose"
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