04823125001
Roche
High Pure FFPE RNA Micro Kit
kit of for 50 isolations
About This Item
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Allgemeine Beschreibung
Anwendung
- Qualitative RT-PCR
- Relative quantification of mRNA with real-time PCR systems such as the LightCycler® 480 System
- Differential display RT-PCR
- cDNA synthesis
- Primer extension
Leistungsmerkmale und Vorteile
Size Distribution: The typical size of RNA isolated from formalin-fixed tissue ranges from 150 to 1500 bases. However, section thickness, tissue type, age of sample, and the fixation protocol used can affect the yield and quality of the isolated RNA.
Capacity: The High Pure Micro Filter Tubes hold up to 500 μl sample volume.
Sample Material: 1 - 10 μm sections from formalin-fixed, paraffin-embedded (FFPE) tissue (e.g., from colon, breast, liver, kidney, spleen of mammalian species).
- Streamline and simplify RNA isolation (even small RNA fragments) from FFPE tissue.
- Obtain a highly concentrated, ready-to-use eluate and excellent recovery of RNA (>80%).
- Isolate DNA-free RNA for use in qualitative and quantitative RT-PCR.
- Minimize RNA loss with a kit that removes contaminants without precipitation or other handling steps that degrade RNA.
- Generate high-quality template RNA that shows excellent performance and linearity in RT-PCR.
Komponenten
- Tissue Lysis Buffer
- Proteinase K, recombinant, PCR Grade
- Binding Buffer
- Wash Buffer I
- Wash Buffer II
- DNase I, recombinant, lyophilized
- DNase Incubation Buffer
- Elution Buffer
- High Pure Micro Filter Tubes
- Collection Tubes
Qualität
The RNA eluate and specific primers for the ß2M gene are used in one-step RT-PCR. In the following PCR on the LightCycler® 2.0 Instrument (accomplished using the LightCycler® RNA Amplification Kit SYBR Green I and specific primers for β2M), the expected amplification signal is obtained at a Cp-value less than 24.
Absence of contaminating genomic DNA is examined by PCR on a LightCycler® 2.0 Instrument without a reverse transcriptase step; no amplification product is obtained.
Angaben zur Herstellung
Under the buffer conditions used in the procedure, all nucleic acids bind specifically to the glass fiber fleece, while contaminating substances (salts, proteins, and other tissue contaminants) do not. DNA in the preparation is digested with DNase I directly on the filter. Brief wash-and-spin steps readily remove the digested DNA fragments and other contaminating substances. The remaining purified RNA is then eluted in a small volume of low-salt buffer.
Hinweis zur Analyse
Starting Material and Quantity: 1 - 10 μm FFPE sections, colon, breast, liver, kidney, spleen of mammalian species
Yield/Recovery: 1.5 - 3.5 μg/5 μm section
Time Required: 60 minutes without 3 hour incubation
Number of Reactions: 50/1-10 μm sections
Rechtliche Hinweise
Signalwort
Danger
Gefahreneinstufungen
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Resp. Sens. 1 - Skin Corr. 1C - Skin Sens. 1 - STOT SE 3
Zielorgane
Respiratory system
Zusätzliche Gefahrenhinweise
Lagerklassenschlüssel
13 - Non Combustible Solids
WGK
WGK 2
Flammpunkt (°F)
does not flash
Flammpunkt (°C)
does not flash
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