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04823125001

Roche

High Pure FFPE RNA Micro Kit

kit of for 50 isolations

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About This Item

Code UNSPSC :
41105500
Nomenclature NACRES :
NA.55

Niveau de qualité

Fabricant/nom de marque

Roche

Conditionnement

kit of for 50 isolations

Catégories apparentées

Description générale

Low to medium throughput isolation of total RNA from free FFPE tissue sections in micro scale.

Application

The High Pure FFPE RNA Micro Kit isolates total RNA from formalin-fixed, paraffin-embedded (FFPE) tissue samples for direct use in:

  • 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

Caractéristiques et avantages

Nucleic acids bind to the surface of the glass fiber fleece in the presence of a chaotropic salt (guanidine HCl). This allows the High Pure filter tube to specifically immobilize nucleic acids (both DNA and RNA) while they are freed of contaminants. For RNA isolation, the binding conditions can be optimized to ensure immobilization of all the RNA.

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).
The High Pure FFPE RNA Micro Kit isolates total RNA from formalin-fixed, paraffin-embedded (FFPE) tissue samples for direct use in RT-PCR.

  • 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.

Composants

  • 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

Qualité

Formalin-fixed, paraffin-embedded tissue sections are homogenized by overnight Proteinase K digestion and purified as described. RNA yield is determined by measuring the optical density at 260 nm.
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.

Notes préparatoires

To prepare tissue sections for RNA isolation, fixation reagents must be removed from the samples; after deparaffinization, the sections are ready to be processed with the High Pure FFPE RNA Micro Kit. Deparaffinized tissue samples are disrupted and homogenized during incubation with Proteinase K and a chaotropic salt (guanidine HCl). The homogenate is then applied to the glass fiber fleece in a High Pure Micro Filter Tube.

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.

Remarque sur l'analyse

Typical RNA Recovery

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

Autres remarques

For general laboratory use.

Informations légales

LightCycler is a registered trademark of Roche

Pictogrammes

CorrosionExclamation markHealth hazard

Mention d'avertissement

Danger

Classification des risques

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

Organes cibles

Respiratory system

Risques supp

Code de la classe de stockage

13 - Non Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

does not flash

Point d'éclair (°C)

does not flash


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Isabella Wimmer et al.
Scientific reports, 8(1), 6351-6351 (2018-04-22)
Formalin-fixed paraffin-embedded (FFPE) tissues are valuable resources commonly used in pathology. However, formalin fixation modifies nucleic acids challenging the isolation of high-quality RNA for genetic profiling. Here, we assessed feasibility and reliability of microarray studies analysing transcriptome data from fresh
Zachary Kerr et al.
Head and neck pathology, 14(3), 577-587 (2019-09-14)
Kallikrein-related peptidases (KLKs) are a group of 15 serine proteases implicated in a variety of biological processes. Aberrant expression of KLKs has been associated with the development of certain cancers. However, the role of KLKs in salivary tumors has not
George P Christophi et al.
Experimental and molecular pathology, 96(3), 393-399 (2014-04-29)
Sarcoidosis is an immune-mediated multisystem disease characterized by the formation of non-caseating granulomas. The pathogenesis of sarcoidosis is unclear, with proposed infectious or environmental antigens triggering an aberrant immune response in susceptible hosts. Multiple pro-inflammatory signaling pathways have been implicated
David S Shames et al.
Clinical cancer research : an official journal of the American Association for Cancer Research, 19(24), 6912-6923 (2013-10-08)
We sought to identify predictive biomarkers for a novel nicotinamide phosphoribosyltransferase (NAMPT) inhibitor. We use a NAMPT inhibitor, GNE-617, to evaluate nicotinic acid rescue status in a panel of more than 400 cancer cell lines. Using correlative analysis and RNA
Inês Pires da Silva et al.
Clinical cancer research : an official journal of the American Association for Cancer Research, 25(4), 1272-1279 (2019-01-12)
BRAF V600E and V600K melanomas have distinct clinicopathologic features, and V600K appear to be less responsive to BRAFi±MEKi. We investigated mechanisms for this and explored whether genotype affects response to immunotherapy. Pretreatment formalin-fixed paraffin-embedded tumors from patients treated with BRAFi±MEKi

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