- Isolate nuclear and cytoplasmic RNA and protein from cultured cells
- Isolate total RNA and protein from cultured cells or tissues
- No phenol extraction or alcohol precipitation
PARIS uses a fast, simple procedure
based on Ambion's RNAqueous® technology to isolate both
RNA and native protein from the same experimental sample. The
kit also permits separation of nuclear and cytoplasmic fractions
prior to RNA and/or protein isolation. The resulting protein
and RNA samples are suitable for various downstream applications,
reducing time, cost, and variability between independent experimental
samples.
Protein And RNA Isolation System (PARIS)
Isolation of high quality RNA is the first step for a variety of gene expression
analyses. Very often complementary studies at the protein level are also
required, e.g. performing further in vitro functional assays, analyzing a
regulatory pathway, or simply correlating RNA and protein expression levels.
Usually these analyses are performed using different aliquots of the same
experimental sample. However, when working with rare, difficult to obtain,
or very small samples it is sometimes impractical to isolate RNA and native
proteins independently. In studies involving large numbers of samples, expensive
reagents, or inherent variability (e.g. cell transfection), the addition
of independent experimental samples is not only costly and time consuming,
but may also lead to inconsistent results. To solve these issues Ambion scientists
have developed a unique Protein And RNA Isolation System (PARIS) that allows
researchers to isolate both RNA and protein from the same experimental sample
(see bottom figure at right).
Using PARIS, RNA and protein can
be isolated simultaneously from whole cell lysates. Alternatively,
RNA and protein can be
isolated from separate nuclear and cytoplasmic fractions. Tissue or
cultured cells are first homogenized in ice-cold Cell Disruption
Buffer
to prepare a total cell lysate. Since the homogenization is performed
quickly on ice and in the presence of detergent, both protein
and RNA can be purified directly from this lysate. For RNA isolation,
a part of the total cell lysate is immediately mixed with an
equal volume of Lysis/Binding Solution. This solution contains
a high concentration of guanidinium thiocyanate, a strong chaotropic
denaturant that rapidly inactivates cellular ribonucleases. Total
RNA is then purified from the mixture using an RNA binding glass
fiber filter. After three rapid washing steps, high quality RNA
is eluted in a concentrated form. The entire procedure can be
completed in less than 20 minutes. Note: This kit is not recommended
for tissues with high levels of ribonucleases, such as pancreas.
Compatible with Most Downstream Applications
The RNA isolated from total, nuclear, or cytoplasmic fractions with the PARIS
procedure can be used in a variety of downstream applications, including
blot hybridization, in vitro translation, cDNA synthesis, and RT-PCR. A DNase
I treatment is recommended for RNA that will be used for RT-PCR experiments,
especially if using primers that do not flank introns, or for genes that
have processed pseudogenes. Ambion's DNA-free™ DNase Treatment
and Removal Reagents (available separately) are ideal to quickly remove trace
amounts of DNA from the total and nuclear RNA samples without phenol extraction
or alcohol precipitation. The cytoplasmic RNA fraction is virtually free
of DNA contamination.
Each protein fraction can also be
used directly for most common applications, including functional
assays, immunoprecipitation,
Western blotting or two-dimensional gel electrophoresis (Figure
1 at right). For experiments such as gel shift assays or enzymatic
assays (Figure 2B), protein samples are usually concentrated
enough
to be diluted in the final reaction buffer. The Cell Disruption
Buffer and Cell Fractionation Buffer have been specially designed
to be compatible with downstream analyses.
The PARIS Kit includes sufficient reagent to perform 50 purifications.
The kit also comes with a comprehensive Instruction Manual and
RNase-free microfuge tubes, glass fiber filters and reagents
for RNA isolation. Each purification can accommodate 1 to 75
mg of tissue or 100 to 107 cells.
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