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Nucleic acids have been utilized in research
labs for years to facilitate the prediction and detection of
disease. The use of molecular technology is now extending to
standard diagnostic assays. Whatman provides a comprehensive
range of fibrous materials and microplates for sample collection
and processing, as well as membranes for detection systems.
Features and Benefits
- Superior test-to-test reproducibility and
reliability.
Ensure consistent performance within and between lots.
- No sample contamination.
Whatman high-purity products are manufactured in controlled
environments from the highest quality raw materials.
- RNA and/or DNA storage.
Whatman FTA matrix will stabilize both RNA and DNA.
Broad Applicability Across Applications
The evolving market for molecular diagnostic products represents
an excellent opportunity for companies seeking to capitalize on
exciting new applications. Here is a small sampling of ways your
company can adopt pioneering Whatman technology to build sales.
RNA virus detection.
FTA-treated materials will enable RNA to be collected and
stabilized for up to 12 months (assuming proper storage
conditions). The RNA can then be purified by a simple procedure
before being released into solution, allowing the use of
standard amplification and detection techniques. Now it is
possible to test for viral RNA from whole blood samples
utilizing a very simple protocol.
Neonatal screening.
Currently, all neonatal applications screen for inherited
conditions by testing for proteins. However, testing neonate DNA
has significant advantages - most notably the ability to
increase the number of conditions being evaluated. The use of
BFC180 (if the DNA is to be used quickly) or FTA (if the DNA is
to be used subsequent to storage) will allow nucleic acid-based
detection.
Cellular purification.
Sensitivity is one of the biggest problems in many assays. In
essence, the presence of large amounts of human DNA (that is
found in leukocytes) can significantly reduce sensitivity.
Whatman produces materials that allow smaller cells or plasma to
be purified. These cells can then be lysed and the DNA or RNA
tested in the absence of human DNA. This technique has been
shown to work with Malaria assays, whereby erythrocytes are
collected before lyses. The sensitivity of the assay increases
tenfold, as opposed to the use of whole blood. This same idea
should work with any cell or organism that is smaller than white
cells. As such, viral particles, bacteria or protozoa could be
similarly isolated. |