Clinical Laboratory News - American Association for Clinical ...
Clinical Laboratory News - American Association for Clinical ...
Clinical Laboratory News - American Association for Clinical ...
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has a large touch-screen user interface and<br />
reads a standard 96-well microplate in less<br />
than 15 seconds. The versatile open system<br />
features cutoff modes, point-to-point, and<br />
regression calculations. It prints results on<br />
the internal thermal printer or outputs<br />
results to a PC to create custom-<strong>for</strong>matted<br />
reports.<br />
Awareness Technology, Inc.<br />
Circle No. 359 in the Reader Service Card<br />
MINICAP Automated SPE<br />
With a small footprint, the MINICAP instrument<br />
is designed to optimize and completely<br />
automate electrophoresis testing in low- to<br />
medium-volume laboratories. Simply place<br />
a bar-coded primary tube on the system<br />
and walk away. A continuous-access sample<br />
wheel allows <strong>for</strong> the addition of samples<br />
at any time, and true-positive sample ID is<br />
achieved with full traceability. The MINICAP<br />
Protein 6 assay is FDA cleared <strong>for</strong> separation<br />
and quantitation of the six major serum<br />
protein fractions by capillary electrophoresis..<br />
The MINICAP reagent compartment<br />
accommodates multiple assay buffers in<br />
anticipation of future menu expansion.<br />
Sebia Electrophoresis<br />
Circle No. 360 in the Reader Service Card<br />
STA Satellite® Analyzer<br />
The STA Satellite, the newest addition to the<br />
STA® family of analyzers, is a fully-automated<br />
benchtop coagulation analyzer capable of<br />
simultaneously per<strong>for</strong>ming clotting, chromogenic,<br />
and immunological assays. The STA<br />
Satellite analyzer offers complete automation<br />
<strong>for</strong> low-to- medium-activity coagulation labs<br />
and is suitable as a backup analyzer <strong>for</strong> organizations<br />
with central and satellite labs. It offers<br />
technological advances to ensure a high<br />
level of system reliability, ease of operation,<br />
and flexibility—all within a small footprint.<br />
Diagnostica Stago, Inc.<br />
Circle No. 361 in the Reader Service Card<br />
Calibrated Automated<br />
Thrombogram® Assay*<br />
The Calibrated Automated Thrombogram,<br />
or CAT, is an exciting new technology using<br />
a fluorogenic substrate in an easy-to-use automated<br />
plat<strong>for</strong>m to measure the initiation,<br />
burst, and subsequent inactivation of thrombin<br />
in clotting platelet-poor or platelet-rich<br />
plasma. It is a global hemostasis assay <strong>for</strong> the<br />
investigation of hypo- and hyper-coagulability<br />
and the effects of anti-thrombotics and<br />
28 CliniCal laboratory news JuLy 2008<br />
2008 NEw Pr o d u c t rE v i E w<br />
other pharmaceuticals on thrombin generation.<br />
A unique thrombin calibrator eliminates<br />
potential sample-specific interferences,<br />
such as the inner filter effect, substrate depletion,<br />
and variability in sample color and light<br />
intensity. Diagnostica Stago, Inc. represents<br />
Thrombinoscope as the exclusive distributor<br />
in the U. S. *For research use only.<br />
Diagnostica Stago, Inc.<br />
Circle No. 362 in the Reader Service Card<br />
STA® Liatest® FM Assay*<br />
The STA Liatest FM is an immunoturbidimetric<br />
assay <strong>for</strong> the quantitative determination<br />
of soluble fibrin monomer complexes<br />
(SFMC) on the STA line of analyzers. The<br />
test uses microparticles coated with monoclonal<br />
antibodies specific <strong>for</strong> SFMC that are<br />
mixed with the test plasma. The presence of<br />
SFMC causes agglutination of the microparticles,<br />
resulting in a change in absorbance<br />
that is measured at 540nm. High plasma levels<br />
of SFMC are usually observed in patients<br />
with disseminated intravascular coagulation<br />
(DIC). STA Liatest FM Calibrator and STA<br />
Liatest FM Control complete the Liatest FM<br />
product line. *For research use only.<br />
Diagnostica Stago, Inc.<br />
Circle No. 363 in the Reader Service Card<br />
STA® Control LA 1+2<br />
STA Control LA 1+2 are a lupus anticoagulant<br />
(LA) positive and negative control material.<br />
The two levels of assayed controls are <strong>for</strong><br />
use with the STA Staclot dRVV Screen and<br />
Confirm using the STA line of instruments.<br />
The controls are available in 1-mL vials with<br />
an onboard stability of 8 hours when used<br />
on the STA line of instrumentation.<br />
Diagnostica Stago, Inc.<br />
Circle No. 364 in the Reader Service Card<br />
STA® -Staclot® dRVV Screen<br />
and Confirm Assays<br />
The STA-Staclot dRVV Screen and Confirm<br />
are fully-automated assays <strong>for</strong> the detection<br />
of lupus anticoagulants (LA) in patient<br />
plasma by the diluted Russell viper venom<br />
method. Each reagent is bar coded <strong>for</strong> ease<br />
of use on the STA line of analyzers. The STA<br />
Staclot dRVV Screen assay uses a reagent<br />
with a low phospholipid concentration that<br />
enhances its sensitivity, resulting in a<br />
prolongation of the clotting time. The STA<br />
Staclot dRVV Confirm assay uses a reagent<br />
with a high phospholipid concentration that<br />
neutralizes the LA present in the plasma,<br />
resulting in a shortening of the clotting time.<br />
Diagnostica Stago, Inc.<br />
Circle No. 365 in the Reader Service Card<br />
ABL80 FLEX CO-OX Instrument*<br />
The ABL80 FLEX CO-OX incorporates the<br />
patented oximetry technology found in<br />
Radiometer’s benchtop analyzers, making<br />
it available in a portable, cartridge-based<br />
instrument. Radiometer’s ultra-sonic<br />
hemolyzation is well-established as superior<br />
to chemical hemolyzation, demonstrating<br />
superior measurement per<strong>for</strong>mance and<br />
zero risk of contamination from chemical<br />
agents. The ABL80 FLEX CO-OX offers<br />
the portability and ease-of-use advantages<br />
already benefiting users of the ABL80 FLEX<br />
plat<strong>for</strong>m. Its small footprint, rapid start-up,<br />
and fast measurement time make it ideal <strong>for</strong><br />
use in clinical areas, while full connectivity<br />
and auto QC ensure the lab maintains<br />
control of the testing process. *Pending FDA<br />
clearance.<br />
Radiometer America, Inc.<br />
Circle No. 366 in the Reader Service Card<br />
Little Dipper Processor <strong>for</strong> FISH<br />
From day one, this robotic system automates<br />
processing of FISH samples using Vysis or<br />
other probes, including post-hybridization<br />
steps. The Little Dipper processor provides<br />
precise temperature control and washing action<br />
that enhances test results and day-to-day<br />
reproducibility. It also can be used <strong>for</strong> processing<br />
microarrays used in new aCGH tests<br />
from Agilent, Roche/NimbleGen, Illumina,<br />
and others.<br />
SciGene<br />
Circle No. 367 in the Reader Service Card<br />
LIAISON® Treponema Assay<br />
Introducing the LIAISON Treponema Assay,<br />
the first fully-automated, FDA-cleared<br />
chemiluminescent immunoassay to aid in<br />
the diagnosis of syphilis infection. With<br />
high sensitivity, as well as excellent specificity,<br />
the LIAISON Treponema Assay is used as a<br />
clinical lab screening or confirmatory test. Its<br />
ability to detect both IgM and IgG antibodies<br />
to Treponema pallidum ensures improved<br />
sensitivity in the diagnosis of early syphilis<br />
infections, compared with RPR and EIA<br />
methods. The use of recombinant antigens<br />
limits cross reactivity and provides superior<br />
specificity. Labs benefit from the excellent<br />
throughput of 180 results per hour and the<br />
total walk-away system.<br />
DiaSorin<br />
Circle No. 368 in the Reader Service Card<br />
LIAISON® Borrelia burgdorferi Assay<br />
The LIAISON Borrelia burgdorferi assay<br />
is the only fully-automated, FDA-cleared,<br />
chemiluminescent immunoassay available<br />
<strong>for</strong> Lyme disease serology. The use of the<br />
VlsE recombinant antigen provides the LIAI-<br />
SON Borrelia burgdorferi assay with superior<br />
specificity, reducing the diagnostic time and<br />
cost. The truly reactive samples are identified<br />
in the first step of the recommended testing<br />
algorithm, reducing the amount of subsequent<br />
Western blot testing. Thanks to the<br />
high immunogenicity of the VlsE antigen,<br />
Lyme infections can be identified from the<br />
early stages and treatment can be started<br />
promptly. The LIAISON Borrelia burgdorferi<br />
assay has excellent throughput and random<br />
access capability.<br />
DiaSorin<br />
Circle No. 369 in the Reader Service Card<br />
LIAISON® 25 OH Vitamin TOTAL-DTM Assay<br />
The LIAISON 25 OH Vitamin TOTAL-DTM<br />
Assay uses chemiluminescent immunoassay<br />
technology <strong>for</strong> the quantitative determination<br />
of 25-hydroxyvitamin D and other hydroxylated<br />
vitamin D metabolites in human<br />
serum, EDTA-plasma, or lithium-heparin<br />
plasma <strong>for</strong> assessment of Vitamin D sufficiency.<br />
The new TOTAL-D is the only FDAcleared,<br />
fully-automated assay measuring<br />
100% of Vitamin D2 and D3. The improved<br />
precision offers intra and inter CV of ≤ 10%<br />
and functional sensitivity of < 4 ng/mL. The<br />
automated LIAISON Analyzer offers the lab<br />
a throughput of 100 tests per hour and time<br />
to first result of 35 minutes.<br />
DiaSorin<br />
Circle No. 370 in the Reader Service Card