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Clinical Laboratory News - American Association for Clinical ...

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special section<br />

Advertisement<br />

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

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