Beckman Coulter, Inc.
 Contact Information: 4300 N. Harbor Boulevard
P.O. Box 3100
Fullerton CA 92834-3100
United States
800-742-2345

 Company Type:

Private
 Company Description: Beckman Coulter, Inc. is a leading manufacturer of biomedical testing instrument systems, tests and supplies that simplify and automate laboratory processes. Spanning the biomedical testing continuum—from pioneering medical research and clinical trials to laboratory diagnostics and point-of-care testing—Beckman Coulter's 200,000 installed systems provide essential biomedical information to enhance health care around the world. The company, based in Fullerton, Calif., reported 2007 annual sales of $2.76 billion with more than 78 percent of this amount generated by recurring revenue from supplies, test kits and services.

 
 Website: http://www.beckmancoulter.com
 
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    Product Literature
ICON® Mono Product Literature
When your patients present with fever, sore throat, swollen lymph glands or other symptoms common with a viral infection, you may not be able to distinguish these from infectious mononucleosis (IM). ICON® Mono is the one-step antibody test for fast, accurate, and easy-to-read results at the point-of-care. Product Features • Combines finger-stick whole blood convenience with EIA membrane technology for fast, accurate results. • Uses direct solid-phase immunoassay technology for early qualitativ

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TPOAb Access Assay Product Literature
• Quantitative method aids in the diagnosis of autoimmune thyroid disease in human serum or plasma • Utilizes recombinant human TPO to eliminate contamination from other thyroid antigens • Standardized to WHO 66/387 international standard • Reference interval established following NACB guidelines • Small sample size (10 μL) • Broad dynamic range: 0.25 – 1000 IU/mL

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AFP 300 Access Assay Product Literature
• Analytical sensitivity of 0.5 ng/mL (0.41 IU/mL) • Calibration stability: 28 days • Excellent lot-to-lot, lab-to-lab performance • Seven-level AFP calibrators prepared gravimetrically from human AFP in buffered BSA matrix, recovers WHO 1st International Standard, 72/225 target level • To aid in the detection of fetal open neural tube defects (ONTD) and for the measurement of AFP in the management of nonseminomatous testicular cancer • Automated on-line dilution extends measurable range to appr

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DHEA-S Access Assay Product Literature
• For the quantitative determination of DHEA-S in serum or plasma • Analytical sensitivity: 2 μg/dL • Broad dynamic range: 2 – 1000 μg/dL • Calibration stability: 28 days • Imprecision: 10 percentage CV @ ≥20 μg/dL

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• IgM immunocapture assay - Early detection of seroconversions - No competition with specific IgG - No interference with rheumatoid factor • Ready-to-use reagents, including the conjugate

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• To aid in the management of breast cancer patients • For the quantitative determination of CA 15-3 antigen levels in human serum and plasma using the Access® Family of Immunoassay Systems • Access chemiluminescent technology delivers highly specific and sensitive performance • Upper reference limit for apparently healthy females: 31.3 U/mL • Broad dynamic range: 0.5 - 1,000 U/mL • No hook effect up to 30,000 U/mL • Open Pack Stability: 56 days • Calibration Stability: 56 days

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CEA Access Assay Product Literature
• One step dual monoclonal antibody assay • Broad dynamic range up to 1000 ng/mL • No hook effect up to 100,000 ng/mL • Time to first result: 15 minutes • Calibration curve stability: 28 days

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• Quantitative chemiluminescent assay • Aids in diagnosis of myocardial infarction • Expected Value: or equal to 4.0 ng/mL • Time to first result: 15 minutes Calibration stability: 28 days

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Cortisol Access Assay Product Literature
• Quantitative determination of cortisol levels in serum and urine • Cross-reactivity with dexamethasone: 0.2 percentage (suppression test) • Time to first result: 30 minutes

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Rubella IgG Access Assay Product Literature
• Highly specific and sensitive • Immunity threshold: 15 IU/Ml • Reportable range of up to 500 IU/mL • Standardized against the WHO Reference Preparation (2nd I.S.P.) • Calibration stability: 28 days • Two level QC controls • Time to first results: 35 minutes

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Gastroccult® Product Literature
Gastroccult is the only test designed specifically for detecting gastric occult blood and determining gastric pH. It includes a convenient pH comparison chart for the Clinically relevant range which is important in monitoring antacid prophylaxis. With Gastroccult, medical personnel can now spend less time testing gastric samples for occult blood and pH.

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For thirty years, the Hemoccult® fecal occult blood test (FOBT) has been aiding physicians in detecting hidden blood in stool specimens as an early indication of colorectal cancer. More than 300 studies using Hemoccult® products – many of which were conducted over long periods of time with large numbers of participants- have been published in leading medical journals around the world. As a result of these studies, the American Cancer Society and other healthcare and medical agencies now recommen

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Hemoccult® ICT is the latest and most advanced fecal occult blood test (FOBT) in the Hemoccult product line. An immunochemical FOBT (iFOBT) with high specificity and sensitivity, Hemoccult ICT is clinically proven to detect bleeding associated with more cancers and polyps than traditional guaiac-based FOBTs. Because of its superior specificity for lower GI bleeding, Hemoccult ICT is an ideal screening tool for colorectal cancer (CRC), and this specificity also reduces the number of false positiv

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Hemoccult SENSA fecal occult blood tests have been used with confidence in medical practice as a way to enhance detection of hidden blood in stool specimens, an early indication of colorectal cancer. Many recent studies show that annual screening with Hemoccult® will reduce mortality from colorectal cancer by 20 to 40 percent.

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Hemoccult II SENSA elite Product Literature
Hemoccult II SENSA elite was designed to improve patient compliance. Its simplified test card, clearer patient instructions, and sample collection options make this fecal occult blood test easier for patients to understand and complete. Diet guidelines are explained in an easy-to-read format to help patients determine which foods and drugs are okay and which should be avoided during the testing period. The single back flap and Performance Monitor make processing and interpreting the elite test e

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ProteomeLab™ IgY -- Plasma/Serum Proteome Partitioning Solutions Product Literature
Biomarker discovery is like panning for gold. Finding the nuggets gets easier when there is less sand. Within biofluid proteomes such as plasma and serum, that "sand" is comprised of well-characterized proteins. Identifying the potentially golden biomarkers in the presence of these highly abundant proteins has proven to be a serious challenge to current analytical techniques. In serum and plasma, the dynamic range of proteins spans over 10 orders or magnitude, far greater than the measurement c

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ProteomeLab™ IgY-12 High Capacity Primate-Optimized Proteome Partitioning Kits Product Literature
ProteomeLab IgY-12 High Capacity Primate-Optimized Proteome Partitioning Kits Enrich Low Abundance Protein-based Biomarkers up to 25 times. The ProteomeLab IgY-12 High Capacity Proteome Partitioning kits are specifically designed to remove twelve highly abundant proteins from human/primate biological fluids such as serum and plasma. This provides an enriched pool of lower abundant proteins, free from interference by the removed proteins, ready for discovery and validation of biomarkers, drug

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ProteomeLab™ IgY-R7 Rodent-Optimized Proteome Partitioning Kits Product Literature
The ProteomeLab IgY-R7 Proteome Partitioning kits are specifically designed to remove seven highly abundant proteins from rodent biological fluids such as serum and plasma. This provides an enriched pool of lower abundant proteins, free from interference by the abundant proteins, ready for discovery and validation of biomarkers, drug targets, and therapeutic proteins and antibodies. Kits are available in both spin column and LC column formats, depending upon the desired capacity per cycle. The

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ProteomeLab™ IgY Single-Component Proteome Partitioning Kits Product Literature
The ProteomeLab IgY Proteome Partitioning Spin Column kits are based on affinity columns using avian antibody (IgY)-antigen interactions and optimized buffers for sample loading, washing, eluting and regenerating. They are designed to work with the ProteomeLab SP sample preparation system and specifically remove a targeted protein from biological fluids such as serum, plasma, and cerebral spinal fluid (CSF) so as to enhance discovery and validation of biomarkers, drug targets, and therapeutic pr

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Phenobarbital is a long-acting barbiturate used to control convulsions caused by tonic-clonic (grand mal), focal or psychomotor epileptic seizures. It has been used for anxiety, insomnia and gall bladder dysfunction or blockage. It is the drug of choice for treatment of febrile seizures and neonatal seizures in infants born to opiate- or barbiturate-addicted mothers. Additionally, it has been used prenatally and postnatally to prevent and treat hyperbilirubinemia (familial non-hemolytic, non-obs

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Access® Digoxin Product Literature
• Dynamic range: 0.2-6.0 ng/mL • Therapeutic range: 1-2 ng/mL • Reproducibility: CV or equal to 10 percentage • Time to first result: 20 minutes • Cross-reactivity with digitoxin: 2.9 percentage

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Access® Digoxin Calibrators Product Literature
• Dynamic range: 0.2-6.0 ng/mL • Therapeutic range: 1-2 ng/mL • Reproducibility: CV or equal to 10 percentage • Time to first result: 20 minutes • Cross-reactivity with digitoxin: 2.9 percentage

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Access® Digoxin Zero Calibrator Product Literature
• Dynamic range: 0.2-6.0 ng/mL • Therapeutic range: 1-2 ng/mL • Reproducibility: CV or equal to 10 percentage • Time to first result: 20 minutes • Cross-reactivity with digitoxin: 2.9 percentage

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ICON® 20 hCG Product Literature
Finally, there’s an easy-to-use hCG urine/serum combo test that you can rely on for more sensitivity, higher accuracy, and faster results at the point-of-care – ICON® 20 hCG from Beckman Coulter. ICON 20 hCG is a rapid test for detecting hCG qualitatively, employing a solid-phase chromatographic immunoassay technology to selectively detect elevated levels of hCG in serum or urine.

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ICON® DS Strep A Product Literature
ICON DS Strep A is a rapid immunochromatographic assay for the qualitative detection of Group A Strep antigen directly from a throat swab specimen. ICON DS Strep A is a simple, easy-to-use CLIA-waived dipstick format test. With outstanding performance, even in low colony count samples, ICON DS Strep A leaves little chance for misdiagnosis, minimizing the chance of rheumatic fever or over-prescription of antibiotics. In as little as five minutes, you will have accurate results so you can begin y

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ICON® SC Strep A Product Literature
ICON SC Strep A, the new and improved rapid test from Beckman Coulter Primary Care Diagnostics, is reliable, affordable and easy to use. ICON SC Strep A is a simple, easy to use CLIA-waived test. No mixing, no measuring and no fragile trays. The easy-to-handle cassette format with clearly visible result window makes test results simple to interpret. In as little as five minutes, you will have accurate results so you can begin your patient’s treatment immediately and confidently.

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Phosphorus (PHS) Product Literature
Beckman Coulter’s Phosphorus (PHS) reagent is a random access assay that provides the advantage of automatic on-line urine sample dilution (1:10) on the UniCel® DxC and SYNCHRON CX® PRO and SYNCHRON LX® systems.

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UniCel® DxC 600 Synchron® Clinical System Product Literature
UniCel DxC systems are built to deliver maximum productivity for your laboratory. The systems have the capacity to help your lab thrive in today’s environment. Plus, designed to minimize workflow interruptions and maximize ‘user-friendliness’, the UniCel DxC systems deliver a faster, reliable turnaround time.

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