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• 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
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Company:
Date:
December 15, 2008
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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
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Company:
Date:
December 15, 2008
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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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Company:
Date:
December 15, 2008
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Monoclonal anti-LPS antibody , Time to first result: 30 minutes (after extraction) ,Simple chemical extraction , Fully-automated blocking assay (included) , 24-hour calibration stabiity , Low-positive QC control
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Company:
Date:
December 15, 2008
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Quantitative chemiluminescent assay, Aids in diagnosis of myocardial infarction, Expected Value: ² 4.0 ng/mL ,Time to first result: 15 minutes
,Calibration stability: 28 days
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Company:
Date:
December 15, 2008
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Quantitative determination of cortisol levels in serum and urine ,Cross-reactivity with dexamethasone: 0.2 (suppression test) ,Time to first result: 30 minutes
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Company:
Date:
December 15, 2008
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• 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 CV @ ≥ 20 μg/dL
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Company:
Date:
December 15, 2008
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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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Company:
Date:
December 15, 2008
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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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Company:
Date:
December 15, 2008
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• 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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Company:
Date:
December 15, 2008
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