-
,for, Item ID-
- #1184752
- Microgenics #0373589
Immunoassay Reagent QMS® Vancomycin CLIA Non-Waived For Automated Clinical Chemistry Analyzers
REAGENT, QMS VANCO (1/KT) D/S
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Features
- The QMS® Vancomycin assay is intended for the quantitative determination of vancomycin in human serum or plasma on automated clinical chemistry analyzers; The results obtained are used in the diagnosis and treatment of vancomycin overdose and in monitoring levels of vancomycin to help ensure appropriate therapy
- Significantly reduces labor, time, and expense compared to HPLC or LCMS and other technologies
- Based on competitive inhibition immunoassay principle whereby free-drug in the sample competes for antibody binding sites with drug molecules coated onto uniform microparticles
- More …
Product Details Email
Product Specifications
| McKesson # | 1184752 |
|---|---|
| Manufacturer # | 0373589 |
| Brand | QMS® |
| Manufacturer | Microgenics |
| Country of Origin | Unknown |
| Application | Immunoassay Reagent |
| Buy American Act (BAA) Compliant | No |
| CLIA Classification | CLIA Non-Waived |
| CLIA Classified | CLIA Non-Waived |
| Container Type | Bottle |
| For Use With | For Automated Clinical Chemistry Analyzers |
| Form | Ready-to-Use Liquid |
| Product Dating | McKesson Acceptable Dating: we will ship >= 90 days |
| Sample Type | Serum / Plasma Sample |
| Specialty | Immunoassay |
| Storage Requirements | Requires Refrigeration |
| Test Category | Therapeutic Drug Monitoring |
| Test Method | Particle-enhanced Turbidimetric Immunoassay |
| Test Name | Vancomycin |
| Trade Agreement Act (TAA) Compliant | No |
| UNSPSC Code | 41116007 |
| Volume | R1: 22 mL, R2: 22 mL |
Features
- The QMS® Vancomycin assay is intended for the quantitative determination of vancomycin in human serum or plasma on automated clinical chemistry analyzers; The results obtained are used in the diagnosis and treatment of vancomycin overdose and in monitoring levels of vancomycin to help ensure appropriate therapy
- Significantly reduces labor, time, and expense compared to HPLC or LCMS and other technologies
- Based on competitive inhibition immunoassay principle whereby free-drug in the sample competes for antibody binding sites with drug molecules coated onto uniform microparticles
- Liquid stable and ready-to-use
- Applicable to general chemistry analyzers
- Validated parameters assure lab-to-lab reproducibility
- Excellent correlation to reference methods
- Optimal sensitivity, precision and dynamic range
- Low cross-reactivity with metabolites and commonly co-administered drugs
- Low interference from endogenous substances
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