Home / Clinical Laboratory / Clinical Analyzer Calibrators and Reagents / Reagents / Reagent Kit / Reagent Kit QMS® Therapeutic Drug Monitoring Amikacin For Automated Clinical Chemistry Analyzers 172 Tests R1: 2 X 18 mL, R2: 2 X 9 mL373910
Picture of Reagent Kit QMS® Therapeutic Drug Monitoring Amikacin For Automated Clinical Chemistry Analyzers 172 Tests R1: 2 X 18 mL, R2: 2 X 9 mL373910

Reagent Kit QMS® Therapeutic Drug Monitoring Amikacin For Automated Clinical Chemistry Analyzers 172 Tests R1: 2 X 18 mL, R2: 2 X 9 mL373910

Reagent-Kit-QMS®-Therapeutic-Drug-Monitoring-Amikacin-For-Automated-Clinical-Chemistry-Analyzers-172-Tests-R1:-2-X-18-mL,-R2:-2-X-9-mL373910

SKU #

#1100649

MPN #

373910

Brand

Ortho Clinical Diagnostics

Stock

In Stock

Quantity

100

Features

REAGENT, AMIKACIN (172TEST/BX)D/S

$929.70 USD

Product Specifications Product Usage Additional Information
Print
Attribute Name Attribute Value
McKesson # 1100649
Manufacturer # 373910
Brand QMS®
Manufacturer Ortho Clinical Diagnostics
Application Reagent Kit
Container Type Bottle
For Use With For Automated Clinical Chemistry Analyzers
Form Ready-to-Use Liquid
Number of Tests 172 Tests
Product Dating McKesson Acceptable Dating: we will ship >= 60 days
Sample Type Human Serum / Plasma Sample
Storage Requirements Requires Refrigeration
Test Name Amikacin
Test Type Therapeutic Drug Monitoring
Type Particle-Enhanced Turbidimetric Immunoassay
UNSPSC Code 41116007
Volume R1: 2 X 18 mL, R2: 2 X 9 mL
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  • The QMS Amikacin assay is intended for the quantitative determination of amikacin in human serum or plasma on automated clinical chemistry analyzers
  • 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