The liquid stable,
ready-to-use MATRIX PLUS™ Chemistry Reference
Kit is now available from VERICHEM
LABORATORIES. Intended for the calibration, or
calibration verification, of wet chemistry assays on clinical testing systems,
the kit is designed to meet the needs of a wide variety of clinical laboratory
professionals, as the materials are expressly designed to support overall
system QC and CLIA
compliance. This product is a valuable tool in determining a clinical system’s bias
to the true, or known, value. By maintaining a constant
protein content and neutral pH across concentration levels, the unique
formulation and CLSI EP06-A set point design of these reference materials are
crucial for the independent determination of test method accuracy, sensitivity,
linearity and reportable range.
In conjunction with
the optional sixth Level F, this set of definitive method reference material
contains seven (7) routine chemistry components, covering forty-two (42)
individual concentrations. Analytes include Blood Urea Nitrogen (BUN), Calcium,
Creatinine, Glucose, Magnesium, Phosphorus, and Triglyceride. The materials are
intended to be treated as patient specimens with wet clinical testing systems
and suitable for a wide variety of testing methods, including visible spectrum,
ultraviolet, kinetic, and/or endpoint.
Verichem
LABORATORIES’
MATRIX PLUS™ Chemistry Reference
Kit is packaged in ready-to-use, liquid stable format, incorporating a buffered
protein based matrix for serum-like reactivity. Formulation features
undetectable lot-to-lot variation, and is free of glycols, surfactants, azide and
other interfering substances. Each active component is verified using available
Standard Reference Materials from the National
Institute of Standards and Technology (NIST) and documented with a Certificate of Analysis. In
addition, Verichem
LABORATORIES’MATRIX PLUS™ Chemistry Reference
Kit offers exceptional open-vial product stability claims of twenty-one (21)
months.
VERICHEM LABORATORIES serves the clinical
laboratory testing and in-vitro diagnostic (IVD) manufacturing markets with a
comprehensive line of calibration, verification products, chemistry standards,
reference materials, and support services, including free, instant online data
reduction reports for CLIA compliance. For additional information, contact
Verichem Laboratories Inc. at 90 Narragansett Avenue, Providence, RI 02907
USA. Phone: 800-552-5859; FAX: 401-467-1540; Email: customerservice@verichemlabs.com.
Please visit our website at www.verichemlabs.com.