MD3850_OncoMate-5C-Matrix-Standard_3

  • 5C Matrix Standard labeled with fluorescein, JOE, TMR-ET, CXR-ET and WEN
  • Calibration Standard for use with the OncoMate® MSI Dx Analysis System
  • IVD Medical Device
  • CE-Marked and available in select European countries; FDA-cleared in the United States

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Catalog Number: MD3850

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Overview
Protocols
Specifications
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The OncoMate® 5C Matrix Standard consists of DNA fragments labeled with five different fluorescent dyes (fluorescein, JOE, TMR-ET, CXR-ET and WEN) in one tube. The spectral calibration is performed according to the instrument manufacturer's instructions. OncoMate® 5C Matrix Standard is used to calibrate capillary electrophoresis instruments prior to running the OncoMate® MSI Dx Analysis System to distinguish fluorescent signals from the specific dyes used in the assay.

Intended Use statement: The OncoMate® 5C Matrix Standard is intended for in vitro diagnostic use as an IVD medical device accessory used with the OncoMate® MSI Dx Analysis System (Cat.# MD3140). The standard is used for spectral calibration of capillary electrophoresis instruments prior to analysis of amplification products generated with the OncoMate® MSI Dx Analysis System. This product is intended for professional use only.

Representative Data

Figure 16091MA - Representative data for the OncoMate™ 5C Matrix Standard
Figure 1. OncoMate® 5C Matrix Standard data. Panel A. Resolved fragment peaks. Panel B. Dye emission spectra.

Specifications

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Lieferumfang

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Matrix Dilution Buffer

MD191A 5 × 200μl

5C Matrix Mix

MD430A 1 × 150μl

Analysezertifikat

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Nutzungseinschränkung

For In Vitro Diagnostic Use. This product is only available in certain countries.

Lagerhinweise

BB

Patente und Haftungsausschlüsse

U.S. Pat. No. 9,139,868, European Pat. No. 2972229, Japanese Pat. No. 6367307 and other patents pending.

Resources

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The OncoMate® 5C Matrix Standard (Cat.# MD3850) is available in the following countries: Austria, Belgium, Czech Republic, Denmark, France, Germany, Hungary, Ireland, Italy, Luxembourg, Netherlands, Norway, Poland, Romania, Slovakia, Spain, Sweden, Switzerland and the United Kingdom. For information about availability in other regions, including the FDA-cleared product in the United States, please contact us.