About this item
The AriaMx Real-time PCR System is a fully integrated quantitative PCR amplification, detection, and data analysis system.
- Gene expression analysis
- New genotyping/HRM capability, mRNA quantification
- NGS quantification: library preparation, result validation, nucleic acid monitoring, rare allele detection
- Can use self-Installable optical cartridges
- Operates at a Cq uniformity standard deviation of <0.20 at fast cycling (5 sec at 95 °C / 10 sec at 60 °C)
- Data acquisition time of <3 sec/plate
- Dynamic range of 9 orders of magnitude
- Operates at a maximum altitude of 2000 m and in 20 to 80% relative humidity
The system design combines a state-of-the-art thermal cycler, an advanced optical system with an LED excitation source, and complete data analysis software.
This instrument can hold up to six optics modules, and the scanning optics design delivers optimal separation between the dyes and between samples and provides a closed-tube PCR detection format that can be used with a variety of fluorescence detection chemistries including SYBR® Green and EvaGreen dyes as well as fluorogenic probe systems including TaqMan probes.
The AriaMx amplifies the productivity with its unique modular and flexible design, intuitive touch-screen interface, advanced, easy-to-use reporting and 120+ attributes monitored through the built-in on-board diagnostics to help pinpoint assay or instrument issues as they arise.
Includes configurable optical modules(up to 6), a touchscreen controller, Experimental Import, LIMS connectivity, 96 wells, 5GB of protocol storage, on-baord instrument diagnostics, remote monitoring capabilities, one year standard warranty.
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- • State issued document with your organization's Federal Tax ID Number
- • State issued document with your organization's Resale Tax ID Number
- • City or County issued Business License
- • State Department of Health Services License
- • Any other ID issued by the State that includes the business name & address
* ATTN: California Customers may require additional documentation as part of the CA Health & Safety Code. Products that fall under this regulation will be placed on a mandatory 21-day hold after documentation is received. Avantor will not lift restrictions for residential shipping addresses.