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Pcr Software
Reference: 945765Laboratory Medicine
| Applications | For Pcr, Laboratory |
| Function | Import, Interpretation |
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Product information
Product summary
The interpretation of the results obtained with RealType products for the study of point mutations through genotyping tests by Real-time PCR is facilitated by the BioVisor RT software.input:
output:BioVisor RT imports the fluorescence data from the PCR equipment in real time, analyzes it automatically, and generates a report containing the results.input:
output:The application has been validated for the CFX96 (Bio-Rad), ABI7500 (Life Technologies), and MIC (Biomolecular Systems) instruments.input:
output:
Management of users and permissions
Genotyping determination that is automated
Importation of data from the PCR instrument
interpretation of each sample's findingsinput:
output:Interpretation of the series in accordance with the results of the controls
The publication of a results report
Compatibility with the most frequently employed real-time PCR instrument
The work series file
output:BioVisor RT imports the fluorescence data from the PCR equipment in real time, analyzes it automatically, and generates a report containing the results.input:
output:The application has been validated for the CFX96 (Bio-Rad), ABI7500 (Life Technologies), and MIC (Biomolecular Systems) instruments.input:
output:
Management of users and permissions
Genotyping determination that is automated
Importation of data from the PCR instrument
interpretation of each sample's findingsinput:
output:Interpretation of the series in accordance with the results of the controls
The publication of a results report
Compatibility with the most frequently employed real-time PCR instrument
The work series file
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The support team can coordinate delivery options by destination, product type, and documentation requirements before confirming availability.
Are fragile or calibrated products handled differently?
Sensitive products are packed with additional cushioning and handling notes; calibration or compliance documents can be reviewed during the inquiry process.
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Lead time depends on stock status, destination, carrier availability, and any requested documentation. Contact the product team for a product-specific estimate.
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