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Description
Samples have been selected to demonstrate IgG and/or IgM reactivity; in addition, one negative serum and three negative plasmas have been included as nonreactive controls
- For research use only
- Extensive array of panels helps labs maintain the highest standards for assay validation, regulatory compliance and method development
- Each panel includes comprehensive, comparative data from a variety of methods and commercially available test kits, allowing reagent assay/platform performance, sensitivity and specificity to be independently challenged
- Assembled from highly characterized, disease state patient samples, and developed specifically for infectious disease testing
- Enables labs to evaluate, monitor and troubleshoot test and staff performance
- Minimizes down time and accelerates validation and verification of new test methods, reagent systems and platforms
- SeraCare panels are rigorously tested and characterized using the highest quality test methods
- Comprehensive test results provided with each panel; quantified against international standards when available
- Long-term stability and availability
- All SeraCare facilities are ISO 9001 and 13485 certified and comply with cGMP standards
Specifications
Specifications
| Certifications/Compliance | ISO 9000 13485 |
| Content And Storage | Frozen |
| Format | Panel |
| Type | Anti-EBV Mixed Titer Performance Panel |
| Includes | Set of 25 members: 21 members with Infectious Mononucleosis heterophile antibody and/or EBV specific reactivity, one negative Serum and three negative Plasmas as nonreactive controls |
| Intended Use | Evaluating infectious Mononucleosis heterophile and Epstein Barr Virus specific Antibody tests with characterized samples, to provide comprehensive data for comparative analysis |
| Matrix | Serum and Plasma |
| Quantity | 25 x 0.5 mL |
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