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* 1. How important is wide dynamic range (6-7 logs) for your experiments?

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* 2. Which segment of assay dynamic range is most important for your work?

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* 3. Do you run multiplex assays on samples that could have a wide range of concentrations between the various included analytes? (> 4 logs apart)?

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* 4. How important is absolute quantitation - as compared to relative quantitation - for your experiments?

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* 5. What level of sensitivity do you require for your immunoassays?

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* 6. What is your requirement for inter-assay CVs? (different consumable runs)

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* 7. What is your requirement for intra-assay CVs? (within the same consumable run)

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* 8. What is the maximum assay run time that would be acceptable for your applications?

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* 9. What level of multiplexing do you typically require for biomarker discovery assays?

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* 10. What level of multiplexing do you typically require for validation assays for key biomarkers?

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* 11. Do you run multiplexed diagnostic assays?

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