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FAQ - affigene® general

Q:

Can I use an affigene® trender kit as a qualitative test?

Q:

Why are there different values for the calibrators when using plasma or whole blood in affigene® CMV and EBV trender kit?

Q:

What is the Precision for affigene® trender assays?

Q:

What are the positive controls or high and low calibrators made from?

Q:

Against what quality controls or standards do you calibrate BKV kits?

Q:

Are there any toxic components in the affigene® trender-tracer kits?

Q:

What is a scorpion primer?

Q:

affigene HSV 1/2 utilizes CSF and swab samples for determination in real-time PCR
Is there a protocol that utilizes serum or plasma samples?

Q:

What is the quantitative range for HBV trender using serum samples?

Q:

Can I compare copies/mL and copies/100 000 cells?

Q:

Which part of the EBV genome is amplified?

Q:

What is a positive sample?

Q:

What is the difference between linear range, dynamic range and quantitative range?

Q:

What is limit of detection (LOD)?

Q:

What is precision?

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What is accuracy?

Q:

What is Quantitative range?

Q:

What is Linearity/ linear range?

Q:

What is Dynamic range?

Q:

Are your products CE-labelled?

Q:

Do you have a license for PCR?

Q:

Is the CE-label valid when using a non-CE labelled PCR machine?

Q:

The sample titer obtained with affigene® trender does not correspond to results obtained using my previous protocol?

Q:

How can I compare my results with results from another laboratory?

Q:

Are two calibrators enough to give a reliable sample titer?

Q:

Is the test able to monitor only EBV reactivations or primary infections?

Q:

Is it possible to use urine-samples in affigene® CMV trender kit?

Q:

Which part of the CMV genome is amplified?

Q:

How can I be sure to pick up different variants of CMV?

Q:

What is the IC (internal control) manufactured from?

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