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qPCR FAQs

Q:What is the function of Passive Reference Dye and how to use it?

A:

They are reference fluorescent dyes used to normalize pipetting errors compatible with different instruments. Their concentration is provided at 50 ×, and 0.4 μl is needed for 20 µl reaction.


Q:Why do CT values appear too late?

A:

It may be because the amplification efficiency is low due to the non-optimal reaction conditions. The degradation of PCR reaction components or too big size of PCR products (typically PCR products of 80-250 bp are required) could also cause late CT.


Q: Does Mg2+ concentration need to be adjusted in qPCR SuperMix?

A:

Generally, it doesn’t need adjustment, but when the PCR results are not optimal or other adjustments cannot lead to significant improvement, amplification results can be improved by adjusting Mg2+ concentration.


Q:Why is the amplification curve abnormal?

A:

· The baseline setting is incorrect.

· High concentration of templates can cause low CT value, i.e. the baseline range becomes smaller, resulting in an incorrect reading of fluorescent values by the instrument.


Q: Why is the repeatability poor?

A:

· Operative errors.

· Low template concentration can lead to poor repeatability. It is recommended to increase template concentration or decrease the dilution fold.

· Temperatures between different wells of the instrument are not consistent.


Q:NTC is not zero, and how to optimize it?

A:

· Increase the annealing temperature.

· Reduce the working concentration of the primer.  If necessary, the concentration can be reduced to 60 nM.

· It is recommended to operate on ice.

· Redesign the primer. If necessary, design multiple primers and choose the best one.