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SEQme was established in 2012 to provide full solutions in the field of
DNA sequencing and Real-Time PCR.
We conduct sample analyses, organize courses and workshops
focused on these techniques and provide instrument services.
More about us
In the first part we discussed how to troubleshoot no or low signals. Basically empty electropherograms. Very frustrating. Now, I focus on another frequent result – you obtain some signals but the height of the DNA sequencing peaks diminished rapidly. A…
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When sequencing PCR products, the fluorescent signal sometimes drops sharply and the PCR product sequence is not read completely. A typical cause of this problem is the presence of various inhibitors in templates of sequencing reactions.
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