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What is the best way to purify PCR products?

For most applications, it is best to purify PCR products by gel electrophoresis.

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Why do I receive less than the requested scale quantity for a synthesized oligonucleotide?

The scale of the oligonucleotide synthesis reaction is based solely on the starting material. As no chemical reaction is 100% efficient, the final deliverable amount is never equal to the starting amount for synthesis.

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Are there any special requirements for the handling and storage of my labeled probes?

Labeled probes should, for the most part, be handled in the same fashion as other custom oligonucleotide sequences. We recommend resuspending probes in TE buffer.

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