Primer Design*
| Erwin van Rijn |
|---|
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Call: +31 (0)71 523 3917 |
| Contact us |
Avoid Hairpin loop, dimers and false priming: optimised DNA sequence |
Optimised Tm and GC content |
In-house oligosynthesis: No data leaves BaseClear; confidentiality guaranteed! |
Special oligosynthesis programs can be made on request for high oligo quality. |
40 nmol or 200 nmol oligo scale |
Desalted or reverse phase chromatography (alternative for HPLC purification; same quality, half price) |
Oligonucleotide design and synthesis*
Hairpin loops, (cross-) dimers and false priming are a couple of factors that will determine the efficiency of your oligo in a PCR/sequence reaction. With this service we will design oligonucleotides and avoid such factors for you. Other factor as Tm and GC contents can be adjusted to customers wishes. Provides us with the target sequence and the range in which primer(s) should be design and we will provided you with the best possible primer design. As off 1-9-2005 we will have in house oligosynthesis, after that date no data leaves BaseClear and is confidentiality guaranteed! All oligonucleotide come as desalted freeze-dried, complete with a report. As extra service and for oligonucleotides >30-40 mer, oligonucleotides can be purified with reverse phase chromatography (90% pure full-length oligo).
Digital form of the target DNA and the range in which the primer(s) should be designed.
| Please contact us for more information |
* This service can only be offered in combination with sequencing orders.

