Custom DNA Oligos
- Custom DNA oligo synthesis from 2 to 300 bases
- Your choice of plate, strip or tube for optimal flexibility
- Standard DNA oligos are shipped within 24 hours
- Purified & modified oligos within 4 business days
- Over 300 modifications available
Custom oligos quality standards
DNA synthesis has been our core product for over 20 years. All custom oligos are manufactured under ISO 9001 and ISO 13485 quality standards. These quality standards reflect good reliable and safe products as a result of stringent production and manufacturing procedures.
Oligonucleotides up to 300 bases are achieved with our B-pure Oligonucleotide Synthesis protocol. This protocol enables high quality long oligo synthesis at an affordable price. By using the B-pure protocol we can achieve a coupling efficiency >99,5%.
>More about long oligos and coupling efficiency
Oligonucleotides longer than 80 bases are synthesized automatically on this protocol. Additional quality control is performed on our state-of-the-art LC-MS system to guarantee highest quality and optimized functionality of the oligonucleotides.
Biolegio offers four different synthesis scales for DNA oligos: 10 nmol, 40 nmol, 200 nmol and 1000 nmol. For each synthesis scale there is a restriction regarding the length of the oligo.
10 nmol scale: 40 bases max. length
40 nmol scale: 150 bases max. length
200 nmol scale: 225 bases max. length
1000 nmol scale: 300 bases max. length
For non-labeled, non-HPLC/PAGE purified standard DNA oligos up to 30 bases we guarantee a minimum yield. However in many cases you will receive more than the guaranteed minimum!
10 nmol scale: 10 nmol min. yield
40 nmol scale: 20 nmol min. yield
200 nmol scale: 95 nmol min. yield
1000 nmol scale: 400 nmol min. yield
Biolegio has three synthesis protocols: 'Economy' , 'High Purity' and 'B-pure'. The used protocol depends on the length of the oligo. This means that the protocols have been optimized for certain oligo lengths.
- Economy protocol is used for oligos between 2 and 49 bases.
- High purity protocol is used for oligos between 49 and 79 bases.
- All DNA oligos longer than 80 bases are synthesized on our B-pure synthesis protocol.
Each protocol delivers the highest possible coupling efficiency for the specified range.
Your DNA oligo can be shipped dry or dissolved, annealed or mixed. Standard DNA oligos are delivered dissolved in a tube in a concentration of 100 pmol/μl.
- H2O buffer
- LoTE buffer
- TE buffer
All DNA oligos are synthesized under low salt conditions. This avoids the need for purification for most basic molecular biology applications. Additional purification is available for more sensitive applications. Furthermore, we recommend purification for oligos longer than 40 bases.
We offer three different forms of purification:
Reverse-Phase cartridge purification
Modifications can be incorporated either during (direct) or after (indirect) synthesis. You can choose from over 300 modifications. If your desired modification is not listed on our website, please contact us.
Use the standard code letters for mixed bases / wobbles.
DNA/RNA hybrid oligos can be ordered in with some minor adjustments in the sequence. Mark the RNA bases by placing a lower case 'r' in front of them. For DNA bases place a lower case 'd' in front. For 'chemistry' choose DNA/RNA hybrid.
Unmodified oligos can be used for at least 12 months when stored at -20°C. Use nuclease-free, sterile water for working solutions. Oligonucleotides modified with fluorescent dyes should be kept away from light as much as possible. Avoid repeated freeze-thaw cycles as this process can lead to degradation of the oligo.
All your DNA oligos are delivered with a specification sheet including GC-content, molecular weight, melting temperature (Tm), OD value, sequence and quantity in μgram and nmol.
A stringent quality control system ensures that you can expect the quality of our oligonucleotides to be of the highest standard. Before the synthesis, all chemicals are checked to meet our quality standards. During the fully automated oligo synthesis, all steps of the synthesis are monitored by multiple control functions on our DNA synthesizers. This way we can assure the coupling efficiency of the synthesis to meet our demands.
Synthesis is followed by further quality controls to guarantee the quality of the oligos. All oligos are routinely analyzed by optical density (OD) measurement. In addition, oligos are analyzed by gel electrophoresis and Liquid Chromatography Mass Spectrometry (LCMS). If oligos do not meet our requirement they are resynthesized. The result of our stringent QC process is a product of the highest standard. All oligos are delivered with our product specification sheet, which includes: % GC content, yield in nmol and μgram, OD, melting temperature and molecular weight (MW).
ISO quality management
ISO is an independent, non-governmental membership organisation and the worlds largest developer of voluntary international standards. Biolegio’s manufacturing facility is ISO 9001:2008 and ISO 13485:2003 certified. Achieving these certificates ensures good, reliable and safe products as a result of strong product quality and manufacturing procedures and an ongoing development of our quality management system. This ongoing development empowers us to continuously strengthen our ability to identify and exceed the needs and expectations of our customers.
Biolegio uses optimized phosphoramidite chemistry and reagents of the highest quality. Order handling and oligo synthesis programs result in an average coupling efficiency above 99,5%. With this efficiency we are able to synthesize DNA oligos up to 300 bases. Synthesis is performed under low salt conditions, which avoids the need for additional purification for most basic molecular biology applications, such as PCR, sequencing, hybridization studies and antisense studies. Additional purification by HPLC, PAGE or cartridge is available for more sensitive applications.
Oligonucleotide synthesis is carried out by a step-wise addition of nucleotide residues to the 5’-terminus of the growing chain until the desired sequence is assembled. Each addition is referred to as a synthetic cycle (figure 1) and consists of four chemical reactions: deblocking, coupling, capping and oxidation. At the end of the synthesis the oligo is released from the solid support and is eluted from the column or well. As solid support we use polystyrene beads (PB).