Oligonucleotide Synthesis

Custom Oligonucleotides for Reliable Performance

We synthesize high-quality DNA oligonucleotides (primers) tailored for a wide spectrum of molecular biology applications. Our primers deliver precise target recognition, efficient hybridization, and reliable amplification performance across PCR, qPCR, genotyping, sequencing, and mutagenesis assays. Our portfolio includes standard DNA primers, LNA-modified primers, phosphorothioate-modified primers, and primers with various terminal modifications.

Note: Terminally modified primers (biotin, thiol, digoxigenin, phosphorylation, Tamra, azide, alkyne, and internal spacer) are available through our TaqMan® Probe Order Page.

Production & Quality Assurance

Each primer is synthesized using high-purity reagents under stringent contamination-free conditions, ensuring optimal coupling efficiency and sequence fidelity. All oligonucleotides undergo rigorous quality control, including LC-MS and spectrophotometric analysis to assess sequence accuracy, purity, and concentration.

Lyophilized primers maintain stability for up to 1 year at +4°C. Once reconstituted in nuclease-free water or TE buffer, primers remain stable for up to 6 months at -20°C, depending on buffer composition and pH.

Purification Guidance

We offer multiple purification options to suit diverse experimental needs. Choose the method that best matches your application to ensure optimal performance and reliability.

Desalt: Suitable for routine PCR and standard applications

OPC/RPC: Optimal for applications requiring higher purity and minimal byproducts

HPLC: Recommended for sensitive downstream applications such as cloning, sequencing, or mutational analysis

Delivery Stage

  • Orders shipped within 1–3 business days
  • Primers are delivered lyophilized in vacuum-sealed, moisture-protected tube
  • The product is accompanied by a detailed guide containing sequence information, purification method, and absorbance data (A260, OD, nmol, etc.).
Key Features

Key Features

Custom synthesis from 20 to 150 bases
Multiple purification options
Minimal secondary structure formation
High sequence fidelity and consistent amplification efficiency
Contamination-free and nuclease-free production environment
Lyophilized format for long-term stability
Common Applications

Common Applications

PCR and qPCR amplification
DNA cloning and sequencing primers
Genotyping and SNP analysis
Mutation detection assays
Primer-based hybridization assays
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