About Us
Technology
Technology
In real-time PCR, detection performance depends on how precisely fluorescent signals can be separated from background noise. TetraWare™ Detachable Well Plates feature a proprietary plastic surface treatment that raises fluorescence detection sensitivity and signal-to-noise ratio (SNR). The result is sharper signals and lower background, even with the same detection kit.
Thanks to the detachable design, plates separate into 8-well strips, so you can run anywhere from 8 to 96 wells to match your sample count. One product covers everything from small studies to large-scale screening — with less waste.
Instrument : BIO-RAD CFX96™
Instrument : Thermo Fisher QuantStudio™ 5
Extraction Formulations for Diverse Sample Types
Tetra Biotech has developed proprietary formulations for extracting and purifying high-purity nucleic acids from a wide range of clinical and research samples, including blood, swabs and tissue. By effectively removing PCR inhibitors, they deliver high purity (A260/280 ≥ 1.8) and consistent yields.
Our portfolio includes manual kits for hands-on bench work and automation kits compatible with leading nucleic acid extraction systems. The automation kits are validated across platforms to deliver consistent performance in high-throughput settings.
Sample-Specific Extraction
Optimized formulations for blood, swabs, tissue and more deliver high extraction efficiency.
High Purity, Reliable Results
Effective removal of PCR inhibitors improves the accuracy of downstream PCR/RT-PCR analysis.
Flexible, Scalable Workflows
From manual to automated kits, seamlessly paired with our PCR reagents for a faster workflow.
Next-Generation Taq Polymerase, Engineered with SGME
TetraZyme™ was developed on our SGME platform, which uses AI-driven structural analysis to pinpoint key amino acid residues around the active site of Taq polymerase and introduce optimized mutations at those positions. The key breakthrough: overcoming, at the structural level, the unstable dNTP binding and limited amplification efficiency of wild-type Taq polymerase.
Minimal non-specific amplification, even with complex samples and GC-rich targets
Lot-to-lot consistency proven in research and clinical diagnostic settings
Enhanced dNTP Binding
Optimized dNTP binding efficiency and Mg²⁺-dependent kinetics accelerate polymerization.
Reduced Primer Dissociation
Lower primer dissociation keeps amplification efficiency stable across more cycles.
Extended Exponential Phase
Delaying the plateau extends the exponential phase, improving quantitative accuracy and reproducibility.
PCR Assay Design, Powered by TetraZyme™
Built on our in-house TetraZyme™ enzyme platform, Tetra Biotech designs PCR assays that deliver outstanding detection performance. Because we control enzyme performance in-house, we can optimize the sensitivity and specificity of every detection kit from the very first design stage.
For primer and probe design, we use AI-based oligonucleotide design tools. By evaluating target specificity, secondary structure, GC content and dimer-formation potential, they rapidly and accurately identify the optimal sequences for maximum amplification efficiency and specificity.
This combination of high-performance TetraZyme™ enzymes and AI-driven oligo design feeds directly into our OEM/ODM services. We design detection assays around each partner’s targets and specifications, pair them with optimized TetraZyme™ master mixes, and deliver refined molecular diagnostic products on accelerated timelines.
Built on TetraZyme™
By controlling detection performance end to end with our own enzyme, we ensure consistent quality without depending on external raw materials.
AI-Driven Oligo Design
AI-optimized primers and probes deliver robust detection even for challenging targets while shortening development time.