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- Products
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- Nucleic Acid Related
- Enzymes
- About
- About SBS
- Achievements
- Legal Statement
from China, for the World
for Superior Biology Services since 2000
- Products
- All Products
- Custom Services
- Catalog Products
- Innovative Systems
- Nucleic Acid Related
- Enzymes
- About
- About SBS
- Achievements
- Legal Statement
- …
- Products
- All Products
- Custom Services
- Catalog Products
- Innovative Systems
- Nucleic Acid Related
- Enzymes
- About
- About SBS
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- Legal Statement
Loop-mediated Isothermal Amplification (LAMP)
High-Performance LAMP Solutions for Molecular Diagnostics and Research
From next-generation Bst polymerases and lyophilized microbeads to complete CRISPR-compatible workflows, SBS Genetech provides one of the world's most comprehensive LAMP platforms.
What is Loop-mediated Isothermal Amplification (LAMP)?
Loop-mediated Isothermal Amplification (LAMP) is a rapid, highly sensitive, and highly specific nucleic acid amplification technology that enables DNA or RNA detection under a constant temperature. Unlike conventional Polymerase Chain Reaction (PCR), which relies on repeated thermal cycling, LAMP continuously amplifies target nucleic acids at a single temperature—typically between 60°C and 65°C—using a strand-displacing DNA polymerase and a specially designed set of primers.
Because the reaction does not require a thermal cycler, LAMP greatly simplifies molecular testing while maintaining excellent analytical performance. The technology has become one of the most widely adopted isothermal amplification methods for applications ranging from life science research to molecular diagnostics, food safety, veterinary testing, and point-of-care testing (POCT).
Today, LAMP serves as a core technology for rapid molecular detection, especially in scenarios where speed, portability, and operational simplicity are essential.

What Makes LAMP Different?
The fundamental difference between LAMP and conventional PCR lies in the amplification strategy.
PCR requires repeated cycles of DNA denaturation, primer annealing, and polymerase extension, making a precision thermal cycler indispensable. In contrast, LAMP performs continuous DNA synthesis at a constant temperature through the coordinated action of multiple primers and a strand-displacing DNA polymerase.
This isothermal mechanism not only simplifies instrument requirements but also significantly shortens assay time. In many applications, amplification can be completed within 15–30 minutes, allowing rapid molecular testing without sacrificing sensitivity or specificity.
For laboratories developing portable or decentralized diagnostic solutions, the ability to perform amplification using only a simple heating device represents one of LAMP's greatest advantages.

How Does LAMP Work?
LAMP utilizes four to six primers that recognize six to eight distinct regions on the target nucleic acid sequence. This unique primer design generates loop structures during amplification, enabling continuous self-primed DNA synthesis throughout the reaction.
Instead of repeatedly separating DNA strands through heating, LAMP relies on a strand-displacing DNA polymerase, such as Bst DNA polymerase, to synthesize new DNA while simultaneously displacing existing strands. This process rapidly produces large quantities of amplification products with exceptional efficiency.
For RNA targets, reverse transcriptase can be incorporated into the same reaction, allowing Reverse Transcription LAMP (RT-LAMP) to perform reverse transcription and DNA amplification in a single tube, reducing workflow complexity and minimizing contamination risk.
Why Has LAMP Become So Popular?
Several features have contributed to the rapid adoption of LAMP across both research and diagnostic applications:
Rapid amplification
Results are typically available within 15–30 minutes.
High analytical sensitivity
Efficient amplification enables detection of low-copy-number targets.
High specificity
Multiple primer recognition regions reduce non-specific amplification.
Simple instrumentation
Only a constant-temperature heat source is required.
Flexible detection formats
Compatible with fluorescence, colorimetric assays, turbidity measurement, lateral flow assays, and CRISPR-based detection.
Suitable for field deployment
Ideal for decentralized testing and resource-limited settings.
Where Is LAMP Used?
LAMP has become an important molecular tool across numerous research and industrial sectors, including:
Infectious Disease Diagnostics
Rapid detection of viral and bacterial pathogens
Point-of-Care Testing (POCT)
Portable molecular diagnostics outside centralized laboratories
Food Safety
Detection of foodborne microorganisms and contamination
Veterinary Diagnostics
Livestock and companion animal disease surveillance
Plant Pathology
Identification of crop pathogens and agricultural diseases
Environmental Monitoring
Water quality testing and microbial surveillance
Powering Next-Generation LAMP with Advanced Bst Polymerases
The evolution of LAMP has been closely linked to continuous advances in strand-displacing DNA polymerases, particularly Bst DNA polymerases, which serve as the foundation of efficient isothermal amplification. As LAMP applications have expanded from basic DNA detection to rapid RNA detection, RT-LAMP, multiplex assays, lyophilized molecular tests, and point-of-care diagnostics, next-generation polymerases have been engineered to deliver faster amplification kinetics, enhanced substrate compatibility, improved inhibitor tolerance, and greater reaction robustness.
At SBS Genetech, enzyme engineering is at the core of our LAMP technology platform. Our latest generation of advanced Bst polymerases integrates high amplification efficiency, Hot Start control, DNA/RNA co-amplification capability, and complete dUTP compatibility for carryover contamination prevention. These innovations provide researchers and diagnostic developers with a reliable foundation for developing fast, sensitive, and robust next-generation LAMP assays.

The Next Step in Bst Polymerase Evolution
As part of SBS Genetech’s LAMP enzyme engineering portfolio, Bst dU-P DNA/RNA Polymerase represents the culmination of multiple generations of optimization, combining hot-start control, DNA/RNA amplification capability, 65–70°C robustness, inhibitor tolerance, and 100% dUTP compatibility into a single next-generation platform.
Lyophilized LAMP Assay System Platform
Lyophilized LAMP Assay Systems are fully pre-mixed, freeze-dried molecular detection solutions designed to simplify nucleic acid amplification workflows while significantly improving reagent stability and transportability. By integrating all essential reaction components into a single lyophilized format, the system enables rapid deployment of DNA and RNA detection assays without the need for cold-chain storage or complex reagent preparation.
Built on SBS Genetech engineered LAMP enzyme technologies, including proprietary polymerase systems, the platform supports robust isothermal amplification across a wide range of diagnostic and research applications.
Available product formats include PrimeIAmp™ HotStart Bst dU-P Basic Microbeads (with UDG) for general-purpose LAMP workflows, and PrimeIAmp™ HotStart Bst dU-P Fluorescent Microbeads (with UDG) optimized for fluorescence-based real-time detection.

Loop-mediated Isothermal Amplification (LAMP) Products
Buy nowBst dU-P DNA/RNA Polymerase (glycerol-free)$280.00 - $1,856.00$2,320.00
Buy nowPrimeIAmp™ HotStart Bst dU-P Fluorescent Microbeads (with UDG)$500.00 - $2,000.00$2,500.00
Buy nowPrimeIAmp™ HotStart Bst dU-P Basic Microbeads (with UDG)$500.00 - $2,000.00$2,500.00
Buy nowBst dU‑P Fluorescent LAMP Lyophilized Mix$400.00 - $1,600.00$2,000.00
Buy nowBst dU‑P Basic LAMP Lyophilized Mix$400.00 - $1,600.00$2,000.00
Buy now4× Bst dU‑P Fluorescent LAMP Master Mix (glycerol-free)$400.00 - $1,600.00$2,000.00
Buy now4× Bst dU‑P Basic LAMP Master Mix (glycerol-free)$400.00 - $1,600.00$2,000.00
Buy nowMycoplasma Pneumoniae Fluorescence LAMP Assay Kit$196.00 - $596.00$745.00
Buy nowHotStart Bst P DNA/RNA Polymerase (glycerol-free)$280.00 - $1,856.00$2,320.00
Buy nowHotStart Bst DNA/RNA Polymerase (glycerol-free)$280.00 - $1,856.00$2,320.00
Buy nowPrimeIAmp™ HotStart LAMP Bst P L-HNB MasterMix$400.00 - $1,600.00$2,000.00
Buy nowPrimeIAmp™ HotStart Bst P DNA/RNA LHNB LyoMix (70ºC reaction)$660.00 - $2,000.00$2,500.00
Buy nowPrimeIAmp™ HotStart Bst P DNA/RNA Basic & SYBR Green LyoMix (70ºC reaction)$660.00 - $2,000.00$2,500.00
Buy nowPrimeIAmp™ HotStart Bst P DNA/RNA LHNB Microbead (70ºC reaction)$740.00$925.00
Buy nowPrimeIAmp™ HotStart Bst P DNA/RNA Basic Microbead (70ºC reaction)$740.00$925.00
Buy nowPrimeIAmp™ HotStart Bst DNA/RNA LHNB LyoMix (65ºC reaction)$660.00 - $2,000.00$2,500.00
Buy nowPrimeIAmp™ HotStart Bst DNA/RNA Basic & SYBR Green LyoMix (65ºC reaction)$660.00 - $2,000.00$2,500.00
Buy nowPrimeIAmp™ HotStart Bst DNA/RNA LHNB Microbead (65ºC reaction)$740.00$925.00
Buy nowPrimeIAmp™ HotStart Bst DNA/RNA Basic Microbead (65ºC reaction)$740.00$925.00Published Papers
Representative Publications Using SBS Genetech Isothermal Amplification Products
Xue, T. , Ma, Z. , Liu, F. , Du, W. , & An, C. . (2020). Pneumocystis jirovecii colonization and its association with pulmonary diseases: a multicenter study based on a modified loop-mediated isothermal amplification assay. BMC Pulmonary Medicine, 20(1).
Zhao, K. , Hu, R. , Ni, J. , Liang, J. , & Li, C. . (2020). Establishment of a porcine parvovirus (PPV) LAMP visual rapid detection method. Journal of Virological Methods, 284, 113924.
Papadakis, G. , Pantazis, A. K. , Fikas, N. , Chatziioannidou, S. , Tsiakalou, V. , & Michaelidou, K. , et al. (2022). Portable real-time colorimetric LAMP-device for rapid quantitative detection of nucleic acids in crude samples. Scientific Reports, 12(1), 1-15.
Wu, R. , Liu, X. , Guo, B. , Chen, F. , & Wang, X. . (2014). Development of double loop-mediated isothermal amplification to detect listeria monocytogenes in food. Current Microbiology, 69(6), 839-845.
Ji, J. , Du, L. Q. , Xie, Q. M. , Cao, Y. C. , & Bee, Y. Z. . (2009). Rapid diagnosis of duck plagues virus infection by loop-mediated isothermal amplification. Research in Veterinary Science, 87(1), 53-58.
Zhang, S. , Xu, X. , Wu, Q. , & Zhang, J. . (2013). Rapid and sensitive detection of pseudomonas aeruginosain bottled water by loop-mediated isothermal amplification. European Food Research & Technology, 236(1), 209-215.
Xu, X. , Zhang, S. , Wu, Q. , Zhang, J. , Li, F. , & Cheng, J. . (2014). Development and Application of a Loop-Mediated Isothermal Amplification (LAMP) Method for Rapid and Sensitive Detection of Enterococcus faecalis in Drinking Water. Journal of Food Safety, 34(2), 103–110.
Zhang, F. , Shi, Y. , Jiang, K. , Song, W. , Ma, C. , & Xu, Z. , et al. (2014). Rapid detection and quantification of Prorocentrum minimum by loop-mediated isothermal amplification and real-time fluorescence quantitative PCR. Journal of Applied Phycology, 26(3), 1379-1388.
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