LeXPrep IGTR Multiplex PCR Library Prep Kit utilizes multiplex amplification to efficiently enrich the complementarity-determining regions (CDR3) across seven human adaptive immune receptor loci: IGH, IGK, IGL, TRA, TRB, TRG, and TRD. Paired with high-throughput sequencing, this kit enables high-resolution detection of B-cell and T-cell diversity and clonality. It is compatible with both DNA and cDNA from diverse sources, making it a versatile solution for immune repertoire profiling, lymphoid malignancy analysis, and minimal residual disease (MRD) monitoring.

LeXPrep EZ RNA Library Preparation Kit is a high-speed solution engineered for mainstream NGS platforms. It efficiently converts 2.5–500 ng of RNA—sourced from cells, fresh tissues, blood, microbes, or FFPE—into premium sequencing libraries. Whether you are performing gene expression profiling, fusion gene analysis, or RNA pathogen detection, LeXPrep delivers the reliability your research demands.

LeXPrep Single Cell WGA Kit: High-Fidelity Whole Genome Amplification

The LeXPrep Single Cell WGA Kit is a high-performance solution engineered for the robust whole-genome amplification (WGA) of genomic DNA from single cells or ultra-low input samples. Utilizing a proprietary system of optimized buffers and high-fidelity enzymes, this kit enables researchers to move from raw cells to microgram-level gDNA in just 3 hours.

Optimized for Precision and Yield

The kit features a streamlined, three-step workflow—Cell Lysis, Preamplification, and Amplification—designed to generate high-quality genomic material with exceptional coverage and uniformity. By minimizing sequence bias, the LeXPrep system ensures the highest accuracy for downstream variant calling and structural analysis.

HLA Typing: The Gateway to Precision Medicine

The Human Leukocyte Antigen (HLA) system is the biological “ID card” of the human immune system. Located on chromosome 6, this highly diverse genetic region is responsible for how our bodies recognize and respond to threats. Because HLA is the most polymorphic part of the human genome, its complexity requires expert precision.

At the intersection of immunology and innovation, accurate HLA typing is the decisive factor in:

• Life-Saving Transplants: Ensuring perfect compatibility for organ, bone marrow, and stem cell success.
• Next-Gen Oncology: Predicting and enhancing the efficacy of personalized cancer immunotherapies.
• Safety & Screening: Identifying population-specific responses to vaccines and critical drug treatments.

Unlock the full potential of your research and clinical outcomes with high-resolution HLA insights.

LeXPrep Methyl Library Preparation Kit v2: High-Performance Epigenetic Profiling

The LeXPrep Methyl Library Preparation Kit v2 is a sophisticated solution engineered for the construction of high-quality methylation sequencing (Methyl-Seq) libraries from double-stranded DNA (dsDNA). Optimized for both Illumina and MGI platforms, this kit provides researchers with the high-fidelity tools necessary to uncover the complex epigenetic landscape with precision and efficiency. Whether performing Whole-Genome Bisulfite Sequencing (WGBS) or hybrid capture-based targeted methylation sequencing, the LeXPrep v2 kit delivers consistent, high-resolution data. It is designed to work seamlessly with our LeXPress hybrid capture system, ensuring superior enrichment of targeted methylated regions.

LeXso AML MRD Comprehensive Solution: Ultra-Sensitive Monitoring for Acute Myeloid Leukemia

The LeXso AML MRD Comprehensive Solution is a high-performance platform based on advanced liquid-phase hybridization target enrichment technology. Specifically engineered for adult Acute Myeloid Leukemia (AML) Minimal Residual Disease (MRD) research, this solution provides the sensitivity and speed required to track low-frequency clones and assess molecular response with clinical-grade precision.

High-Sensitivity, Same-Day Workflow

By combining adapter identifiers with the patented LeXso hybrid capture system, this solution eliminates background noise and sequencing artifacts to achieve ultra-high detection sensitivity. The streamlined chemistry is designed for high-velocity laboratories, enabling the entire experimental process—from library to results—to be completed within a single day.

Targeted Precision: LeXso AML Panel v1.0

At the core of this solution is the LeXso AML Panel v1.0, a highly curated 42.5 Kb targeted panel covering 32 essential genes associated with adult AML. The panel is designed to detect a comprehensive range of variants, including:

• Base Substitutions (SNVs)
• Insertions and Deletions (Indels)
• Internal Tandem Duplications (e.g., FLT3-ITD)
• Critical Gene Fusions