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    10x BCR Sequencing

      10x BCR sequencing is an advanced genomic technology specifically designed to investigate the complexity and dynamic changes of B cell receptors (BCRs). BCRs are essential components of the human immune system, responsible for recognizing and binding to foreign antigens, thereby initiating immune responses. By leveraging 10x BCR sequencing, researchers can gain in-depth insights into the processes of BCR gene recombination and somatic hypermutation, revealing how individual immune systems adapt to and combat diverse pathogens and diseases.

       

      This technology has demonstrated broad potential across various domains, including basic immunology, disease diagnostics, and personalized medicine. In fundamental research, it enables scientists to dissect B cell development, identify novel antibody structures, and advance the understanding of mechanisms underlying immune memory formation. By analyzing BCR sequence data, researchers can trace specific B cell clones and their evolutionary trajectories, providing a dynamic view of immune responses. These insights are crucial for elucidating how the immune system maintains homeostasis and responds to external challenges.

       

      Clinically, 10x BCR sequencing offers valuable applications in disease monitoring and therapeutic assessment. By profiling a patient's BCR repertoire, clinicians can obtain detailed information about disease status and monitor treatment efficacy in real time. Furthermore, 10x BCR sequencing helps identify potential therapeutic targets, thereby supporting precision medicine efforts. For example, in cancer treatment, characterizing specific BCR variants may inform the design of more targeted therapeutic strategies and improve clinical outcomes. In the context of personalized medicine, deep analysis of a patient’s BCR repertoire enables the development of tailored treatment plans, minimizing unnecessary side effects while enhancing therapeutic effectiveness. This customized approach not only improves patient comfort but also elevates the overall standard of health management.

       

      Technical Workflow of 10x BCR Sequencing

      1. Sample Preparation

      The process begins with the collection of a sufficient number of B cells from patients or study subjects. B cells are typically enriched using flow cytometry or magnetic bead-based separation. The cells are then lysed, and RNA is extracted to ensure the integrity and purity of the sequencing templates.

       

      2. Library Construction

      Following sample preparation, sequencing libraries are constructed. This involves amplification of BCR genes and incorporation of unique barcodes, allowing for the individual identification and analysis of BCR sequences from each single B cell.

       

      3. High-Throughput Sequencing

      High-throughput sequencing constitutes the core of the 10x BCR workflow. Using highly efficient sequencing platforms, large-scale BCR sequence data can be rapidly generated. These datasets include not only sequence information but also expression levels and mutation profiles, providing a robust foundation for downstream bioinformatic analyses.

       

      Advantages and Challenges of 10x BCR Sequencing

      1. Advantages

      10x BCR sequencing offers several distinct advantages. One key strength is its high resolution, enabling single-cell level analysis and providing a detailed map of the immune landscape. Its high-throughput capability allows for simultaneous analysis of multiple samples, optimizing both time and cost efficiency. Moreover, the technology delivers high-quality sequence data, facilitating comprehensive understanding of BCR diversity and function.

       

      2. Challenges

      Despite these advantages, 10x BCR sequencing also presents notable challenges. Chief among them is the complexity of data analysis. Given the vast volume of sequencing data produced, advanced bioinformatics tools are essential for processing and interpretation. Additionally, the quality and quantity of input samples can significantly influence both the success rate of sequencing and the reliability of the results.

       

      At MtoZ Biolabs, we combine deep expertise with extensive experience to deliver high-quality sequencing outcomes and end-to-end technical support. Our team is dedicated to empowering clients to achieve breakthroughs in both research and clinical applications. Choosing MtoZ Biolabs means partnering with a trusted and professional ally. We look forward to collaborating with you to explore the frontiers of life science and help realize your scientific and translational goals.

       

      MtoZ Biolabs, an integrated chromatography and mass spectrometry (MS) services provider.

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