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    10x Genomics Single Cell RNA-Seq

      10x Genomics single cell RNA-seq is a high-throughput single-cell transcriptome sequencing platform developed by 10x Genomics, based on droplet microfluidics technology. This technique enables the in situ labeling and sequencing of RNA molecules from tens of thousands of individual cells in a single experiment, thereby reconstructing the cellular composition, subpopulation distribution, and gene expression profiles of complex tissues at single-cell resolution. This groundbreaking approach has fundamentally transformed our understanding of cellular heterogeneity, allowing researchers to move beyond traditional “bulk average” measurements and investigate cell-to-cell differences in biological processes such as development, disease progression, and environmental responses. Today, 10x Genomics single cell RNA-seq is widely used in cutting-edge fields such as oncology, neuroscience, immunology, and stem cell research, and it serves as a key technological driver for advances in precision medicine and systems biology.

       

      The primary advantage of 10x Genomics single cell RNA-seq lies in its unparalleled ability to resolve cellular heterogeneity. Conventional RNA sequencing methods can only provide average expression levels across a mixed population of cells, making it difficult to detect gene expression differences among distinct cell types or to identify rare cell populations. In contrast, 10x Genomics single cell RNA-seq captures the transcriptomes of individual cells, enabling the discovery of hidden cell subtypes, cellular states, and functional phenotypes within complex systems. It further facilitates the reconstruction of differentiation trajectories and the identification of key regulatory factors driving cellular transitions.

       

      The core of 10x Genomics single cell RNA-seq technology lies in its unique microfluidic system and barcoding strategy. Each cell is encapsulated within an individual aqueous droplet containing a preloaded magnetic bead. These beads are coated with cell-specific barcodes and molecular indices. Upon cell lysis inside the droplet, RNA is captured by the beads and reverse-transcribed into cDNA, during which the barcodes are incorporated into the resulting sequences. This design allows every sequencing read to be accurately traced back to its cell of origin, while minimizing PCR amplification bias, thereby enabling highly precise quantification. This integrated system provides researchers with comprehensive and reliable single-cell transcriptomic data, dramatically enhancing both the depth and breadth of downstream analysis.

       

      From a workflow perspective, 10x Genomics single cell RNA-seq requires stringent control over sample preparation, cell viability, and instrument operation. First, it is essential to obtain a well-dispersed, aggregation-free suspension of viable cells, and assess their status through filtration and staining. During droplet generation, single-cell encapsulation must be carefully controlled to avoid multiplet artifacts that can confound data interpretation. Library construction and high-throughput sequencing must be carried out using proprietary reagents and standardized protocols to ensure data quality and consistency. Therefore, the success of 10x Genomics single cell RNA-seq not only depends on the hardware platform, but also on meticulous sample handling and systematic experimental control.

       

      MtoZ Biolabs, leveraging its advanced technological platforms and expert bioinformatics team, provides high-quality, standardized single-cell sequencing services. These services cover the full workflow—from sample preprocessing, library preparation, and sequencing to data analysis and scientific support—ensuring reliable results and robust insights for your research.

       

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

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