Discover the Depths of Cellular Diversity with Single Cell RNA Sequencing
Unleash the full potential of cellular research with our cutting-edge single cell RNA seq (scRNA-seq) technology.
This advanced method transcends traditional bulk RNA sequencing by capturing the intricate heterogeneity of individual cells, revealing the hidden layers of cellular diversity.
Omics Empower Distinctive Advantage: Cutting-Edge Solutions
Leveraging the power of omics technologies, we are proud to unveil our distinctive advantage in the scientific arena. Here's a glimpse into the essence of our excellence!
Technological Superiority
Full-Length V(D)J information: We can stitch together to obtain the full-length information of the V(D)J region.
No V- or J-Specific Primers: This avoids the complex bias issues associated with multiplex PCR.
Comprehensive Cellular Insights: While obtaining each cell's V(D)J information, we can also acquire the transcriptome information of T cells and B cells simultaneously.
Sample Requirements of RNA Single Cell Sequencing
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Achievement Leader
We've translated and published over 300 articles, earned nearly 190 acknowledgments, and hold 15 authorship credits. Our leadership in multi-omics research, including single-cell and spatial analyses, is unparalleled.
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Experienced Innovators
With a track record of over 2000 projects, we've mastered the art of single-cell transcriptomics, handling 20,000+ specimens across a diverse range of tissues and plants.
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Committed to Quality
We rigorously evaluate sample quality to ensure robust data, going beyond basic checks to include fragment rates and cell health.
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Collaborative Service Model
Led by technical experts, our team provides comprehensive post-sale support, from data interpretation to article brainstorming, ensuring a seamless project experience.
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Swift and Personalized Service
Immediate access to our technical and analytical team, with unlimited analysis sessions included, tailored to your specific research needs.
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Dedicated Support
Our customer service is solution-driven, addressing post-sale issues promptly and effectively.
We are a global transcriptome sequencing service provider specializing in multi-omics solutions for life science research. With a strong foundation, we have supported 2,800+ research institutions and tens of thousands of clients, contributing to 5,000+ publications with a cumulative Impact Factor nearing 40,000.
