CLindex: a sample multiplexing method for single cell transcriptomic analysisWatch nowLeave no cell behind:How to overcome the limitations of sample multiplexing, to remove species and cell-type bias, using a completely, antibody-independent new method based on “click chemistry”. This ground-breaking method will ensure that you capture the most cells types, including those that are prone to degradation, without limitation on the species. Our new solution, CLindex, is a new sample multiplexing method developed to help exactly with that.Using Singleron’s CLindex Kit for sample multiplexing offers several benefits:Increased Sample Throughput: You can pool up to 16 samples and capture genetic information from up to 120,000 cells on a single chip. This significantly boosts the number of samples you can process in one experiment.Reduced Batch Effects: By pooling multiple samples into a single experiment, CLindex® helps minimize batch effects, leading to more consistent and reliable results.Efficient and Unbiased Tagging: The technology employs click-chemistry for sample tagging, which is both efficient and unbiased. This ensures that each sample is accurately labeled without introducing significant biases.Cost-Effective: Combining multiple samples into one experiment reduces the overall cost of reagents and consumables.Single Cell Resolution: CLindex® allows for the analysis of the transcriptome at single cell resolution, providing detailed insights into cellular functions and interactions.These advantages make CLindex® a powerful tool for researchers looking to maximize their sample processing efficiency and data quality.Check out our latest webinars Learn more B2B-RARE Bench to Bedside: Understanding and Personalizing Treatment for Rare Neuromuscular Diseases In the European Union alone, around 36 million people live with a rare disease. And that number sounds almost contradictory. How can something rare affect… Read more Podcast: Why everyone needs bioinformatics skills now Why are bioinformatics skills becoming essential for every life scientist? And how is AI changing the way researchers analyze biological data? In the third episode… Read more Beyond Standard Single Cell Sequencing: Adding a New Dimension to Biological Discovery Standard single cell RNA sequencing is a powerful starting point in life science research, but it only tells part of the story. In this webinar,… Read more
B2B-RARE Bench to Bedside: Understanding and Personalizing Treatment for Rare Neuromuscular Diseases In the European Union alone, around 36 million people live with a rare disease. And that number sounds almost contradictory. How can something rare affect… Read more
Podcast: Why everyone needs bioinformatics skills now Why are bioinformatics skills becoming essential for every life scientist? And how is AI changing the way researchers analyze biological data? In the third episode… Read more
Beyond Standard Single Cell Sequencing: Adding a New Dimension to Biological Discovery Standard single cell RNA sequencing is a powerful starting point in life science research, but it only tells part of the story. In this webinar,… Read more