Enhance your productivity with high-performance solutions for robust processing of samples in nanoscale reactions, enabling quick and reliable SNP genotyping, gene expression, digital PCR, hypothesis-free RNA sequencing and targeted amplicon library preparation. Our revolutionary integrated fluidic circuits (IFCs) enable automated molecular biology that significantly minimizes pipetting steps, hands-on time and reagent consumption while maximizing efficiency, cost savings and robust data production.
Manage sample identity and quality using microfluidics-based DNA fingerprinting
The Advanta™ Sample ID Genotyping Panel is a 96-SNP assay enabling laboratories to generate a sample-specific genetic fingerprint and quality assessment from research specimens throughout the sample journey. Developed for use with the Biomark™ HD system, the Advanta Sample ID Genotyping Panel delivers performance you can trust with workflow efficiencies that minimize hands-on time and reagent consumption.Learn More
DNA fingerprinting at a genetics biorepository
Kelly Nudelman and Tae-Hwi Schwantes-An discuss the importance of sample identification and quality control at the Indiana University Genetics Biobank.Read more
Enhance your productivity with reagents designed to maximize the power of Juno™, Biomark™ and EP1™ systems and reduce costs. The Juno workflow includes preamplification prior to genotyping, for an integrated process with minimal hands-on time. Use SNP Type™ or your existing TaqMan® assays with optimized reagents on all Fluidigm platforms.Learn more
Ideal for labs processing hundreds to thousands of samples, the Biomark™ HD system provides significant cost and time advantages over plate-based technologies. And with a wide range of integrated fluidic circuit (IFC) formats available, scaling from mid- to high-throughput on a single system is easily achievable.Learn more
RNA sequencing (RNA-seq) is the gold standard for hypothesis-free profiling of the transcriptome and is an essential tool for molecular biology laboratories. Designed to drive significant improvement in the RNA-seq workflow, the Advanta™ RNA-Seq NGS Library Prep Kit together with the Juno™ system provides an integrated solution for automated, cost-efficient NGS library prep.
Advanta RNA-Seq XT NGS Library Prep Kit (101-9950)
This kit uses a polyadenylated [poly(A)] enrichment approach to prepare NGS-ready, full-length cDNA libraries from total RNA. The kit contains sufficient 48.Atlas™ IFCs (4 per kit), reagents, Control Line Fluid, and unique dual indexes (UDIs) to generate libraries for 192 samples, and it includes 4 sets of 1–48 UDI barcodes.
Advanta RNA-Seq XT NGS Library Prep Kit II (101-9959)Learn more
This kit uses a polyadenylated [poly(A)] enrichment approach to prepare NGS-ready, full-length cDNA libraries from total RNA. The kit contains sufficient 48.Atlas™ IFCs (4 per kit), reagents, Control Line Fluid, and unique dual indexes (UDIs) to generate libraries for 192 samples, and it includes 2 sets of 1–48 UDI barcodes and 2 sets of 49–96 UDI barcodes.
Targeted DNA Sequencing
Accurately tracking samples from acquisition to data analysis is important for any laboratory, especially for translational and clinical research programs, biorepositories and centralized cell line banks. Implementing a standard genotyping workflow to confirm the identity and quality of each sample prior to analysis can increase your confidence in study results.Learn more
The Advanta™ FFPE RNA Extraction Kit provides an effective, nontoxic method for purifying total RNA from FFPE research samples. Optimized for isolation of high-molecular-weight RNA, the kit uses a bead-based RNA extraction method for RNA purification, helping to reduce the RNA damage that can occur with other methods.Learn more
Digital PCR (dPCR) on the Biomark™ system delivers unparalleled accuracy and real-time dPCR capabilities. The platform provides a choice of real-time or endpoint analysis and the capability to quantitate up to two targets per sample using multiple reporter dyes. Innovative software enables automated copy number variation measurement as well as quantitation.Learn more