Cells
Samples
Explore a wide variety of adaptive immunity applications with Evercode™ BCR - the only instrument-free, fixed sample BCR profiling solution that detects full-length, natively paired heavy and light chain sequences to comprehensively characterize the BCR repertoire.
Explore datasetsCells
Samples
Up to 10K cells, 1-12 samples
10K-100K cells, 1-48 samples
100K-1M cells, 1-96 samples
Up to 10K cells, 1-12 samples
10K-100K cells, 1-48 samples
100K-1M cells, 1-96 samples
Reveal the full complexity of the immune repertoire with sensitive detection of BCRs. Measure transcriptome-wide gene expression together with full-length paired heavy and light sequences and isotypes in the same cells.
Scale up your experiments to capture the full complexity of the immune repertoire. Here, Evercode BCR simultaneously profiled over a million isolated human B cells from 24 donors including individuals with Type-1 Diabetes, Multiple Sclerosis, Rheumatoid Arthritis, Crohn's, and Celiac disease.
As the only all-in-one solution for humanized transgenic mice, Evercode BCR delivers unprecedented resolution of human-mouse chimeric BCRs in Atlas™ mice revealed 35% class-switched clonotypes of plasmablasts following tetanus toxoid immunization.
Resolution of paired full-length heavy and light chain BCRs is essential for classifying B cell clonality. In an experiment profiling T1D and control donors, Evercode BCR captured both heavy and light chains with 87-89% BCR pairing efficiency.
The Evercode BCR kit generated the most comprehensive immune repertoire detection from a single experiment to date. Over 900,000 unique paired clonotypes were identified across the 24 donors with the vast majority being classified as unique clonotypes.
The Evercode™ BCR solution provides the reagents, software, and accessibility to pursue difficult research questions.
Lock in gene expression immediately after sample collection with a rapid fixation protocol. After fixation, samples can be stored for up to 6 months or proceed directly to barcoding.
Append barcodes to each transcript by progressing cells through a streamlined split-pool combinatorial barcoding process, which produces sequencing-ready libraries.
The resulting libraries are sequenced by NGS.
Our computational pipeline generates an interactive report for rapid insights. All output data files, including gene-cell count matrix, integrate seamlessly with existing open source tools such as Seurat or Scanpy.
Read more about the technology and dive deeper into the technical details.
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