Scale single cell experiments without compromise. Evercode™ WT Penta empowers research with limitless possibilities by enabling the unbiased discovery of novel gene expression profiles and previously uncharacterized cell types.
Evercode™ split-pool combinatorial barcoding is a simple, instrument-free solution to single cell sequencing. This easily adopted approach brings unprecedented sensitivity, scalability, and flexibility to any lab.
Evercode's combinatorial barcoding enables you to dramatically scale up the cells and samples
per experiment.
遠心機、サーマルサイクラー、
ピペットがあれば、すぐに実験を
開始可能。
低発現遺伝子をより正確に検出し、
ドロップレット法に伴う環境RNAの
混入を回避。
固定したサンプルを最大6か月間、
保存でき、スケジュールに応じて
まとめて解析が可能。タイムコース
実験や拠点間の共同研究に最適。
Multiplets introduce noise and compromise the integrity of single cell data. With Evercode technology, where the cell itself is the reaction vessel, doublet rates remain consistently low across all our kits—ensuring cleaner, more reliable data. This means higher confidence in rare cell population detection, more precise clustering, and better overall resolution of cellular heterogeneity.
With Evercode’s fixation technology, researchers can preserve biological states at the moment of collection, regardless of species, locking in gene expression profiles. This flexibility means samples don’t need to be processed immediately, allowing labs to coordinate with core facilities, or scale up experiments without logistical constraints. By fixing now and processing later, researchers can more feasibly expand their studies—exploring more samples, conditions, or time points—without sacrificing data quality.
The Evercode™ Whole Transcriptome solution provides the reagents, software, and support to pursue difficult research questions from bench to insight.
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 Trailmaker platform provides an end-to-end data analysis experience, guiding you from FASTQ files to publication-ready figures, while maintaining the flexibility of multiple data entry and exit points. Our computational pipeline continues to also be available.
More information and literature across the entire range of Parse Biosciences products.
Reach out for a quote or for help planning your next experiment.
