Tissue Dissociation · Tissue Dissociation
MicroJet dissociation technology，15min to achieve90%tissue utilization。from micro-biopsies to dense solid tumors，one instrument coveringTissue Dissociation、cell washing、staining、sorting、nucleic acid extractionfull workflow — maximizing output from every precious sample。
UsingMicroJet dissociation technology，dissociation achievingCell Viability>90%*。breaks through limitations on dense tissues（solid tumors、fibrotic organs），ensuring zero waste of precious samples。processes samples as small as1mgSample，(biopsy-compatible)。
Intelligent variable-frequency mode，one instrument forTissue Dissociation、cell washing、cell staining、target cell sorting（magnetic bead method）、nucleic acid extraction。Contact-free、low-damage，for higher viability、and more complete cell populations。
15 minutes to 90% tissue utilization, dramatically boosting single-cell preparation efficiency.
Gentle rapid dissociation, primary cell viability >85% (vs. 60-70% conventional). Flexible control — from high-viability single cells to preserved micro-spheroids for organoid construction.
scRNA-seq confirmed: rare immune cell (<0.1%) detection sensitivity enhanced for perfect tumor microenvironment profiling.
Tissue-type-specific optimized enzyme systems，with proprietary formulations。gentle yet efficient protection ofCell Viabilityand membrane protein epitopes，for enhanced yield and integrity。
*Trypan blue/PI double staining, n=1000
High-quality single-cell suspension is critical for organoid culture success. The MicroJet Dissociator provides standardized solutions with gentle dissociation, efficient enrichment, and precise control.
Near 100% cell viability with instrument-assisted processing (vs. 25–45% manual). Cell yields up to 3.0×10⁷ (vs. 1.6×10⁷ manual). FACS-sorted AT2 cells for organoid models with significantly enhanced culture stability.
MicroJet mixing accelerates antibody binding — 4× faster staining vs. static incubation. Staining ratios improved ~120% and ~200% for low and high expression antigens respectively.
Superior yield, viability, and dispersion vs. conventional methods for kidney, bladder, cornea, and muscle tissues. >95% membrane protein epitope retention (CD9/CD10) for flow sorting and spatial proteomics.
72h proliferation at 92% of fresh cells, 1.3× day-1 attachment, 1.2× proliferation rate vs. conventional methods.
Full-scenario customization — single/multi-channel, washing, staining modes for various tube formats. Optional temperature control and multi-channel throughput modules. From exploratory research to high-throughput screening, one instrument covers all needs.
Harvard Medical School · Yale University · Tsinghua University · UMass · Max Planck Institute · University of Twente · University of Rome
Schedule a demo，witness15minTissue Dissociationefficiency and gentleness
