

Microfluidic Chip-Based Cell Sorter
微流控芯片式细胞分选仪
- SKU CSO-0003
- Cell Sorters
- CE (to be confirmed)
- IEC 61010-1 compliance (to be confirmed)
- ISO 13485 manufacturing (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Sorting mechanism | Piezo or pneumatic valve in disposable chip |
|---|---|
| Laser configuration | 1–3 (405/488/561/640 nm) |
| Fluorescence channels | Up to 8 |
| Channel width | Approx. 50–100 µm |
| Maximum sort rate | 2,000–20,000 events/s |
| Sort purity | Above 90–95% (typical) |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ISAC Cell Sorter Biosafety Standards, IEC 61010-1, IEC 60825-1
What is the Microfluidic Chip-Based Cell Sorter?
A microfluidic chip-based cell sorter performs sorting inside a sealed, disposable cartridge using valves or actuators instead of charged droplets. It lowers aerosol risk, avoids cross-contamination between samples and handles fragile cells at gentle pressures, suiting clinical-grade and biosafety-sensitive workflows.
What is the Microfluidic Chip-Based Cell Sorter?
A microfluidic chip-based cell sorter performs sorting inside a sealed, disposable cartridge using valves or actuators instead of charged droplets. It lowers aerosol risk, avoids cross-contamination between samples and handles fragile cells at gentle pressures, suiting clinical-grade and biosafety-sensitive workflows.
Overview
Microfluidic sorters move the sort decision into a disposable chip with microchannels, typically 50 to 100 micrometers wide, in which a piezoelectric actuator, pneumatic valve or similar switch diverts target cells into a collection channel. Because the sample path is sealed within a cartridge, there is no droplet jet and no aerosol generation, and each sample uses a fresh flow path, eliminating carry-over and eliminating the need for decontamination between runs. Pressures are lower than jet-in-air systems, which improves viability of delicate cells such as primary neurons, stem cells and cells for cell therapy. Typical sort rates are 2,000 to 20,000 events per second, with one to three lasers and up to 8 fluorescence channels. Cartridge cost per sample adds to running expense, and sort rate is lower than high-speed droplet systems.
How does it work?
Sorters analyze cells like an analyzer, then apply a decision in real time. In droplet sorters, a piezoelectric transducer vibrates the nozzle at 20 to 100 kHz so the stream breaks into uniform droplets just after the laser intercept. When a cell matching the sort gate is about to be enclosed, the electronics apply a charge to the stream, and the droplet separates carrying that charge. Charged droplets pass through high-voltage deflection plates and fall into tubes or multiwell plates, while uncharged droplets go to waste. A drop delay calibrated with fluorescent beads defines the time between detection and droplet break-off. Microfluidic chip sorters instead use valves, piezo actuators or optical forces inside a disposable cartridge, enclosing the sample away from aerosols.
What are the key features?
- Sealed disposable cartridge eliminates aerosol generation and sample cross-contamination
- Low operating pressure preserves viability of fragile primary and stem cells
- Fresh fluid path per sample removes the need for decontamination between runs
- One to three lasers with up to 8 fluorescence channels
- Sort rates of 2,000 to 20,000 events per second for routine populations
- Suitable for installation in a biosafety cabinet or cleanroom suite
What are the technical specifications?
A typical microfluidic chip-based cell sorter configuration offers sorting mechanism of Piezo or pneumatic valve in disposable chip, laser configuration of 1–3 (405/488/561/640 nm), fluorescence channels of Up to 8, channel width of Approx. 50–100 µm, maximum sort rate of 2,000–20,000 events/s and sort purity of Above 90–95% (typical). Values are indicative of the product class; the exact figures for each configuration are confirmed on the quotation and the calibration documents supplied with the instrument.
Which applications is it used for?
The Microfluidic Chip-Based Cell Sorter is used in cell therapy product development, primary neuron and stem cell sorting, sorting infectious or viral vector-transduced cells, sorting in biosafety cabinets and small-volume precious sample sorting. Across the wider Cell Sorters class, laboratories also deploy it for stem cell and progenitor enrichment, single-cell cloning of engineered cell lines and sorting for single-cell RNA sequencing.
Which standards and certifications apply?
Relevant standards and methods include ISAC Cell Sorter Biosafety Standards, IEC 61010-1, IEC 60825-1, EN 12469, ISO 14698-1, CLSI H62 and ISAC FCS 3.1. Certification candidates for this model are CE, IEC 61010-1 compliance and ISO 13485 manufacturing; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Sorters need a clean, temperature-stable room, compressed air or nitrogen supply and often a dedicated operator. Perform daily setup with calibration beads to set drop delay, verify stream stability and check sort accuracy. Decontaminate fluidics with bleach or dedicated cleaning solutions before and after every sample and sterilize sheath paths for primary cell work. Sorting human or infectious material requires a biosafety assessment, with containment verified by an aerosol test such as potassium iodide or fluorescent bead methods. Nozzles, O-rings and sheath filters are consumables and should be replaced on a schedule. Laboratories should log sorts, purity checks and preventive maintenance to support reproducibility and audits.
How do I select the right Microfluidic Chip-Based Cell Sorter?
Choose a chip-based sorter when biosafety, contamination control or gentle handling outweighs maximum speed, for instance in cell therapy development. For multi-way sorting or large panels, a droplet sorter is better. In an RFQ specify chip type, sterility, sort speed, laser set and validation documentation.
How does it compare with other Cell Sorters variants?
Choose a sorter on purity, yield, viability and containment requirements. Determine how many populations you need to collect at once, since two-way, four-way and six-way sorting require different deflection hardware. Match nozzle size, from 70 to 130 micrometers, to cell size and fragility; larger nozzles and lower pressure are gentler for primary cells. Check sort speed, typically 20,000 to 70,000 events per second, against the abort rate and recovery. For infectious, human primary or viral vector samples, specify an aerosol-managed or enclosed system and a class II biosafety cabinet. Consider single-cell deposition into 96 or 384-well plates, index sorting, number of lasers, and ease of use. Also confirm sterile fluidics cleaning and availability of service engineers.
Full specifications
| Sorting mechanism | Piezo or pneumatic valve in disposable chip |
|---|---|
| Laser configuration | 1–3 (405/488/561/640 nm) |
| Fluorescence channels | Up to 8 |
| Channel width | Approx. 50–100 µm |
| Maximum sort rate | 2,000–20,000 events/s |
| Sort purity | Above 90–95% (typical) |
| Operating pressure | Below 10 psi |
| Sort streams | 2 (target and waste) |
| Sample volume | 100 µL–several mL |
| Consumable | Single-use sterile sort chip |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Cell therapy product development
- Primary neuron and stem cell sorting
- Sorting infectious or viral vector-transduced cells
- Sorting in biosafety cabinets
- Small-volume precious sample sorting
Key features
- Sealed disposable cartridge eliminates aerosol generation and sample cross-contamination
- Low operating pressure preserves viability of fragile primary and stem cells
- Fresh fluid path per sample removes the need for decontamination between runs
- One to three lasers with up to 8 fluorescence channels
- Sort rates of 2,000 to 20,000 events per second for routine populations
- Suitable for installation in a biosafety cabinet or cleanroom suite
Frequently asked questions about Microfluidic Chip-Based Cell Sorter
The sample never leaves a sealed cartridge, so there is no high-pressure jet breaking into droplets in open air. Sorting happens by valves or actuators in microchannels, which removes the main source of biohazardous aerosols generated by conventional droplet sorters.
Generally yes. Operating pressures are much lower than jet-in-air droplet sorters and there is no electrostatic charging or droplet impact, which can improve post-sort viability for fragile primary cells. Results still depend on sample handling and chip design.
Sort speed is lower than high-speed droplet sorters, typically under 20,000 events per second, and most systems provide two-way sorting with fewer colors. Each run also uses a single-use chip, which adds consumable cost and requires sterile storage.
It analyzes each cell by scatter and fluorescence, then a vibrating nozzle breaks the stream into droplets. Droplets containing cells that meet the sort gate are electrically charged and deflected by high-voltage plates into collection tubes or plates, leaving unwanted cells in waste.
Purity above 95 percent is common for well-separated populations sorted in purity mode, while yield and recovery are lower at high event rates. Actual results depend on gating, sample quality, sort mode, nozzle size and the abundance of target cells.
Sorting applies shear, pressure and electrostatic stress, so some loss of viability is possible. Using larger nozzles, lower sheath pressure, cooled collection, protein-supplemented collection media and lower event rates can preserve viability and downstream function for fragile primary cells.
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