

Compact Personal Flow Cytometer
紧凑型个人流式细胞仪
- SKU FCY-0005
- Flow Cytometers
- CE (to be confirmed)
- IEC 61010-1 compliance (to be confirmed)
- ISO 9001 manufacturing (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Laser configuration | 1–2 (488 nm; optional 640 nm) |
|---|---|
| Fluorescence channels | 3–6 |
| Scatter parameters | FSC, SSC |
| Maximum event rate | 5,000–10,000 events/s |
| Sample volume | 50–300 µL per tube |
| Fluorescence sensitivity | FITC approx. 300 MESF (typical) |
By Lab Manufacturers China Technical TeamLast reviewed Standards: CLSI H62, CLSI H43, ISO 20391-1
What is the Compact Personal Flow Cytometer?
A compact personal flow cytometer is a small, low-maintenance analyzer with one or two lasers and three to six fluorescence channels. It gives individual labs and teaching environments straightforward access to viability, GFP, apoptosis and simple phenotyping assays without a dedicated cytometry facility.
What is the Compact Personal Flow Cytometer?
A compact personal flow cytometer is a small, low-maintenance analyzer with one or two lasers and three to six fluorescence channels. It gives individual labs and teaching environments straightforward access to viability, GFP, apoptosis and simple phenotyping assays without a dedicated cytometry facility.
Overview
Compact personal cytometers are designed for individual laboratories, teaching settings and satellite sites. They typically use a 488 nm laser, sometimes with a 640 nm red laser, and three to six fluorescence channels in fixed filter configurations, together with forward and side scatter. Enclosed fluidics, simplified startup and cleaning, and touch-screen or laptop software lower the training burden. Event rates of 5,000 to 10,000 per second are sufficient for routine assays such as viability with propidium iodide, GFP transfection, annexin V apoptosis and basic CD4 or CD8 counting. The footprint is often under 40 centimeters wide, and some models run on a small sheath supply. Compared with benchtop systems they offer fewer colors, less upgrade capacity and lower sensitivity for dim markers, but they need little infrastructure and less service.
How does it work?
A flow cytometer uses sheath fluid to hydrodynamically focus a sample into a narrow core stream so cells cross the laser interrogation point one at a time. Scattered light is collected at small angles (forward scatter, related to size) and at 90 degrees (side scatter, related to granularity). Fluorochromes are excited by lasers, commonly 405, 488, 561 and 640 nm, and emission is split by dichroic filters and bandpass filters to photomultiplier tubes or photodiodes. Conventional instruments assign one detector per fluorochrome and apply a compensation matrix, whereas spectral instruments capture the full emission spectrum and unmix it mathematically. Electronics digitize pulse height, area and width, and software records list-mode FCS files for gating and statistical analysis.
What are the key features?
- Compact enclosed unit under about 40 cm wide suits a crowded bench
- One or two lasers with three to six fixed-filter fluorescence channels
- Simplified startup and cleaning routine reduces training time for new users
- Touch-screen or laptop software with ready-made assay templates
- Event rates of 5,000 to 10,000 per second for routine assays
- Low sheath consumption and small waste volume per run
What are the technical specifications?
A typical compact personal flow cytometer configuration offers laser configuration of 1–2 (488 nm; optional 640 nm), fluorescence channels of 3–6, scatter parameters of FSC, SSC, maximum event rate of 5,000–10,000 events/s, sample volume of 50–300 µL per tube and fluorescence sensitivity of FITC approx. 300 MESF (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 Compact Personal Flow Cytometer is used in teaching laboratories, viability and apoptosis screening, GFP and transfection efficiency checks, basic CD4/CD8 counting and satellite and field laboratories. Across the wider Flow Cytometers class, laboratories also deploy it for immunophenotyping of lymphocyte subsets, CD34 stem cell enumeration and cell cycle and apoptosis analysis.
Which standards and certifications apply?
Relevant standards and methods include CLSI H62, CLSI H43, ISO 20391-1, IEC 61010-1, IEC 61010-2-101, IEC 60825-1 and ISAC FCS 3.1. Certification candidates for this model are CE, IEC 61010-1 compliance and ISO 9001 manufacturing; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Install the cytometer on a vibration-free bench with stable power and ambient temperature between 15 and 30 degrees Celsius, and provide waste handling for potentially biohazardous effluent, typically with bleach treatment. Run daily quality control using fluorescent beads to verify laser alignment, sensitivity and coefficient of variation, and keep Levey-Jennings style records of detector voltages. Perform daily and weekly fluidics cleaning to avoid clogging, and replace sheath filters and tubing on schedule. Laser power and optical alignment should be checked by trained service staff at least annually. Laboratories working under ISO 15189 or GLP should enable audit trails, electronic signatures and validated software updates.
How do I select the right Compact Personal Flow Cytometer?
Choose a compact personal cytometer when your assays use four colors or fewer, sample numbers are modest and there is no cytometry core nearby. For multi-color panels or regulated clinical work select a benchtop or high-parameter analyzer. In an RFQ state required colors, event rate, software templates and training and service coverage.
How does it compare with other Flow Cytometers variants?
Select a cytometer by panel complexity, sensitivity and workflow. Define the maximum number of simultaneous colors, then choose laser and detector count to match; conventional filter-based systems are simple for 4 to 12 colors, while spectral systems ease panel design beyond 20. Check resolution of dim populations, small particle detection and event rate, typically 10,000 to 100,000 events per second. Consider footprint, whether a compact personal analyzer or a full research platform is required, and whether an acoustic focusing or plate loader is needed for throughput. Verify that software provides compensation or unmixing, batch analysis and user access control. For clinical use, confirm that the supplier can support IVD documentation, calibration beads and a validated quality control routine.
Full specifications
| Laser configuration | 1–2 (488 nm; optional 640 nm) |
|---|---|
| Fluorescence channels | 3–6 |
| Scatter parameters | FSC, SSC |
| Maximum event rate | 5,000–10,000 events/s |
| Sample volume | 50–300 µL per tube |
| Fluorescence sensitivity | FITC approx. 300 MESF (typical) |
| Warm-up time | Under 10 min |
| Footprint | Approx. 35 × 45 × 40 cm |
| Weight | Approx. 20–30 kg |
| Power supply | 100–240 V AC, 50/60 Hz |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Teaching laboratories
- Viability and apoptosis screening
- GFP and transfection efficiency checks
- Basic CD4/CD8 counting
- Satellite and field laboratories
Key features
- Compact enclosed unit under about 40 cm wide suits a crowded bench
- One or two lasers with three to six fixed-filter fluorescence channels
- Simplified startup and cleaning routine reduces training time for new users
- Touch-screen or laptop software with ready-made assay templates
- Event rates of 5,000 to 10,000 per second for routine assays
- Low sheath consumption and small waste volume per run
Frequently asked questions about Compact Personal Flow Cytometer
Individual research groups, teaching laboratories and small satellite sites with simple assays such as viability, GFP expression, apoptosis or basic subset counting. Laboratories needing many colors, rare-event sensitivity or clinical validation are better served by a benchtop or high-parameter analyzer.
Most compact models detect three to six fluorescence colors in addition to forward and side scatter, using one or two lasers and fixed filter sets. This is enough for viability, GFP plus a few surface markers, or simple apoptosis assays.
Usually not. Automated startup, cleaning and template-based acquisition let trained laboratory staff run the instrument, though daily quality control with beads, periodic fluidics maintenance and annual service are still recommended to keep data comparable over time.
A flow cytometer measures forward scatter, side scatter and fluorescence intensity from each cell or particle. These signals report relative size, internal complexity and the presence or amount of fluorescently labeled markers, enabling counting, phenotyping and functional analysis at rates of thousands of cells per second.
Conventional cytometers use optical filters to direct a defined wavelength band to each detector and then compensate for overlap. Spectral cytometers record the whole emission spectrum across many detectors and unmix it, which allows more colors per panel and use of autofluorescence extraction.
Run quality control with fluorescent calibration beads every day of use to confirm laser alignment, sensitivity and stability. Full preventive maintenance by a trained engineer, including laser power and optical alignment verification, is normally performed once or twice a year.
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