Introduction
Flow Cytometer is equipped with advanced up to 3 lasers (405 nm at 100 mW, 488 nm at 60 mW, and 638 nm at 80 mW) for multi-parameter analysis. The dual threshold setting minimizes debris interference, improving the clarity and reliability of cell analysis. It supports volumetric and microsphere absolute counting methods for precise cell quantification. Our Flow Cytometer is used in research, clinical, and environmental cell analysis.
This flow cytometer is designed to meet the rigorous requirements of modern laboratory operations, ensuring high precision, reliability, and ease of use for various experimental applications.Applications
Flow Cytometer is an advanced instrument used to analyze and quantify physical and chemical characteristics of cells or particles in a fluid. It is widely applied in research laboratories, clinical diagnostics, immunology, hematology, and oncology studies.
Specifications
| Lasers | Up to 3 lasers: 405 nm (100 mW), 488 nm (60 mW), 638 nm (80 mW) |
| Sample Acquisition Rate | Greater than 50,000 events/sec |
| Forward and Side Scatter Resolution | : < 0.45 µm |
| Sensitivity | < 50 ; PE < 30 ; < 30 |
| Fluorescence Linearity | Greater than 0.99 |
| Detector | Detector |
| Detection Particle Range | 0.2 to 50 µm |
| Carryover Rate | Less than 0.1℃ |
| Absolute Count | Compatible with volumetric and microsphere absolute counting |
| Signal Range | Maximum 10⁷ |
| Injection Speed | Low: 15 µL/min; Medium: 30 µL/min; High: 60 µL/min; High 2: 90 µL/min; High 3: 120 µL/min |
| Adjustable Speed Range | 15 to 120 µL/min |
| Threshold Setting | Supports dual thresholds to minimize cell debris |
| Fluorescence Compensation | Automatic online/offline compensation, visual compensation tools |
| Injection Mode | Single tube manual sampling |
| Automatic Sampling | 40-tube auto sampler with single sample mixing |
| Sample Rack | 96-hole plates |
| Software | English interface; supports acquisition and |
| Computer Configuration | i5, 8 GB , 1 TB , 17-inch monitor |
| Dimensions | 760 × 450 × 470 mm |
| Weight | 40 kg |
Features
High-speed acquisition
Submicron resolution detection
Ultra-high sensitivity
Avalanche photodiode detector
Low sample carryover
FAQs
1. How does the Flow Cytometer improve rare cell detection in clinical samples?
The Flow Cytometer enhances the detection of rare populations such as -T cells or minimal residual disease through its ultra-high sensitivity and broad signal range. Its fine forward and side scatter resolution helps distinguish small or dim cell populations from debris. Automatic compensation and dual threshold settings ensure clean separation of rare events, even in complex clinical matrices. The detector boosts signal precision and reduces background noise. Together, these features facilitate reliable identification of rare cells for accurate diagnostics and monitoring.
2. Can the Flow Cytometer streamline high-throughput immunophenotyping workflows?
Yes, the Flow Cytometer is built for high-throughput workflows, it offers an autosampler with a 40-tube capacity and 96-well plate support, reducing manual handling. Adjustable injection speeds allow optimization between throughput and data quality. Automated fluorescence compensation simplifies multicolor panel setup. The English interface enables simultaneous data acquisition and analysis, yielding rapid results. Its compact design saves bench space, ideal for shared core facilities or clinical labs seeking efficient immunophenotyping.
3. In what ways is the Flow Cytometer suitable for stem cell and -T studies?
Flow Cytometer is highly suitable for stem cell and -T research, offering sensitive detection and broad dynamic range required for rare and heterogeneous populations. Its low carryover and dual thresholds maintain sample integrity across sequential runs. Absolute counting via volumetric or microsphere methods enables precise cell quantification in therapeutic preparations. The inclusion of three excitation lasers supports multicolor panels for discriminating diverse cell subsets, and its detector ensures reliable signal capture across low and high expression levels.
4. How does the Flow Cytometer ensure data reproducibility in environmental monitoring applications?
Flow Cytometer delivers reproducible data by offering robust particle detection its detection range extends from bacteria and viruses to algae. Dual thresholds effectively exclude debris common in environmental samples. With minimal carryover rates, sequential runs remain uncontaminated. Absolute counting capabilities enable accurate quantification of microorganisms. Adjustable flow rates and a wide dynamic signal range allow flexibility when handling variable sample types. Overall, it supports reliable environmental monitoring and pathogen enumeration.
5. What makes the Flow Cytometer advantageous for immunology-based assays like T-cell proliferation or cytokine detection?
Flow Cytometer is ideal for immunology assays due to its multicolor detection capability across three lasers and automated compensation tools. High sensitivity captures subtle fluorescence differences important in -based proliferation or low-level cytokine expression. detection ensures clarity even with dim markers. The software enables simultaneous acquisition and data analysis, streamlining workflow. Adjustable speeds and dual thresholds help handle variable sample types while maintaining clean data. These features facilitate accurate characterization of complex immune cell subsets.
6. How can the Flow Cytometer help with consistent absolute counting in hematology analysis?
The Flow Cytometer delivers consistent absolute counting using both volumetric and microsphere methods, giving flexibility for different workflows. Its volumetric measurement ensures accuracy when bead supplies are limited, while microspheres provide external standards. Low carryover preserves sample integrity across consecutive runs. Adjustable injection speeds accommodate varying cell concentrations. With its broad signal range and high resolution, both low-abundance and high-expression cell populations can be accurately enumerated, aiding precise hematology profiling.
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