

Cell Cycle and Apoptosis Analyzer
细胞周期与凋亡分析仪
- SKU CAN-0005
- Cell Analyzers
- CE (to be confirmed)
- ISO 9001 manufacturing (to be confirmed)
- IEC 61010-1 safety (to be confirmed)
- IEC 60825-1 laser safety (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Laser | 488 nm, 20–50 mW |
|---|---|
| Detectors | 2–4 fluorescence channels plus scatter |
| Sample volume | 100–500 µL |
| Acquisition rate | up to 10,000 events per second |
| Cell cycle output | G0/G1, S and G2/M percentages with CV |
| Apoptosis assays | Annexin V, caspase activity, membrane potential |
By Lab Manufacturers China Technical TeamLast reviewed Standards: IEC 60825-1, IEC 61010-1, ISO 15189
What is the Cell Cycle and Apoptosis Analyzer?
A dedicated cell cycle and apoptosis analyzer measures DNA content and apoptotic markers with a fixed optical configuration, quantifying G0/G1, S and G2/M fractions and Annexin V or caspase signals in a simplified workflow.
What is the Cell Cycle and Apoptosis Analyzer?
A dedicated cell cycle and apoptosis analyzer measures DNA content and apoptotic markers with a fixed optical configuration, quantifying G0/G1, S and G2/M fractions and Annexin V or caspase signals in a simplified workflow.
Overview
The instrument uses a 488 nm laser and a small number of detectors optimised for propidium iodide or DAPI DNA staining and for fluorescein-labelled Annexin V or caspase substrates. Permeabilised or fixed cells stained for DNA are analysed for total fluorescence per cell, which corresponds to DNA content, and the software fits the resulting histogram to report the percentage of cells in G0/G1, S and G2/M phases along with the coefficient of variation of the G0/G1 peak. Apoptosis assays measure externalised phosphatidylserine with Annexin V and membrane integrity with a viability dye, distinguishing early apoptotic, late apoptotic and necrotic cells. The simplified configuration reduces setup time and training needs, but excludes the larger panels that a general-purpose cytometer supports.
How does it work?
Flow-based cell analyzers suspend cells in a sheath fluid that hydrodynamically focuses them into a single file. Each cell passes one or more laser beams, and detectors record forward scatter, which relates to size, side scatter, which relates to granularity, and fluorescence from labelled antibodies or reporter proteins. Thousands of cells are measured per second, so rare populations can be quantified with statistical confidence. Spectral analyzers capture the full emission spectrum for each event and unmix overlapping dyes computationally, allowing larger panels. Imaging cytometers capture a brightfield and fluorescence image of each cell in flow, adding morphology and localisation information. Metabolic analyzers measure oxygen consumption and extracellular acidification in a plate by repeatedly sampling the medium above the cells, giving a readout of oxidative phosphorylation and glycolysis. Dedicated cell cycle analyzers measure DNA content and apoptosis markers with fixed panels.
What are the key features?
- 488 nm laser with detectors optimised for DNA dyes
- Automatic cell cycle fitting reporting G0/G1, S and G2/M fractions
- Annexin V and viability dye combination for apoptosis staging
- Caspase substrate and mitochondrial membrane potential assays
- Simple workflow with dedicated reagent kits
- Histogram and dot plot reports exported to PDF or CSV
What are the technical specifications?
A typical cell cycle and apoptosis analyzer configuration offers laser of 488 nm, 20–50 mW, detectors of 2–4 fluorescence channels plus scatter, sample volume of 100–500 µL, acquisition rate of up to 10,000 events per second, cell cycle output of G0/G1, S and G2/M percentages with CV and apoptosis assays of Annexin V, caspase activity, membrane potential. 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 Cell Cycle and Apoptosis Analyzer is used in drug-induced cell cycle arrest studies, apoptosis and cytotoxicity testing, proliferation and DNA content analysis and cell therapy potency assay development. Across the wider Cell Analyzers class, laboratories also deploy it for immunophenotyping of cell populations, cell cycle and apoptosis analysis and cell therapy product characterisation.
Which standards and certifications apply?
Relevant standards and methods include IEC 60825-1, IEC 61010-1, ISO 15189, CLSI H42, USP <1046> and ISO 17025. Certification candidates for this model are CE, ISO 9001 manufacturing, IEC 61010-1 safety and IEC 60825-1 laser safety; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Standardise sample preparation, since cell number, staining volume, incubation time and wash steps all shift signal intensity. Include single-stain compensation controls and an unstained control in every experiment, and run reference beads for instrument setup and daily quality control. Keep sheath fluid and waste containers at the correct levels, and follow the manufacturer's cleaning procedure to limit carry-over below 1%. Lasers fall under IEC 60825-1, so protective covers and interlocks must remain functional and staff should be trained. Fixed cells for DNA content analysis need correct fixation and RNase treatment. For regulated work, document compensation, gating strategy, acquisition settings and software version, and retain raw FCS files so that analyses can be reproduced.
How do I select the right Cell Cycle and Apoptosis Analyzer?
Select a dedicated analyser for routine cell cycle and apoptosis testing where simple workflows and repeatable histogram fitting matter more than panel flexibility. Specify detector count, supported assays, cell number requirements and the reporting format required for your records.
How does it compare with other Cell Analyzers variants?
Define the panel before specifying hardware. Count how many fluorophores must be measured simultaneously, then check that the laser and detector configuration can resolve them, including compensation or spectral unmixing capability. Conventional benchtop systems suit routine 4–10 colour panels for immunophenotyping and cell cycle work. Spectral systems are appropriate when panels exceed about 12 colours or when autofluorescence varies between samples. Imaging cytometry answers questions involving cell shape, internalisation or cell-cell contact that scatter and fluorescence alone cannot resolve. Metabolic analysis addresses a different question entirely: how cells produce energy, and how they respond to inhibitors or genetic changes. All platforms need consistent sample preparation, validated compensation or unmixing controls, and documented acquisition settings so that results remain comparable between runs.
Full specifications
| Laser | 488 nm, 20–50 mW |
|---|---|
| Detectors | 2–4 fluorescence channels plus scatter |
| Sample volume | 100–500 µL |
| Acquisition rate | up to 10,000 events per second |
| Cell cycle output | G0/G1, S and G2/M percentages with CV |
| Apoptosis assays | Annexin V, caspase activity, membrane potential |
| Cells per test | approx. 1 x 10⁵–1 x 10⁶ |
| Carry-over | below 1% with wash cycle |
| Report output | PDF histogram and statistics report |
| Dimensions (W x D x H) | approx. 400 x 450 x 500 mm |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Drug-induced cell cycle arrest studies
- Apoptosis and cytotoxicity testing
- Proliferation and DNA content analysis
- Cell therapy potency assay development
Key features
- 488 nm laser with detectors optimised for DNA dyes
- Automatic cell cycle fitting reporting G0/G1, S and G2/M fractions
- Annexin V and viability dye combination for apoptosis staging
- Caspase substrate and mitochondrial membrane potential assays
- Simple workflow with dedicated reagent kits
- Histogram and dot plot reports exported to PDF or CSV
Frequently asked questions about Cell Cycle and Apoptosis Analyzer
Cells are stained for DNA and the fluorescence histogram is fitted with a mathematical model that estimates the G0/G1 and G2/M peaks plus the S-phase region between them. Debris and aggregate correction options improve accuracy.
Cells must be fixed and permeabilised so the dye reaches DNA, treated with RNase when propidium iodide is used, and kept as single cells to avoid doublet artefacts. Inconsistent fixation shifts peak positions and distorts phase percentages.
Annexin V binds externalised phosphatidylserine on apoptotic cells, while a viability dye such as propidium iodide enters only cells with damaged membranes. Annexin-positive and dye-negative cells are early apoptotic, double-positive cells are late apoptotic or necrotic.
Conventional benchtop analysers typically resolve 4–12 fluorescence colours using two to four lasers, while spectral analysers support panels above 12 colours by capturing full emission spectra. Practical panel size is limited by dye overlap and by the number of available detectors.
It measures oxygen consumption rate and extracellular acidification rate in a multi-well plate while injecting compounds. These readouts reflect mitochondrial respiration and glycolysis, allowing cells to be compared under different nutrients, inhibitors or genetic backgrounds.
Fluorophores emit across a range of wavelengths, so signal from one dye appears in detectors assigned to others. Single-stain controls allow the software to calculate and subtract that spillover, keeping populations in their correct quadrants and preventing false positive calls.
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