

Spinner Flask Cell Culture System
转瓶细胞培养系统
- SKU CCS-0002
- Cell Culture Systems
- CE (to be confirmed)
- ISO 9001 manufacturing (to be confirmed)
- IEC 61010-1 safety (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Working volume | 100 mL–3 L |
|---|---|
| Stirring speed | 30–120 rpm |
| Impeller type | Magnetic paddle or angled blade |
| Vessel material | Borosilicate glass or single-use polystyrene |
| Aeration | Headspace, optional sparger |
| Cell density | approx. 1 x 10⁶–5 x 10⁶ cells/mL |
By Lab Manufacturers China Technical TeamLast reviewed Standards: IEC 61010-1, IEC 61010-2-010, IEC 61326-1
What is the Spinner Flask Cell Culture System?
A spinner flask system cultures suspension cells or microcarrier-attached cells in a stirred vessel from 100 mL to several litres, providing a simple and scalable bridge between flask culture and bench-scale bioreactor processes.
What is the Spinner Flask Cell Culture System?
A spinner flask system cultures suspension cells or microcarrier-attached cells in a stirred vessel from 100 mL to several litres, providing a simple and scalable bridge between flask culture and bench-scale bioreactor processes.
Overview
The vessel is a glass or single-use plastic flask with a side arm for sampling and a magnetic impeller driven by an external stirrer. Medium is stirred at 30–120 rpm depending on vessel size and cell sensitivity, keeping suspension cells and microcarriers in motion. Gas exchange occurs at the headspace or through a sparger if fitted, and vessels are placed in a CO2 incubator so that bicarbonate-buffered medium stays at the correct pH. Working volumes of 100 mL to 3 L are typical, and multiple vessels can be run in parallel for process comparison. Because the vessel is simple and inexpensive, spinner culture is widely used for inoculum expansion, for testing microcarrier types and for small-scale production of antibodies and viral vectors.
How does it work?
Scaling cell culture means increasing the surface available for adherent cells or the volume in which suspension cells can grow, while maintaining oxygen, nutrients, pH and temperature. Spinner vessels stir medium with an impeller or a magnetic bar so that cells and microcarriers stay suspended and gas exchange occurs at the surface or through a sparger. Perfusion systems continuously replace medium, keeping nutrient concentrations stable and removing lactate and ammonia, which supports much higher cell densities than batch culture. Hollow fibre bioreactors grow cells on the outside or inside of semi-permeable fibres, supplying oxygen and nutrients by diffusion through the fibre wall and reaching densities of 10⁷–10⁸ cells per millilitre, but sampling cells for counting is difficult. Microfluidic systems keep cells in channels of 100 µm to a few millimetres, giving precise control of flow, gradients and shear at very small volumes. Automated platforms handle flasks or plates robotically, combining incubation, imaging and liquid handling.
What are the key features?
- Glass or single-use vessel with side-arm sampling
- Magnetic impeller driven by an external stirrer
- Stirring speed of 30–120 rpm with low shear
- Headspace aeration or optional sparger for gas exchange
- Working volume of 100 mL to 3 L per vessel
- Parallel vessels for process comparison
What are the technical specifications?
A typical spinner flask cell culture system configuration offers working volume of 100 mL–3 L, stirring speed of 30–120 rpm, impeller type of Magnetic paddle or angled blade, vessel material of Borosilicate glass or single-use polystyrene, aeration of Headspace, optional sparger and cell density of approx. 1 x 10⁶–5 x 10⁶ cells/mL. 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 Spinner Flask Cell Culture System is used in inoculum expansion before bioreactor culture, microcarrier screening and optimisation, antibody production from hybridomas and viral vector production in suspension cells. Across the wider Cell Culture Systems class, laboratories also deploy it for suspension cell expansion for antibody production, microcarrier-based adherent cell culture and cell therapy process development.
Which standards and certifications apply?
Relevant standards and methods include IEC 61010-1, IEC 61010-2-010, IEC 61326-1, ISO 14644-1, USP <1046> and ISO 20387. Certification candidates for this model are CE, ISO 9001 manufacturing and IEC 61010-1 safety; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Start with the oxygen demand: at high density, dissolved oxygen becomes limiting before nutrients do, so sparging, headspace aeration or membrane oxygenation must be matched to the expected cell number. Check that shear from impellers or bubbles does not damage sensitive cells, and reduce agitation or add protective agents where necessary. Perfusion systems need validated tubing, sterile connections and pumps, and the medium feed rate must be tied to measured metabolite concentrations rather than a fixed schedule. Clean and sterilise vessels by autoclaving or single-use assemblies, and verify sterility with a control incubation before inoculating valuable cultures. Record inoculum density, agitation, gas flow, perfusion rate and sampling times so that runs can be compared, and validate the whole culture process against a reference method when results are reported.
How do I select the right Spinner Flask Cell Culture System?
Select a spinner system for intermediate-scale suspension or microcarrier culture, and for experiments that compare microcarrier types, media or agitation rates at bench scale. Specify working volume, stirring range and control, vessel material, aeration method and sampling arrangement.
How does it compare with other Cell Culture Systems variants?
Choose by scale, cell type and how much control the process needs. For a few flasks, an automated platform reduces hands-on time and improves consistency but does not increase capacity much. For suspension cells and microcarrier cultures, spinner vessels are the standard intermediate step, with volume from 100 mL to several litres. When cell density or product titre is the limiting factor, perfusion systems and hollow fibre bioreactors provide far higher densities per unit volume, at the cost of more complex control and harder cell sampling. Microfluidic systems suit mechanistic studies, organ-on-chip models and low-volume screening rather than production. Compare working volume, achievable cell density, oxygenation method, shear levels, perfusion control, sterility of fluid paths, automation level and the availability of validated protocols for your cell type.
Full specifications
| Working volume | 100 mL–3 L |
|---|---|
| Stirring speed | 30–120 rpm |
| Impeller type | Magnetic paddle or angled blade |
| Vessel material | Borosilicate glass or single-use polystyrene |
| Aeration | Headspace, optional sparger |
| Cell density | approx. 1 x 10⁶–5 x 10⁶ cells/mL |
| Microcarrier support | Yes, with intermittent low-speed attachment phase |
| Sampling | Side arm with septum |
| Sterilisation | Autoclave for glass, gamma for single-use |
| Dimensions (W x D x H) | approx. 200 x 200 x 300 mm (1 L vessel) |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Inoculum expansion before bioreactor culture
- Microcarrier screening and optimisation
- Antibody production from hybridomas
- Viral vector production in suspension cells
Key features
- Glass or single-use vessel with side-arm sampling
- Magnetic impeller driven by an external stirrer
- Stirring speed of 30–120 rpm with low shear
- Headspace aeration or optional sparger for gas exchange
- Working volume of 100 mL to 3 L per vessel
- Parallel vessels for process comparison
Frequently asked questions about Spinner Flask Cell Culture System
Start at the lowest speed that keeps cells and microcarriers uniformly suspended, often 30–60 rpm for 100–500 mL vessels, and increase with vessel size. Excessive speed causes shear damage and foam, while too slow allows settling and local nutrient depletion.
Equilibrate and sterilise the microcarriers, then add cells and stir intermittently at low speed for 2–6 hours so cells attach, before increasing to continuous agitation. Bead concentration and surface charge should be matched to the cell type.
Most culture media are bicarbonate buffered and need 5% CO2 to maintain pH 7.4. Placing the vessel in an incubator provides both the gas and the temperature, whereas a heated stirrer alone would not control pH.
Keep oxygen transfer and mixing constant rather than only increasing volume: match the volumetric mass transfer coefficient and specific power input across scales. Nutrient concentration, pH control and inoculation density should also be held constant so that growth rates remain comparable.
When cell density above about 20–30 million cells per millilitre is required, or when a product degrades in the medium. Perfusion keeps nutrients high and metabolites low, increasing volumetric productivity, but needs reliable pumps, sterility and metabolite monitoring.
It provides a very large surface area in a small volume, reaching densities of 10⁷–10⁸ cells per millilitre with gentle, diffusion-based oxygenation. The trade-off is that cells are hard to sample and harvest, so it suits secreted-product processes.
Related models






