Product Details
Place of Origin: China
Brand Name: Senova
Certification: CE
Model Number: NovaIncu-250B
Payment & Shipping Terms
Minimum Order Quantity: 1 unit
Price: Available upon request
Packaging Details: plywood case
Delivery Time: 5-20 working days
Payment Terms: T/T
Supply Ability: 100 units
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Model |
NovaIncu BOD-250B |
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Chamber volume (L) |
250 |
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Temp. Control Range |
0℃~70℃ |
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Temperature |
Resolution |
0.1℃ |
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Fluctuation |
±0.5℃ |
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Uniformity |
±1℃ at 37℃ |
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controller |
PID microprocessor control, soft touch, LED display |
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Sensor |
PT100 |
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Timer |
Power-on, power off and working. Timing range: 1min-99hr |
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Material |
Internal |
304 stainless steel |
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External |
Steel (powder coating) |
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Dimensions (WxDxH,cm) |
Internal |
55×50×90 |
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External |
70×75×158 |
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Net Weight(Kg) |
119 |
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Consumption Power(W) |
900 |
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Shelf Size(mm) |
528×480 |
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Shelf Qty(Standard/Max.) |
2/13 |
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Power Supply |
220V/50Hz (Optional: 220V/60Hz, 110V/60Hz) |
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*Notes:
10-segment temperature control program to realize temperature curve program running.
The inflow and outflow air speed is also adjustable.
The classic method for producing monoclonal antibodies—the hybridoma technique—is a multi-step process centered on the CO2 incubator. It begins with immunizing a mouse, then fusing its spleen-derived B-cells with immortal myeloma cells.
The fragile fusion product is plated in a selective medium (HAT medium) in multi-well plates. The incubator’s role is now critical. For 10-14 days, the hybridoma cells must be nurtured at 37°C, 5% CO2, and high humidity. The selective medium is harsh, and the emerging hybridomas are vulnerable. Stable conditions are needed for these cells to proliferate. Researchers screen the supernatant from each well for desired antibody secretion, a process that often involves repeated medium changes and re-incubation. Once positive clones are identified, they are transferred, diluted for cloning, and expanded—all within the protective, stable environment of the incubator.
Any contamination, temperature spike, or pH swing during this period can wipe out a unique, antibody-producing clone that took weeks to generate. Thus, the reliability of the incubator is directly linked to the success rate of obtaining the precious monoclonal antibody lines used in research, diagnostics, and therapy.