Frequently Asked Questions (FAQ)
All users of bioreactor systems have questions, sooner or later. This is due not only to the technical aspects of the product, but also because of the many different ways to analyze and influence biological processes.
The FAQs listed here represent a selection of the questions that we receive most often. We look forward to even more. It's these questions that help us better understand the people who use our products and what their needs are. They also tell us that you use and have an interest in our products. Should you have a question that is not answered to your satisfaction here, don't hesitate to get in touch with us!
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Questions about DASGIP Technology
- What are typical applications for DASGIP Bioreactor Systems?
- How many bioreactors are operated simultaneously using DASGIP?
- How much space does a 4-fold bioreactor system require?
- How many parameters can I control using DASGIP System?
- How many parameters can be displayed in a process overview?
- Do I need programming skills to automate my process?
- Can I change triggers, profiles, cascades and scripts online?
- How difficult is it to modify a DASGIP System subsequently?
- How many speed controlled pumps do the DASGIP Reactors feature?
- Which temperature range can be controlled in a DASGIP Bioreactor?
- How many mass flow sensors are available?
- What is the benefit of the off-gas-analysis?
- How many ports do DASGIP reactors feature?
- Which working volumes are available using DASGIP Control System?
- How is the reactor protected against overheating?
- How are DASGIP vessels agitated?
- Can I integrate DASGIP with Historians & Supervisory Control?
- How can I harness data generated by Parallel Bioreactor System?
- Can I get remote access to a running process outside my lab?
- Are there any alarms in case of critical deviation?
- Why do I need calibration data sheets for the DASGIP BioLector?
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Technical Questions
- I can not log-in into DASGIP Control: what is the reason?
- Can you help me with my controller loop parameters?
- What can I do against the pH drift during longer experiments?
- How to calibrate a pH probe?
- How strong is the influence of temperature for my pH calibration?
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What is a cascade in dissolved oxygen (DO) control?
The control of dissolved oxygen inside a DASGIP bioreactor bases on a control loop adjusting several set-points of the so called “actors”. Potential ways to increase oxygen transfer are oxygen enrichment, gas flow and/or agitation adjustment. Usually the control strategy is to change the actors’ set-points sequentially as defined in the cascade. For example in cell cultivations agitation usually is not changed for shear reasons and the gas flow might be kept minimized if the media tends to foam. So the usual set-up of the DO-cascade might be depending mainly on oxygen enrichment from air to pure oxygen and then shifting to a slight flow adjustment. This may be completely different when working with robust microorganisms and high cell densities. Here, a higher agitation often is required to prevent from oxygen limitations, followed by increased gas flow and then by oxygen enrichment.
The DASGIP system supports multiple gassing strategies and specific agitation modules providing various ways of DO control. For example mass flow controllers in the gas mixing module allow both precise oxygen enrichment and flow adjustment.
Using DASGIP Control software all three cascade parameters can be defined independently and simultaneously for all included batches. This allows automated DO control meeting individual demands. Unlike other bioreactor control systems the DASGIP system additionally features a unique online visualization and online changes of the DO cascade. This helps users to adapt and optimize DO control at any time during the process run.
Follow the link to find a screenshot of the online editable DO cascade.
For more information contact service@dasgip.de or call +49-700-DASGIP-AG/+49-700-327447-24 - What is 100%DO and what is the difference to 100V% oxygen?
- What calibration parameters do you recommend for a DO probe?
- Is it possible to receive a negative OTR in off-gas measurement?
- What are typical process variables to be controlled by triggers?
- How reliable are off-gas data when working at benchtop scale?
- Is it possible to feed continuously even at very low feed rates?
- How to clean Polytetrafluorethylen (PTFE) components?
- How to clean metal sparger?
- How to clean glas sparger?
- How to clean stainless steel components?
- Do stainless steel components bear any risk of corrosion?
- Is it possible to automatically control the foam in DASGIP vessels?
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General Questions
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Glossary
