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Fluorescence Activated Cell Sorting of Plant Protoplasts
Published on: February 18, 2010
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A new procedure for increasing efficiency of protoplast plating and clone selection.
1International Plant Research Institute, 94070, San Carlos, CA, USA.
Plant Cell Reports
|November 22, 2013
Summary
This study introduces Sea Prep(TM) agarose for plant protoplast culture, improving callus transfer efficiency by 50-fold. This method supports normal shoot formation in potato and tomato cultures.
Area of Science:
- Plant biotechnology
- Plant cell culture
Background:
- Optimizing gelling agents is crucial for efficient plant protoplast culture.
- Traditional methods can limit callus transfer and subsequent development.
Purpose of the Study:
- To evaluate Sea Prep(TM) agarose as a gelling agent for potato and tomato protoplast culture.
- To determine optimal conditions for gelling and liquefaction of the agarose medium.
- To assess the impact of the new method on callus transfer efficiency and shoot formation.
Main Methods:
- Sea Prep(TM) agarose was utilized as the gelling agent.
- Concentration and conditions for gelling and liquefaction were systematically determined.
- Callus transfer efficiency and shoot formation frequency were quantified.
Main Results:
- The optimized Sea Prep(TM) agarose method significantly enhanced callus transfer efficiency, up to 50-fold.
- Protoplast-derived cells exhibited normal shoot formation.
- No reduction in shoot formation frequency was observed compared to control methods.
Conclusions:
- Sea Prep(TM) agarose is an effective gelling agent for potato and tomato protoplast culture.
- The developed method improves efficiency in plant regeneration protocols.
- This technique offers a viable alternative for large-scale plant propagation from protoplasts.
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