Silicone-coated Dish
Silicone-coated Dish - Related Videos
03:53
Preparation of Collagen-Coated Compartmented Culture Dishes for Neuronal Cell Culture
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2025
This video demonstrates constructing a three-compartment cell culture system using collagen and non-reactive grease. This system is used to observe interactions between glioma cells and axons in real-time.
06:47
Production of Cardiac Extracellular Matrix from Adult Human Fibroblasts for Culture Dish Coating
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Cited by 1 •
2024
Fibroblasts isolated from the adult human heart were cultured to confluence on gelatin-coated dishes to produce the myocardium-specific extracellular matrix. After decellularization, this substrate can be used for the culture and study of other cardiac cells and cell-matrix interactions.
06:10
A 3D-Printed Silicone-Coated Device to Model Catheter-Associated Urinary Tract Infection
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2025
Source:Ocean E. Clarke1, Romy A. Dop1, Tom Hasell1, Joanne L. Fothergill1, Daniel R. Neill21University of Liverpool, 2 University of DundeeThis video demonstrates the use of a 3D-printed, silicone-coated device that mimics the inner surface of urinary catheters to simulate catheter-associated urinary tract infection.
05:02
Growth of Gold Dendritic Nanoforests on Titanium Nitride-coated Silicon Substrates
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Cited by 5 •
2019
This study presents a feasible procedure for synthesizing gold dendritic nanoforests on titanium nitride/silicon substrates. The thickness of gold dendritic nanoforests increases linearly within 15 min of a synthesis reaction.
03:57
Microtiter Dish Biofilm Formation Assay
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Cited by 2235 •
2011
The assay describes a rapid means to measure early biofilm formation in bacteria and fungi. This method uses a microtiter plate as the substratum for microbial biofilm formation, and the biofilm is visualized using crystal violet strain. The assay provides either a qualitative or quantitative assay for early biofilm formation.
FAQs
The cured silicone layer creates a water-repelling, chemically resistant interface that limits adsorption of biological material to the vessel surface. Because specimens are less likely to bind tightly, researchers can reposition or retrieve them with reduced force. This surface behavior is especially valuable when handling delicate cells, tissues, embryos, or other specimens whose morphology could be altered by aggressive manipulation.
Low adhesion reduces the tendency of specimens to remain fixed to the dish during positioning, transfer, or recovery. That minimizes mechanical disruption and helps limit sample loss when researchers move material between steps. In practical terms, the dish supports controlled manipulation while preserving the specimen's location and visible structure for subsequent biological work.
A silicone-coated dish is selected when researchers need specimens to remain movable rather than firmly anchored to the vessel. Its low-adhesion behavior contrasts with attachment-oriented surfaces, which hold cells or tissues in place for growth or observation. The distinction determines whether the priority is secure adhesion or easier positioning, recovery, and transfer with less physical disturbance.
Researchers place the specimen in the dish, use the smooth low-adhesion surface to position or manipulate it, and then recover or transfer it when the operation is complete. The same workspace can support handling, microdissection, or selected culture protocols. Its main procedural benefit is maintaining access to the specimen while reducing attachment-related resistance during each step.
They are useful in cell biology, developmental biology, microdissection, and embryo handling, particularly when clean transfer or preservation of specimen morphology is important. Researchers may choose them for procedures that require repeated positioning, manipulation, or recovery. The dish is therefore suited to workflows where minimizing sample loss and mechanical disruption improves handling quality.
By limiting attachment to the working surface, the dish can help researchers recover specimens more completely and maintain their observable morphology during handling. These advantages support accurate positioning and controlled transfer of cells, tissues, embryos, and other biological materials. In developmental and cellular studies, preserving specimen form can make subsequent examination or manipulation more reliable.