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Sticky slide vi0.4 flow chamber

Manufactured by Ibidi

The Sticky-Slide VI0.4 flow chamber is a lab equipment product designed for cell culture applications. It provides a controlled environment for the study of cell behavior and interactions under flow conditions. The product features a transparent, fluidic chamber with a defined geometry to facilitate the observation and analysis of cellular processes.

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2 protocols using sticky slide vi0.4 flow chamber

1

RNA Track Generation using SH-PEG Barriers

Check if the same lab product or an alternative is used in the 5 most similar protocols
To generate RNA tracks, SH-PEG barriers were initially patterned onto the thin gold film using established protocols.34 Briefly, 30 μL of a 1 mM SH-PEG solution in ethanol was applied to a PDMS stamp with 3 μm wide parallel lines spaced at a 3 μm pitch. Next, the SH-PEG solution was dried under a stream of N2 for 1 min and the remaining solution was wicked away. The coated stamp was then brought into contact with the gold film surface for 30 sec. After contact, the stamp was peeled away from the substrate and used to print repeatedly without re-applying additional SH-PEG ink. After patterning the SH-PEG barriers onto the surface, the IBIDI sticky-Slide VI0.4 flow chamber was adhered to the gold slide, and the substrate was prepared as described above in the “Fabrication of RNA monolayers” section. Note that the RNA track preparation protocol used a 6 hr incubation with the DNA anchor solution rather than 12 hrs.
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2

RNA Track Generation using SH-PEG Barriers

Check if the same lab product or an alternative is used in the 5 most similar protocols
To generate RNA tracks, SH-PEG barriers were initially patterned onto the thin gold film using established protocols.34 Briefly, 30 μL of a 1 mM SH-PEG solution in ethanol was applied to a PDMS stamp with 3 μm wide parallel lines spaced at a 3 μm pitch. Next, the SH-PEG solution was dried under a stream of N2 for 1 min and the remaining solution was wicked away. The coated stamp was then brought into contact with the gold film surface for 30 sec. After contact, the stamp was peeled away from the substrate and used to print repeatedly without re-applying additional SH-PEG ink. After patterning the SH-PEG barriers onto the surface, the IBIDI sticky-Slide VI0.4 flow chamber was adhered to the gold slide, and the substrate was prepared as described above in the “Fabrication of RNA monolayers” section. Note that the RNA track preparation protocol used a 6 hr incubation with the DNA anchor solution rather than 12 hrs.
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