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ibidi Labware | Microscopy
Live Cell Imaging | ibidi Stage Top Incubators
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µ-Slide 8 Well high
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ibidi Reagents | Collagen
How do I prepare a 3D gel using the ibidi Collagen Type I solution?
Why does my collagen gel become turbid after polymerization?
Does the temperature play a role in the initiation of collagen polymerization?
My collagen 3D gel looks very inhomogeneous. What is the reason for that?
Can I pipet the collagen gel after polymerization?
Why are the ibidi Collagens Type I non-pepsinized?
What can I do when my cells do not adhere or grow on a collagen hydrogel?
Can the viscosity of the ibidi Collagen Type I solution be different from lot to lot?
Why does the 10 mg/ml solution of the ibidi Collagen Type I, Rat Tail have such a high viscosity?
My cells need pH 6.0 in the 3D collagen matrix. Can the gel be adjusted to a pH lower (or higher) than the 7.2–7.4 that is recommended in the instructions?
How can I retrieve/harvest cells or spheroids from a collagen hydrogel?
Can the ibidi Mounting Medium be used with the Immunofluorescence Chamber Slides 3 Well | 8 Well | 12 Well Chamber, removable?
Can water immersion objectives be used with the ibidi Mounting Medium (#50001)?
The ibidi Mounting Medium with DAPI is too bright, what can I do?
How can ibidi Anti-Evaporation Oil be sterilized?
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