Z764000
MicroTissues® 3D Petri Dish® micro-mold spheroids
size S, 16 x 16 array, fits 12 well plates
Synonym(s):
3D, 3D Cell Culture
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About This Item
UNSPSC Code:
41121812
NACRES:
NB.14
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material
spherical
size
S
sterility
sterile; autoclaved
feature
lid: no
16 x 16 array
packaging
pack of 6 ea
manufacturer/tradename
MicroTissues Inc. 12-256
volume
190 μL
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General description
Six autoclavable precision micro-molds to cast 3D Petri Dish for forming small spheroids. 3D Petri Dish for use in 12-well plate. Each micro-mold forms 256 circular recesses in a 16 x 16 array.
- Nominal dimensions of each 3D culture recess: diam. 300 μm x D 800 μm
- Micro-molds also form single chamber for cell seeding
When the gelled agarose is removed from the micro-mold, it is transferred to a standard 12 well or 24 well tissue culture dish and equilibrated with cell culture medium.
Since the agarose is transparent, the spheroids or microtissues that form at the bottom of each agarose micro-well can be easily viewed using a standard inverted microscope using phase contrast, bright field or fluorescence microscopy.
Since the agarose is transparent, the spheroids or microtissues that form at the bottom of each agarose micro-well can be easily viewed using a standard inverted microscope using phase contrast, bright field or fluorescence microscopy.
- The micro-molds are reusable up to 12 times and can be sterilized via a standard steam autoclave (30 min, dry cycle)
- The micro-molds should be stored in a covered container to maintain sterility and to avoid collecting dust or fibres on their small features
- Any microscope with sufficient magnification and resolution functions for cell based views or images will be suitable for use with the 3D Petri Dish products
Legal Information
3D Petri Dish is a registered trademark of MicroTissues Inc.
MicroTissues is a registered trademark of MicroTissues Inc.
Certificates of Analysis (COA)
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Minjae Kim et al.
Journal of cell science, 132(19) (2019-09-08)
Cultured rat primitive extraembryonic endoderm (pXEN) cells easily form free-floating multicellular vesicles de novo, exemplifying a poorly studied type of morphogenesis. Here, we reveal the underlying mechanism and the identity of the vesicles. We resolve the morphogenesis into vacuolization, vesiculation
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