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Merck

Z764086

MicroTissues® 3D Petri Dish® micro-mold honeycombs

makes honeycomb-shaped microtissues, fits 24 well plates, honeycomb diam. 3.4 mm

Sinónimos:

3D, 3D Cell Culture

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About This Item

UNSPSC Code:
41121812
NACRES:
NB.14

material

spherical

sterility

sterile; autoclaved

feature

lid: no
honeycomb diam. 3.4 mm

packaging

pack of 6 ea

manufacturer/tradename

MicroTissues Inc. 24-H

volume

20 μL

General description

Six autoclavable precision micro-molds to cast 3D Petri Dish for forming honeycomb shaped microtissue. 3D Petri Dish for use in 24-well plate. Each micro-mold forms 1 honeycomb shaped recess.

  • Nominal dimensions of each 3D culture recess: maximum size 3.4 mm
  • Peg diam. 600 μm
  • Trough W 400 μm x D 700 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.
  • 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.

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Los clientes también vieron

B R Desroches et al.
American journal of physiology. Heart and circulatory physiology, 302(10), H2031-H2042 (2012-03-20)
To bridge the gap between two-dimensional cell culture and tissue, various three-dimensional (3-D) cell culture approaches have been developed for the investigation of cardiac myocytes (CMs) and cardiac fibroblasts (CFs). However, several limitations still exist. This study was designed to

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