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物質
spherical
無菌性
sterile; autoclaved
特徴
lid: no
honeycomb diam. 3.4 mm
包装
pack of 6 ea
メーカー／製品名
MicroTissues Inc. 24-H
容量
20 μL
詳細
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.
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.
- 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
法的情報
3D Petri Dish is a registered trademark of MicroTissues Inc.
MicroTissues is a registered trademark of MicroTissues Inc.
試験成績書（COA）
製品のロット番号・バッチ番号を入力して、試験成績書（COA） を検索できます。ロット番号・バッチ番号は、製品ラベルに「Lot」または「Batch」に続いて記載されています。
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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