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Merck

Z764116

MicroTissues® 3D Petri Dish® micro-mold Tech Evaluation kit

1 of each mold

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

packaging

pack of 8 ea

manufacturer/tradename

MicroTissues Inc. 8-1

General description

Tech evaluation pack. Mixed pack of eight different autoclavable precision micro-molds to cast 3D Petri Dish, one each of all designs.

This technology evaluation pack contains eight micro-molds, four for use in 12-well plates (Z764000, Z764019, Z764027, Z764035) and four for use in 24-well plates (Z764043, Z764051, Z764078, Z764086). Perfect for exploring the full range of applications.

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.

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Haibo Yang et al.
Advanced healthcare materials, 8(20), e1900929-e1900929 (2019-09-19)
Cellular redox metabolism has emerged as a key tenet in stem cell biology that can profoundly influence the paracrine activity and therapeutic efficacy of mesenchymal stem cells (MSCs). Although the use of materials cues to direct the differentiation of MSCs

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