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Merck

921548

Sigma-Aldrich

Reaction chamber chip - 20 μl

Fluidic 556, COP

别名:

Microfluidic chip

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About This Item

分類程式碼代碼:
42142600
NACRES:
NA.23

描述

Microfludic chip x1

應用

Chamber chips come in the format of a microscopy slide (75.5 mm x 25.5 mm x 1.5 mm) and are equipped with Mini Luer interfaces. Their key microfluidic elements are reaction chambers of various volumes. Chamber chips are the perfect tool to facilitate reactions, such as amplification of a targeted DNA during qPCR, or to extract target molecules out of a given sample in preparative quantities. These chips can, for example, be used as nucleic acid extraction devices via magnetic beads simply via applying beads and sample and by using an external magnet to hold the beads in place. These procedures can be done completely manually with a pipette – besides the magnet no additional equipment is necessary – or semi-automated with normal peristaltic pumps found in most life science labs.

Reaction chamber chip - 20 μl, Fluidic 556, COP is made of COP (Cyclic olefin polymer) and offers 20μl volume chambers.Reaction chamber chip belong to the simplest, however most versatile, microfluidic devices. From basic reaction chamber to cell culture tool - many experimental setups can be facilitated with this chip family.

Chip Properties:
  • Mini Luer Interface
  • Material: Cyclic olefin polymer (COP)
  • Chamber Volume: 20μl
  • Chamber Depth: 700μm

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Microfluidic-assisted fabrication of carriers for controlled drug delivery.
Santos H A, et al.
Lab on a chip, 17, 1856-1883 (2017)
Recent advances of controlled drug delivery using microfluidic platforms.
Li X, et al.
Advanced Drug Delivery Reviews, 128, 3-28 (2018)
Recent advances of controlled drug delivery usingmicrofluidic platforms.
Li X, et al.
Advanced Drug Delivery Reviews, 128, 3-28 (2018)
Microfluidic-assisted fabrication of carriers for controlled drug delivery.
Santos H A, et al.
Lab on a chip, 17, 1856-1883 (2017)
Dongfei Liu et al.
Lab on a chip, 17(11), 1856-1883 (2017-05-10)
The microfluidic technique has brought unique opportunities toward the full control over the production processes for drug delivery carriers, owing to the miniaturisation of the fluidic environment. In comparison to the conventional batch methods, the microfluidic setup provides a range

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