922137
Rhombic chamber chip - 120 μl
Fluidic 172, PMMA
Synonyme(s) :
Microfluidic chip
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About This Item
Code UNSPSC :
42142600
Nomenclature NACRES :
NA.23
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Description
Microfludic chip x1
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Application
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.
Rhombic chamber chip - 120 μl, Fluidic 172, PMMA is made of PMMA (Poly(methyl methacrylate)) and offers rhombic chambers with two inlets and two outlets. These chips are versatile tools for various experimental procedures such as sample preparation.
Chip Properties:
Rhombic chamber chip - 120 μl, Fluidic 172, PMMA is made of PMMA (Poly(methyl methacrylate)) and offers rhombic chambers with two inlets and two outlets. These chips are versatile tools for various experimental procedures such as sample preparation.
Chip Properties:
- Orientation: Lengthwise
- Mini Luer Interface
- Material: Poly(methyl methacrylate) (PMMA)
- Chamber Volume: 120μl
- Chamber Depth: 500μm
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Recent advances of controlled drug delivery using microfluidic 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)
Recent advances of controlled drug delivery usingmicrofluidic platforms.
Li X, et al.
Advanced Drug Delivery Reviews, 128, 3-28 (2018)
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