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  1. Journal of Visualized Experiments
  2. Year: 2007
  3. Year: 2007 Issue: 9
  4. Non-plasma bonding of PDMS for inexpensive fabrication of microfluidic devices.
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Year: 2007
Year: 2007 Issue: 10
Year: 2007 Issue: 9
Transplantation of pancreatic islets into the kidney capsule of diabetic mice.
RNA extraction from neuroprecursor cells using the bio-rad total RNA kit.
Understanding cerebellar pattern formation.
In ovo electroporations of HH stage 10 chicken embryos.
Isolation of CD4+ T cells from mouse lymph nodes using Miltenyi MACS purification.
Non-plasma bonding of PDMS for inexpensive fabrication of microfluidic devices.
BioMEMS: forging new collaborations between biologists and engineers.
Year: 2007 Issue: 8
Year: 2007 Issue: 7
Year: 2007 Issue: 6
Year: 2007 Issue: 5
Year: 2007 Issue: 4
Year: 2007 Issue: 3
Year: 2007 Issue: 2
Year: 2006

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Non-plasma bonding of PDMS for inexpensive fabrication of microfluidic devices.

Content Provider World Health Organization (WHO)-Global Index Medicus
Author Harris, Joseph Lee, Hyuna Vahidi, Behrad Tu, Cristina Cribbs, David Cotman, Carl Jeon, Noo Li
Description Country affiliation: United States Author Affiliation: Harris J ( Department of Biomedical Engineering, University of California, Irvine, CA, USA. jwharris7@gmail.com)
Abstract In this video, we demonstrate how to use the neuron microfluidic device without plasma bonding. In some cases it may be desirable to reversibly bond devices to the Corning No. 1 cover glass. This could be due, perhaps, to a plasma cleaner not being available. In other instances, it may be desirable to remove the device from the glass after the culturing of neurons for certain types of microscopy or for immunostaining, though it is not necessary to remove the device for immunostaining since the neurons can be stained in the device. Some researchers, however, still prefer to remove the device. In this case, reversible bonding of the device to the cover glass makes that possible. There are some disadvantages to non-plasma bonding of the devices in that not as tight of a seal is formed. In some cases axons may grow under the grooves rather than through them. Also, because the glass and PDMS are hydrophobic, liquids do not readily enter the device making it necessary at times to force media and other reagents into the device. Liquids will enter the device via capillary action, but it takes significantly longer as compared to devices that have been plasma bonded. The plasma cleaner creates temporary hydrophilic charges on the glass and device that facilitate the flow of liquids through the device after bonding within seconds. For non-plasma bound devices, liquid flow through the devices takes several minutes. It is also important to note that the devices to be used with non-plasma bonding need to be sterilized first, whereas plasma treated devices do not need to be sterilized prior to use because the plasma cleaner will sterilize them.
File Format HTM / HTML
e-ISSN 1940087X
DOI 10.3791/410
Journal Journal of Visualized Experiments
Issue Number 9
Language English
Publisher MyJove Corp.
Publisher Date 2007-01-01
Publisher Place United States
Access Restriction Open
Subject Keyword Discipline Physical Sciences Discipline Life Sciences Discipline Medicine Dimethylpolysiloxanes Microfluidic Analytical Techniques Instrumentation Neurons Cytology Nylons Animals Video-audio Media
Content Type Text
Resource Type Article
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