Genome Research cityscape

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Yuen, P. K.
Right arrow Articles by Wilding, P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Yuen, P. K.
Right arrow Articles by Wilding, P.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

Vol. 11, Issue 3, 405-412, March 2001

LETTER
Microchip Module for Blood Sample Preparation and Nucleic Acid Amplification Reactions

Po Ki Yuen,1,4 Larry J. Kricka,1,5 Paolo Fortina,2 Nicholas J. Panaro,1 Taku Sakazume,1,2,3 and Peter Wilding1

1 Departments of Pathology and Laboratory Medicine, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA; 2 Department of Pediatrics, University of Pennsylvania School of Medicine and The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA; 3 Hitachi Ltd., Instrument Division, Hitachinaka-shi, Ibaraki-ken, 312-8504, Japan

A computer numerical control-machined plexiglas-based microchip module was designed and constructed for the integration of blood sample preparation and nucleic acid amplification reactions. The microchip module is comprised of a custom-made heater-cooler for thermal cycling, a series of 254 µm × 254 µm microchannels for transporting human whole blood and reagents in and out of an 8-9 µL dual-purpose (cell isolation and PCR) glass-silicon microchip. White blood cells were first isolated from a small volume of human whole blood (<3 µL) in an integrated cell isolation-PCR microchip containing a series of 3.5-µm feature-sized "weir-type" filters, formed by an etched silicon dam spanning the flow chamber. A genomic target, a region in the human coagulation Factor V gene (226-bp), was subsequently directly amplified by microchip-based PCR on DNA released from white blood cells isolated on the filter section of the microchip mounted onto the microchip module. The microchip module provides a convenient means to simplify nucleic acid analyses by integrating two key steps in genetic testing procedures, cell isolation and PCR and promises to be adaptable for additional types of integrated assays.


4 Present address: Corning Incorporated, Biochemistry Core Technology, Science & Technology, SP-FR-01, Corning, NY 14831-0001, USA.

5 Corresponding author.


11:405-412 ©2001 by Cold Spring Harbor Laboratory Press  ISSN 1088-9051/01 $5.00

Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
Genome Res.Home page
T. Kajiyama, Y. Miyahara, L. J. Kricka, P. Wilding, D. J. Graves, S. Surrey, and P. Fortina
Genotyping on a Thermal Gradient DNA Chip
Genome Res., March 1, 2003; 13(3): 467 - 475.
[Abstract] [Full Text] [PDF]




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
Genes Dev. Learn. Mem.
Protein Science RNA Genome Res.