US2014099675A1PendingUtilityA1

Reusable pcr amplification system and method

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Assignee: UNIV MISSOURIPriority: Dec 16, 2005Filed: Sep 9, 2013Published: Apr 10, 2014
Est. expiryDec 16, 2025(expired)· nominal 20-yr term from priority
B01L 2400/0481B01L 2300/0816B01L 2400/0421B01L 3/5027B01L 2300/123B01L 2300/0867B01L 3/502707C12Q 1/6844C12Q 1/686B01L 2300/1827C12P 19/34B01L 2200/12B01L 7/52
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Claims

Abstract

A DNA amplification device utilizing a polydimethylsiloxane (PDMS) and silicon substrate coated with spin-on glass (SOG) is provided. This PDMS layer is irreversibly bonded to the SOG layer of the silicon substrate using oxygen plasma. The amplification device is an inexpensive, microfluidic device, which can be utilized as a portable thermo-cycler to perform PCR amplification of DNA in the field.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method for amplifying a DNA sample, comprising:
 providing a reusable amplification device, the inner surfaces of the amplification device consisting of a polydimethylsiloxane layer bonded to a spin-on glass layer;   introducing a first DNA sample into the amplification device;   replicating the first DNA sample;   extracting the replicated first DNA sample;   washing the amplification device;   introducing a second DNA sample; and   replicating the second DNA sample, wherein there is minimal or no contamination of the second DNA sample with the first DNA sample.   
     
     
         2 . The method of  claim 1 , wherein the spin-on glass comprises methyl silsesquioxane. 
     
     
         3 . The method of  claim 1 , wherein the reusable amplification device comprises one or more peristaltic pumps for delivering a wash buffer solution for washing the amplification device. 
     
     
         4 . The method of  claim 1 , wherein the inner surfaces of the amplification device do not bind strongly with DNA.

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