US2014099675A1PendingUtilityA1
Reusable pcr amplification system and method
Est. expiryDec 16, 2025(expired)· nominal 20-yr term from priority
Inventors:Venumadhav KorampallyShubhra GangopadhyayKeshab GangopadhyaySheila GrantSteven B. KleiboekerShantanu BhattacharyaYuanfang Gao
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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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-modifiedWhat 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.Cited by (0)
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