US2019169676A1PendingUtilityA1

Thermal reaction device and method for using the same

69
Assignee: FLUIDIGM CORPPriority: Apr 3, 2003Filed: Oct 2, 2018Published: Jun 6, 2019
Est. expiryApr 3, 2023(expired)· nominal 20-yr term from priority
B01L 7/52C12Q 1/68B01L 2200/147B01L 3/50273B01L 3/5027B01L 2300/0816B01L 3/502707C12Q 1/686B01L 3/5025B01L 3/502738G01N 27/453B01L 2200/0642B01L 3/502715B01L 2300/0636B01L 2200/142B01L 2300/0819B01L 3/0248B01L 2300/1805B01L 2400/0638B01L 2300/0861B01L 2400/0481B01L 2400/0655B01L 2300/123B01L 2400/0487B01L 2300/0867B01L 2300/0864B01L 2200/10B01L 2300/0874B01L 2400/06B01L 2300/06
69
PatentIndex Score
0
Cited by
0
References
0
Claims

Abstract

A method for carrying out nucleic acid amplification reactions using a microfluidic device is described. Amplification primers and other amplification reagents are deposited at a plurality of reaction sites in the device, a sample solution containing amplifiable polynucleotides is introduced into the reaction sites, and amplification is carried out.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method for performing an analysis of a sample comprising the steps of:
 providing a microfluidic device having a channel dimension between 0.1 and 1000 μm, and having at least one sample channel, wherein the sample channel is able to be partitioned into a plurality of separate chambers by one or more valves, said valves being formed in said microfluidic device such that a deflectable membrane(s) can be deflected into said sample channel to partition said sample channel into one or more separate chambers,   introducing a sample having at least one amplifiable target therein into said sample chamber,   actuating said valves to form said separate chambers so that said at least one amplifiable target is isolated into at least one chamber,   conducting an amplification step or steps,   detecting whether amplification occurred in one or more chambers to determine the quantity or presence of the amplifiable target within the sample.

Cited by (0)

No later patents cite this yet.

References (0)

No backward citations on record.