Method for carrying out a biochemical protocol in continuous flow in a microreactor
Abstract
Devices and methods for carrying out a chemical or biochemical protocol are disclosed. In one embodiment, the chemical or biochemical protocol is performed by cycling at least one thermal transfer member between at least two temperatures while liquid samples on which the chemical or biochemical protocol is to be performed are continuously moving through at least one temperature regulated zone upon which the at least one thermal transfer member acts. In some embodiments, the device comprises a sample transport member that comprises liquid samples in sample receiving regions. The sample transport member moves the samples continuously through a temperature regulated zone which cycles between at least two temperatures while the liquid samples are moving through a temperature regulated zone on which at least one thermal transfer member acts. In some embodiments, the sample receiving regions comprise wells, hydrophillic films or hydrophillic filaments.
Claims
exact text as granted — not AI-modified1 . A method of performing a chemical or biochemical protocol comprising: cycling at least one thermal transfer member between at least two temperatures while liquid samples on which said chemical or biochemical protocol is to be performed are continuously moving through at least one temperature regulated zone upon which said at least one thermal transfer member acts.
2 . The method of claim 1 , wherein said liquid samples move through the temperature regulated zone in sample receiving regions selected from the group consisting of wells, hydrophilic films and hydrophilic filaments.
3 . The method of claim 1 , wherein said chemical or biochemical protocol comprises adding at least one reagent to the liquid samples.
4 . The method of claim 1 , wherein said cycling between at least two temperatures is repeated 1 to 35 times while said liquid samples are moving through the temperature regulated zone.
5 . The method of claim 1 , wherein said chemical or biochemical protocol comprises a nucleic acid amplification procedure.
6 . The method of claim 1 , wherein said chemical or biochemical protocol is performed on a plurality of liquid samples arranged in parallel.
7 . The method of claim 1 , further comprising detecting the result of said protocol.
8 . The method of claim 1 , wherein said chemical or biochemical protocol comprises determining the identity of at least one polymorphic nucleotide.
9 . A method for carrying out a chemical or biochemical protocol comprising: depositing liquid sample volumes into a plurality of sample receiving regions on at least one mobile sample transport member; and moving the sample transport member along a pathway such that said sample receiving regions move through at least one temperature regulated zone upon which a thermal transfer member acts, wherein said thermal transfer member is capable of cycling between at least two temperatures while said sample receiving regions are moving through said at least one temperature regulated zone.
10 . A device comprising: a substrate comprising regions for receiving liquid samples wherein said liquid samples move along at least one sample pathway; and at least one thermal transfer member which is capable of cycling between at least two temperatures, said at least one thermal transfer member being adapted to bring at least a portion of said sample pathway to said at least two temperatures while a sample is continuously moving along said at least a portion of said sample pathway.
11 . The device of claim 10 , wherein said substrate comprising regions for receiving liquid samples is selected from the group consisting of substrates comprising a plurality of wells, hydrophilic films and hydrophilic filaments.
12 . The device of claim 10 , further comprising at least one reagent supplier.
13 . The device of claim 10 , further comprising a detector for determining the result of said protocol.
14 . A device comprising at least one mobile sample transport member having sample receiving regions thereon and at least one thermal transfer member which is capable of cycling between at least two temperatures, said at least one thermal transfer member being adapted to allow said sample receiving regions to cycle between at least two temperatures while said sample receiving regions are moving through at least one temperature regulated zone upon which said at least one thermal transfer member acts.
15 . The device of claim 14 , further comprising reagent addition members.
16 . The device of claim 14 , wherein the sample receiving regions comprise wells.
17 . The device of claim 16 , wherein the sample receiving regions comprise a plate, having a plurality of wells therein, said wells having a thin film on their bottom surfaces.
18 . The device of claim 17 , wherein the plate is made of a material selected from the group consisting of plastic, silicon and glass.
19 . The device of claim 14 , wherein the sample receiving regions comprise a film.
20 . The device of claim 19 , wherein a surface of the film is sufficiently hydrophilic to allow adherence of individual liquid sample volumes in the form of droplets on the surface.
21 . The device of claim 19 , wherein said film comprises a matrix of hydrophilic areas surrounded by a hydrophobic region, said hydrophilic areas being sufficiently hydrophilic to allow adherence of individual liquid samples in the form of droplets on said hydrophilic areas.
22 . The device of claim 19 , wherein the film is made of a material selected from the group consisting of polyimide, kapton, polycarbonate, PDMS and aluminum.
23 . The device of claim 19 , wherein the film has anisotropic thermal conductivity such that the thermal conductivity through a cross section of the film is greater than the thermal conductivity within a plane of the film.
24 . The device of claim 14 , wherein said sample receiving regions comprise a filament.
25 . The device of claim 24 , wherein the filament is sufficiently hydrophilic to allow adherence of individual liquid sample volumes in the form of droplets on the filament.
26 . The device of claim 25 , wherein the filament is electrically conductive, and the liquid sample volumes are heated by passing electric current through said filament.
27 . The device of claim 14 , further comprising reels, which move said sample transport member along said pathway by frictionally engaging the sample transport member.Join the waitlist — get patent alerts
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