Analysis devices, kits, and related methods for digital quantification of nucleic acids and other analytes
Provided are devices and methods for effecting processing of samples, including essentially isothermal amplification of nucleic acids, at multiple reaction locations in a single device. In some embodiments, the disclosed devices and methods provide for effecting parallel sample processing in several hundred locations on a single device.
1. A method, comprising:
dispersing a first sample that comprises at least one molecule of interest among a plurality of first areas in both a first substrate and a second substrate, at least one of the plurality of first areas containing one and only one molecule of interest, wherein dispersing said first sample comprises exerting the sample through a first conduit in fluidic communication with the plurality of first areas via a first continuous fluidic path within said first and second substrates:
dispersing a reactant material into a plurality of second areas in both said first substrate and said second substrate; and
effecting pairwise placement of at least some of the plurality of first areas into direct fluidic communication with at least some of the plurality of second areas so as to form closed reaction chambers and contact reactant material with the first sample, wherein the pairwise placement comprises relative motion between the first and second substrates which isolates the plurality of first areas disposed in the first substrate from the plurality of first areas disposed in the second substrate.
2. The method of claim 1 , wherein (a) the first sample is dispersed among the plurality of first areas at essentially the same time among the plurality of first areas, (b) the reactant material is dispersed among the plurality of second areas at essentially the same time among the plurality of second areas, (c) the pairwise placement of the at least some of the plurality of first areas into direct fluidic communication with at least some of the plurality of second areas occurs at essentially the same time among the majority of any pairs formed by first and second areas.
3. The method of claim 1 , wherein the first sample comprises a reagent, and wherein the method further comprises effecting a reaction between the reagent and at least one molecule of interest.
4. The method of claim 3 , wherein the reaction comprises nucleic acid amplification.
5. The method of claim 4 , wherein the amplification is essentially isothermal.
6. The method of claim 4 , further comprising recovering a product of the nucleic acid amplification.
7. The method of claim 3 , wherein the pairwise placement is effected by relative motion of the first and second areas.
8. The method of claim 1 , further comprising effecting a reaction between the contacted reactant material and the first sample.
9. The method of claim 8 , wherein the reactant material comprises an amplification reagent.
10. The method of claim 8 , wherein the reaction comprises nucleic acid amplification of the at least one molecule of interest.
11. The method of claim 10 , wherein the nucleic acid amplification is essentially isothermal.
12. The method of claim 11 , further comprising recovering a product of the nucleic acid amplification.
13. The method of claim 1 , wherein the pairwise placement places at least 10 first areas into direct fluidic communication with at least 10 second areas.
14. The method of claim 13 , wherein the pairwise placement places at least 50 first areas into direct fluidic communication with at least 50 second areas.
15. The method of claim 1 , wherein the pairwise placement is effected by relative motion of the first and second areas.
16. The method of claim 1 , wherein dispersing said reactant material comprises exerting the reactant material through a second conduit in fluidic communication with the plurality of second areas via a second continuous fluidic pathway within said first and second substrates.