Fluid delivery methods
US-2024408593-A1 · Dec 12, 2024 · US
US10112195B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10112195-B2 |
| Application number | US-201414907844-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 11, 2014 |
| Priority date | Jul 31, 2013 |
| Publication date | Oct 30, 2018 |
| Grant date | Oct 30, 2018 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Provided is a flow cell for nucleic acid analysis used for a sequence reaction with photocleavable nucleotides where an efficiency of the photocleaving reaction can be enhanced and noise upon florescence detection can be mitigated, thereby improving the accuracy of sequencing, shortening a runtime, and extending a read length. The flow cell for nucleic acid analysis includes a first substrate 101 provided with an optical filter 102 reflecting first light for changing a chemical structure of a substance in a flow passage, a hollow sheet 103 having a hollow portion for forming the flow passage, and a second substrate 105 transmitting the first light, in which the first substrate, the hollow sheet, and the second substrate are attached to each other.
Opening claim text (preview).
The invention claimed is: 1. A flow cell for nucleic acid analysis, comprising: a first substrate provided with an optical filter which reflects a first light for carrying out a photo-cleaving reaction with a nucleotide having an intramolecular fluorescent molecule via a photocleavable linker; a hollow sheet having one or more hollow portions; and a second substrate which transmits the first light, wherein the first substrate, the hollow sheet, and the second substrate are attached to each other, with the hollow sheet being positioned between the first substrate, which underlies the hollow sheet, and the second substrate which overlies the hollow sheet, wherein the one or more hollow portions of the hollow sheet are enclosed by the optical filter of the underlying first substrate, the hollow sheet, and the overlying second substrate and form one or more flow passages; one or more inlet and outlet holes on one of the first substrate and the second substrate and in fluid communication with the one or more flow passages; a plurality of bead carriers, a surface of each of which bead carriers carries a plurality of molecules of the nucleotide having the intramolecular fluorescent molecule via the photocleavable linker, fixed inside the one or more flow passages, and wherein the optical filter transmits a second light for exciting the fluorescent molecule and transmits a third light emitted from the fluorescent molecule. 2. The flow cell for nucleic acid analysis according to claim 1 , wherein the optical filter is patterned such that the optical filter is in contact with the one or more flow passages. 3. The flow cell for nucleic acid analysis according to claim 1 , wherein the second substrate comprises a near-ultraviolet ray cut filter transmitting the first light while reflecting a fourth light having a wavelength shorter than that of the first light. 4. The flow cell for nucleic acid analysis according to claim 1 , wherein the second substrate comprises an antireflection film preventing reflection of the first light and the second light. 5. The flow cell for nucleic acid analysis according to claim 1 , wherein a wavelength of the first light is 450 nm or less. 6. The flow cell for nucleic acid analysis according to claim 1 , wherein a wavelength of the first light is 320 nm or more. 7. The flow cell for nucleic acid analysis according to claim 1 , wherein a wavelength of the second light is 450 nm or more. 8. The flow cell for nucleic acid analysis according to claim 1 , wherein a wavelength of the third light is 480 nm or more. 9. A flow cell for nucleic acid analysis, comprising: a first substrate and a second substrate attached to each other, a plurality of hollow passage grooves in the first substrate and forming flow passages, and an optical filter on the first substrate, which optical filter reflects a first light for carrying out a photo-cleaving reaction with a nucleotide having an intramolecular fluorescent molecule via a photocleavable linker, on a bottom surface of the flow passages formed by the passage grooves, and the second substrate transmits the first light; a plurality of bead carriers, a surface of which carries a plurality of molecules of the nucleotide having the intramolecular fluorescent molecule via the photocleavable linker, fixed inside the flow passages formed by the passage grooves, wherein the optical filter transmits a second light for exciting the fluorescent molecule and transmits a third light emitted from the fluorescent molecule, and wherein the passage grooves are enclosed by the optical filter of the attached first substrate and second substrate. 10. A flow cell for nucleic acid analysis, comprising: a first substrate and a second substrate attached to each other, a plurality of hollow passage grooves in the second substrate and forming flow passages, a surface of the first substrate opposite to the passage grooves being provided with an optical filter, which optical filter reflects a first light for carrying out a photo-cleaving reaction with a nucleotide having an intramolecular fluorescent molecule via a photocleavable linker, and the second substrate transmits the first light; a plurality of bead carriers, a surface of each of which bead carriers carries a plurality of molecules of the nucleotide having the intramolecular fluorescent molecule via the photocleavable linker, are fixed inside the flow passages formed by the passage grooves, wherein the optical filter transmits a second light for exciting the fluorescent molecule and transmits a third light emitted from the fluorescent molecule, and wherein the passage grooves are enclosed by the attached first substrate and the second substrate. 11. A flow cell for nucleic acid analysis, comprising: a first substrate and a second substrate attached to each other; a sheet disposed between the first and second substrates, a plurality of hollow passage grooves in the sheet and forming flow passages, a bottom surface of the passage grooves on a side of the first substrate being defined by an optical filter, which optical filter reflects a first light for carrying out a photo-cleaving reaction with a nucleotide having an intramolecular fluorescent molecule via a photocleavable linker, and wherein the second substrate transmits the first light; a plurality of bead carriers, a surface of each of which bead carriers carries a plurality of molecules of the nucleotide having the intramolecular fluorescent molecule via the photocleavable linker, fixed inside the flow passage, wherein the optical filter transmits a second light for exciting the fluorescent molecule and transmits a third light irradiated from the fluorescent molecule, and wherein the flow passages formed by passage grooves are enclosed by the attached first substrate and the second substrate. 12. A nucleic acid analyzer for analyzing nucleic acid, the analyzer comprising: a flow cell for nucleic acid analysis including: a first substrate provided with an optical filter which reflects a first light for carrying out a photo-cleaving reaction with a nucleotide having an intramolecular fluorescent molecule via a photocleavable linker; a hollow sheet having one or more hollow portions; a second substrate which transmits the first light, the first substrate, the hollow sheet, and the second substrate are attached to each other with the hollow sheet being positioned between the first substrate, which underlies the hollow sheet, and the second substrate, which overlies the hollow sheet, wherein the one or more hollow spaces, which are enclosed by the optical filter of the underlying first substrate, the hollow sheet, and the overlying second substrate form one or more flow passages, wherein the optical filter transmits a second light for exciting the fluorescent molecule and transmits a third light irradiated from a fluorescent molecule; a holder unit configured to hold the flow cell for nucleic acid analysis and including; a light source configured to irradiate the flow cell for nucleic acid analysis with the first light for changing a structure of the substance in the one or more flow passages; a detection unit configured to irradiate the flow cell with a second light, and observe the third light from the fluorescent molecule corresponding to a sample in the flow cell, and wherein a plurality of bead carriers, a surface of each of which bead carriers carries a plurality of molecules of the nucleotide having the intramolecular fluorescent molecule via the photocleavable linker, are fixed inside the one or more flow passages.
for parallel transport of multiple samples · CPC title
Methods for sequencing · CPC title
Cards, e.g. flat sample carriers usually with flow in two horizontal directions · CPC title
characterised by interfacing components, e.g. fluidic, electrical, optical or mechanical interfaces · CPC title
Flow chambers · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.