Compositions and methods for accurately identifying mutations
US-2024409996-A1 · Dec 12, 2024 · US
US9803239B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9803239-B2 |
| Application number | US-201313840482-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 15, 2013 |
| Priority date | Mar 29, 2012 |
| Publication date | Oct 31, 2017 |
| Grant date | Oct 31, 2017 |
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Biochemical flow cells having sealed inlets and outlets are provided for performing high-volume assays on macromolecules. In one example embodiment, a flow cell with detachable inlet and outlet connectors comprises an inlet manifold, a coverslip, and a substrate disposed below the coverslip to form a reaction chamber, where the substrate is disposed to partially cover the inlet manifold such that a slit is formed along an entire edge of the substrate where fluids can flow from the inlet manifold through the slit, around substantially the entire edge of the substrate, and into the reaction chamber at equalized pressure and without bubbles. In another embodiment, a flow cell comprises an outlet manifold, two or more flow regions each connected to its own loading port via its own flow distribution funnel, each loading port connected to the outlet manifold, and plugs in a wall of the outlet manifold opposite each loading port, such that when a plug is absent from the wall of the outlet manifold, a loading tip may be inserted in its place, passing through the outlet manifold and connecting directly to a loading port.
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What is claimed is: 1. A flow cell comprising: a coverslip; a substrate spaced apart from the coverslip to form a reaction chamber between the coverslip and the substrate, the substrate comprising a first edge, a second edge opposed to the first edge, and an array of attachment sites on the substrate, wherein macromolecules introduced into the flow cell attach to the attachment sites; an outlet in fluid connection with the reaction chamber at or around the second edge of the substrate, the outlet comprising an outlet port; an inlet in fluid connection with the reaction chamber at or around the first edge of the substrate, the inlet comprising an inlet port and an inlet manifold, wherein the substrate partially covers the inlet manifold to define a space disposed in the inlet manifold below the substrate; and a bubble port in fluid communication with said space in the inlet manifold below the substrate, wherein the inlet manifold, the substrate, and the bubble port are configured such that bubbles trapped in said space are constrained to flow out of the bubble port without entering the reaction chamber, and whereby a fluid entering the flow cell by way of the inlet port and the inlet manifold is confined to flow around the first edge of the substrate and into the reaction chamber such that the fluid is substantially free of bubbles. 2. The flow cell of claim 1 further comprising a housing, wherein the inlet manifold is defined within the housing, and wherein an inlet slit is formed between the first edge of the substrate and a side of the housing that defines the inlet manifold. 3. The flow cell of claim 1 comprising inlet ports at opposite ends of the inlet manifold along an axis that is parallel to the first edge of the substrate. 4. The flow cell of claim 1 further comprising a housing that defines an outlet manifold, wherein an outlet slit is formed between the second edge of the substrate and a side of the housing that defines the outlet manifold, wherein fluid flowing out of the flow cell flows from the reaction chamber around the second edge of the substrate, through the outlet slit, into the outlet manifold and through the outlet port. 5. The flow cell of claim 1 further comprising a housing, wherein: the outlet comprises an outlet manifold comprising a wall that is configured to receive a plug or a loading tip for introducing a macromolecule into the flow cell; and the inlet manifold and the outlet manifold are defined within the housing. 6. The flow cell of claim 5 comprising outlet ports at opposite ends of the outlet manifold along an axis that is parallel to the second edge of the substrate. 7. The flow cell of claim 1 wherein the reaction chamber comprises two or more separate flow regions, each flow region comprising a loading port configured to receive a plug or a loading tip for introducing macromolecules into such flow region. 8. The flow cell of claim 1 wherein the inlet port is configured to receive an injector component comprising a make-and-break seal. 9. The flow cell of claim 8 wherein the inlet port is adapted to receive an injector component comprising a make-and-break seal having a shape selected from the group consisting of: a hemispherical shape with an annular cross-section, a conical shape, and a flat shape. 10. An apparatus configured for biological analysis of macromolecules comprising one or more flow cells of claim 1 . 11. The apparatus of claim 10 comprising a first station for performing a first operation on the flow cell, a second station for performing a second operation on the flow cell, and a transport device for moving the flow cell from the first station to the second station. 12. The apparatus of claim 10 for sequencing nucleic acids, wherein the macromolecules are nucleic acids. 13. A method of using the apparatus of claim 10 , the method comprising performing a first operation on the flow cell, transporting the flow cell to a second, different apparatus, and performing a second operation on the flow cell at the second apparatus. 14. The apparatus of claim 10 wherein the flow cell comprises one or more inlet ports that are configured to receive an injector component comprising a make-and-break seal. 15. The flow cell of claim 1 wherein the inlet slit has dimensions and/or a cross section that prevents bubbles from entering the reaction chamber.
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Cards, e.g. flat sample carriers usually with flow in two horizontal directions · CPC title
involving nucleic acid arrays, e.g. sequencing by hybridisation · CPC title
for microfluidic devices · CPC title
Seals · CPC title
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