Methods and arrays for producing and sequencing monoclonal clusters of nucleic acid
US-10619204-B2 · Apr 14, 2020 · US
US11938475B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11938475-B2 |
| Application number | US-202017114134-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 7, 2020 |
| Priority date | Dec 21, 2017 |
| Publication date | Mar 26, 2024 |
| Grant date | Mar 26, 2024 |
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.
In an example of the method, a functionalized coating layer is applied in depressions of a patterned flow cell substrate. The depressions are separated by interstitial regions. A primer is grafted to the functionalized coating layer to form a grafted functionalized coating layer in the depressions. A hydrogel is applied on at least the grafted functionalized coating layer.
Opening claim text (preview).
What is claimed is: 1. A method, comprising: applying a functionalized coating layer in depressions of a patterned flow cell substrate, wherein the depressions are separated by interstitial regions and wherein the patterned flow cell substrate includes a bonding region; grafting a primer to the functionalized coating layer to form a grafted functionalized coating layer in the depressions; applying a non-grafted hydrogel on at least the grafted functionalized coating layer, the non-grafted hydrogel being selected from the group consisting of crosslinked polyacrylamide, an agarose gel, and crosslinked polyethylene glycol; and bonding a lid to the patterned flow cell substrate at the bonding region, thereby defining a flow channel between the patterned flow cell substrate and the lid. 2. The method as defined in claim 1 , wherein the non-grafted hydrogel is disposed on the grafted functionalized coating layer and on some of the interstitial regions. 3. The method as defined in claim 1 , wherein prior to applying the functionalized coating layer, the method further comprises treating a surface of the patterned flow cell substrate to attach a functional group to the surface to form treated depressions and treated interstitial regions. 4. The method as defined in claim 3 , wherein applying the functionalized coating layer in the depressions includes: applying the functionalized coating layer in the treated depressions and on the treated interstitial regions; and polishing the functionalized coating layer from the treated interstitial regions. 5. The method as defined in claim 1 , wherein applying the non-grafted hydrogel involves applying an aqueous mixture including from about 0.001% up to about 0.1% (mass to volume) of a hydrogel material. 6. The method as defined in claim 1 , wherein the bonding region of the patterned flow cell substrate has a spacer layer bonded thereto, and wherein after the non-grafted hydrogel is applied, the bonding of the lid to the patterned flow cell substrate comprises bonding the lid to the spacer layer. 7. The method as defined in claim 1 , wherein applying the non-grafted hydrogel includes selectively depositing the non-grafted hydrogel on the grafted functionalized coating layer.
Agar-agar; Derivatives thereof · CPC title
characterised by the manufacture of the container or its components · CPC title
fluorescence · CPC title
Cards, e.g. flat sample carriers usually with flow in two horizontal directions · CPC title
Peptide nucleic acids [PNA] · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.