Sensor, reagent, method for manufacturing probe molecule, and method for manufacturing polymer molecule
US-2019062818-A1 · Feb 28, 2019 · US
US12411133B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12411133-B2 |
| Application number | US-202117445486-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 19, 2021 |
| Priority date | Mar 19, 2021 |
| Publication date | Sep 9, 2025 |
| Grant date | Sep 9, 2025 |
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.
A chemical sensor device includes a sensor element; an oligopeptide mounted on a surface of the sensor element, the oligopeptide containing a first peptide sequence forming a β-sheet structure and a cysteine residue at a position different from the first peptide sequence; and a probe that is bonded to the cysteine residue and binds to or reacts with a specific substance.
Opening claim text (preview).
What is claimed is: 1. A chemical sensor device comprising: a sensor element having a surface; an oligopeptide mounted on the surface of the sensor element, the oligopeptide containing a first peptide sequence forming a β-sheet structure and a cysteine residue at a position different from the first peptide sequence; and a probe that is bonded to the cysteine residue and binds to or reacts with a specific substance, the cysteine residue being located at either a C-terminal or an N-terminal of the oligopeptide, and the probe being bonded to a sulfur atom of the cysteine residue via a succinimidyl group. 2. The device according to claim 1 , wherein the first peptide sequence consists of a repeating sequence of a glycine residue and an alanine residue. 3. The device according to claim 1 , wherein the first peptide sequence consists of a sequence containing a valine residue, an isoleucine residue, and a tyrosine residue. 4. The device according to claim 1 , wherein the probe is bonded to the oligopeptide via a sulfur atom of the cysteine residue. 5. The device according to claim 1 , wherein the probe is selected from a group consisting of a nucleic acid aptamer, a peptide aptamer, an enzyme, an antibody, a sugar chain, and a lectin. 6. The device according to claim 1 , wherein the sensor element is a charge detection element containing graphene. 7. A chemical sensor device comprising: a sensor element having a surface; an oligopeptide mounted on the surface of the sensor element, the oligopeptide containing a first peptide sequence forming a β-sheet structure and a cysteine residue at a position different from the first peptide sequence; and a probe that is bonded to the cysteine residue and binds to or reacts with a specific substance, the probe being bonded to a sulfur atom of the cysteine residue via a succinimidyl group.
involving physiochemical end-point determination, e.g. wave-guides, FETS, gratings · CPC title
Hybrid peptides {, i.e. peptides covalently bound to nucleic acids, or non-covalently bound protein-protein complexes} · CPC title
Carrier-bound or immobilised peptides (carrier-bound or immobilised enzymes C12N11/00); Preparation thereof · CPC title
specially adapted for biomolecules, e.g. gate electrode with immobilised receptors · CPC title
Electrodes · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.