Systems and methods for mechanogenetic functional ultrasound imaging
US-12172037-B2 · Dec 24, 2024 · US
US10093977B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10093977-B2 |
| Application number | US-52970108-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 28, 2008 |
| Priority date | Mar 5, 2007 |
| Publication date | Oct 9, 2018 |
| Grant date | Oct 9, 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.
Disclosed are: a nucleotide sequence and an amino acid sequence for CDR3 region of T-cell receptor (TCR) gene of WT1-specific cytotoxic T-cell (CTL) for WT1 protein; a method for the detection or treatment of cancer using the nucleotide sequence or the amino acid sequence; and a chip, a primer set, a kit, an apparatus and the like for use in the detection of cancer, each of which comprises the nucleotide sequence or the amino acid sequence.
Opening claim text (preview).
The invention claimed is: 1. A synthesized cDNA, comprising: (1) a nucleotide sequence encoding the entire amino acid sequence of a complementarity determining region 3 (CDR3) of a vβ chain of a T-cell receptor (TCR) of a WT1-specific HLA-A*2402-positive cytotoxic T-cell (CTL), wherein the nucleotide sequence is selected from the group consisting of SEQ ID NOs: 1-200, or (2) the nucleotide sequence that is complementary to the full length of the nucleotide sequence of (1), wherein the cDNA further comprises a label attached to the cDNA, said label selected from fluorescent labels, radioactive labels, enzyme labels, and chromophore labels. 2. The cDNA according to claim 1 , wherein said cDNA consists of: (1) the nucleotide sequence selected from the group consisting of SEQ ID NOs: 1-200, or (2) the nucleotide sequence that is complementary to the full length of the nucleotide sequence of (1): and the label. 3. The cDNA according to claim 1 , wherein the CDR3 is identified by comparing with a human TCR gene database.
for cancer (immunoassay for cancer G01N33/575) · CPC title
Receptors; Cell surface antigens; Cell surface determinants {(tumour specific antigens C07K14/4748)} · CPC title
Pharmacogenomics, i.e. genetic variability in individual responses to drugs and drug metabolism · CPC title
for tissue or cell typing, e.g. human leukocyte antigen [HLA] probes · CPC title
T-cell receptor (TcR)-CD3 complex · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.