Method for Measuring Fibroblast Growth Factor-23 and Reagent Therefor
US-2024402163-A1 · Dec 5, 2024 · US
US9851356B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9851356-B2 |
| Application number | US-201214239449-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 13, 2012 |
| Priority date | Sep 14, 2011 |
| Publication date | Dec 26, 2017 |
| Grant date | Dec 26, 2017 |
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Provided is an invention relating to a method for measuring an anti-WT1 antibody in a sample allowing measurement and evaluation of the anti-WT1 antibody with higher accuracy and to use of the method. The method for measuring an anti-WT1 antibody in a sample includes using a polypeptide having antigenicity to the anti-WT1 antibody selected from a polypeptide comprising the amino acid sequence of positions 294-449 in SEQ ID NO: 1, a partial polypeptide of the polypeptide, and a polypeptide including an amino acid sequence having deletion, substitution, or addition of one to several amino acids in the amino acid sequence constituting each of these polypeptides and/or a polypeptide having antigenicity to the anti-WT1 antibody selected from a polypeptide comprising the amino acid sequence of positions 181-324 in SEQ ID NO: 1, a partial polypeptide of the polypeptide, and a polypeptide including an amino acid sequence having deletion, substitution, or addition of one to several amino acids in the amino acid sequence constituting each of these polypeptides.
Opening claim text (preview).
The invention claimed is: 1. A method for detecting an anti-WT1 antibody in a sample, comprising: contacting a sample with a polypeptide having antigenicity to the anti-WT1 antibody, wherein the polypeptide consists of the amino acid sequence of positions 294-449 in SEQ ID NO: 1; and detecting a concentration of the anti-WT1 antibody in the sample. 2. The method according to claim 1 , wherein the detecting comprises immobilizing the polypeptide to a solid phase; and detecting a reaction product between the immobilized polypeptide and an anti-WT1 antibody present in the sample to measure a concentration of the anti-WT1 antibody. 3. The method according to claim 1 , wherein the detecting of the concentration of the anti-WT1 antibody comprises performing one of radioimmunoassay, enzyme immunoassay, fluoroimmunoassay, indirect fluorescence assay, luminescent immunoassay, physicochemical assay, and Western blotting. 4. The method according to claim 1 , wherein the detecting of the concentration of the anti-WT1 antibody comprises performing ELISA. 5. A method for detecting a WT1-associated disease, comprising: contacting a sample from a subject with a polypeptide having antigenicity to an anti-WT1 antibody, wherein the polypeptide consists of the amino acid sequence of positions 294-449 in SEQ ID NO: 1; and detecting the anti-WT1 antibody in the subject. 6. The method according to claim 5 , wherein the WT1-associated disease is leukemia. 7. A method for predicting a responder to or for therapeutic monitoring of WT1 vaccine therapy of cancer, comprising: contacting a sample from a subject with a polypeptide having antigenicity to an anti-WT1 antibody, wherein the polypeptide consists of the amino acid sequence of positions 294-449 in SEQ ID NO: 1; and detecting the anti-WT1 antibody in the subject. 8. The method according to claim 7 , wherein the cancer is brain tumor or colon cancer. 9. A method of detecting immune response ability of a subject in a WT1-associated disease, comprising: detecting an anti-WT1 antibody in a sample taken from a subject having a WT1-associated disease by the method according to claim 1 , wherein presence of the anti-WT1 antibody indicates the subject's ability to show immune response. 10. The method according to claim 9 , wherein the WT1-associated disease is leukemia.
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