Assays for IGFBP7 having improved performance in biological samples
The invention provides IGFBP7 immunoassays with improved clinical performance, particularly when used in the evaluation of renal injuries. The immunoassays rely on the selection and use of antibodies and antibody pairs that exhibit improved assay performance when used in complex clinical specimens such as biological fluids, and particularly when used in rapid assay formats such as lateral flow test devices.
1. An isolated antibody that binds to a human IGFBP7 protein, wherein the antibody comprises three complementarity determining regions of a light chain variable region having the amino acid sequence of SEQ ID NO: 9 and three complementarity determining regions of a heavy chain variable region having the amino acid sequence of SEQ ID NO: 10, wherein the complementarity determining regions are defined according to Kabat.
2. The antibody according to claim 1 , wherein the antibody is a monoclonal antibody.
3. The isolated antibody according to claim 1 , wherein the antibody is conjugated to a signal development element.
4. The isolated antibody according to claim 1 , wherein the antibody is conjugated to a solid support.
5. An immunoassay method for detecting the presence or amount of human IGFBP7, comprising:
contacting a sample with the antibody according to claim 1 ;
detecting binding of the human IGFBP7 in the sample to the antibody; and
relating the detected binding to the presence or amount of the human IGFBP7.
6. A nucleic acid encoding an antibody that binds to a human IGFBP7 protein, wherein the antibody comprises three complementarity determining regions of a light chain variable region having the amino acid sequence of SEQ ID NO: 9 and three complementarity determining regions of a heavy chain variable region having the amino acid sequence of SEQ ID NO: 10, wherein the complementarity determining regions are defined according to Kabat.
7. An antibody-expressing cell line, the cell line expressing an antibody that binds to a human IGFBP7 protein and comprises three complementarity determining regions of a light chain variable region having the amino acid sequence of SEQ ID NO: 9 and three complementarity determining regions of a heavy chain variable region having the amino acid sequence of SEQ ID NO: 10, wherein the complementarity determining regions are defined according to Kabat.
8. An isolated antibody that binds to a human IGFBP7protein, wherein the antibody comprises three complementarity determining regions of a light chain variable region having the amino acid sequence of SEQ ID NO: 11 and three complementarity determining regions of a heavy chain variable region having the amino acid sequence of SEQ ID NO: 12, wherein the complementarity determining regions are defined according to Kabat.
9. The antibody according to claim 8 , wherein the antibody is a monoclonal antibody.
10. The isolated antibody according to claim 8 , wherein the antibody is conjugated to a signal development element.
11. The isolated antibody according to claim 8 , wherein the antibody is conjugated to a solid support.
12. An immunoassay method for detecting the presence or amount of human IGFBP7, comprising:
contacting a sample with the antibody according to claim 8 ;
detecting binding of the human IGFBP7 in the sample to the antibody; and
relating the detected binding to the presence or amount of the human IGFBP7.
13. A nucleic acid encoding an antibody that binds to a human IGFBP7 protein, wherein the antibody comprises three complementarity determining regions of a light chain variable region having the amino acid sequence of SEQ ID NO: 11 and three complementarity determining regions of a heavy chain variable region having the amino acid sequence of SEQ ID NO: 12, wherein the complementarity determining regions are defined according to Kabat.
14. An antibody-expressing cell line, the cell line expressing an antibody that binds to a human IGFBP7 protein and comprises three complementarity determining regions of a light chain variable region having the amino acid sequence of SEQ ID NO: 11 and three complementarity determining regions of a heavy chain variable region having the amino acid sequence of SEQ ID NO: 12, wherein the complementarity determining regions are defined according to Kabat.