Assay method for relaxin
AssigneeBellylabs Oy
InventorsAnni ESKELI, Mika SARAMÄKI
Life of this patent
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Abstract
The present invention relates to pregnancy testing in animals such as dogs and cats. In particular, the present invention provides assay methods for relaxin, and a kit for pregnancy testing in an animal, anti-relaxin antibodies and functional fragments thereof which can be used in the assay, hybridoma cell lines producing the same, nucleic acids encoding the same, and methods for producing the anti-relaxin antibodies and functional fragments thereof.
Claims15
An assay method for relaxin, wherein the method comprises
- (a) binding relaxin with a capture antibody comprising
- a VL domain comprising a CDR1 region having an amino acid sequence set forth in SEQ ID NO:
- 10, a CDR2 region having an amino acid sequence set forth in SEQ ID NO:
- 11, and a CDR3 region having an amino acid sequence set forth in SEQ ID NO:
- 12, and a VH domain comprising a CDR1 region having an amino acid sequence set forth in SEQ ID NO:
- 7, a CDR2 region having an amino acid sequence set forth in SEQ ID NO:
- 8, and a CDR3 region having an amino acid sequence set forth in SEQ ID NO:
- 9;
- or a functional fragment thereof which has independently at least 80% sequence identity, or at least 85%, 90%, 95%, 96%, 97%, 98% or 99% sequence identity to any one of SEQ ID NO:
- 7-12, wherein the functional fragment is capable of binding relaxin, in particular canine or feline relaxin, preferably canine relaxin;
- and
- (b) binding relaxin with a first detection antibody comprising
- a VL domain comprising a CDR1 region having an amino acid sequence set forth in SEQ ID NO:
- 4, a CDR2 region having an amino acid sequence set forth in SEQ ID NO:
- 5, and a CDR3 region having an amino acid sequence set forth in SEQ ID NO:
- 6, and a VH domain comprising a CDR1 region having an amino acid sequence set forth in SEQ ID NO:
- 1, a CDR2 region having an amino acid sequence set forth in SEQ ID NO:
- 2, and a CDR3 region having an amino acid sequence set forth in SEQ ID NO:
- 3;
- or a functional fragment thereof which has independently at least 80% sequence identity, or at least 85%, 90%, 95%, 96%, 97%, 98% or 99% sequence identity to any one of SEQ ID NO:
- 1-6, wherein the functional fragment is capable of binding relaxin, in particular canine or feline relaxin, preferably canine relaxin;
- and
- (c) binding relaxin with a second detection antibody comprising
- a VL domain comprising a CDR1 region having an amino acid sequence set forth in SEQ ID NO:
- 16, a CDR2 region having an amino acid sequence set forth in SEQ ID NO:
- 17, and a CDR3 region having an amino acid sequence set forth in SEQ ID NO:
- 18, and a VH domain comprising a CDR1 region having an amino acid sequence set forth in SEQ ID NO:
- 13, a CDR2 region having an amino acid sequence set forth in SEQ ID NO:
- 14, and a CDR3 region having an amino acid sequence set forth in SEQ ID NO:
- 15;
- or a functional fragment thereof which has independently at least 80% sequence identity, or at least 85%, 90%, 95%, 96%, 97%, 98% or 99% sequence identity to any one of SEQ ID NO:
- 13-18, wherein the functional fragment is capable of binding relaxin, in particular canine or feline relaxin, preferably canine relaxin.
An assay method for relaxin, wherein the method comprises
- (a) binding relaxin with a capture antibody comprising
- a VH domain having an amino acid sequence set forth in SEQ ID NO:
- 21, and a VL domain having an amino acid sequence set forth in SEQ ID NO:
- 22;
- or a functional fragment thereof which has independently at least 80% sequence identity, or at least 85%, 90%, 95%, 96%, 97%, 98% or 99% sequence identity to any one of SEQ ID NO:
- 21 or 22, wherein the functional fragment is capable of binding relaxin, in particular canine or feline relaxin, preferably canine relaxin;
- and
- (b) binding relaxin with a first detection antibody comprising
- a VH domain having an amino acid sequence set forth in SEQ ID NO:
- 19, and a VL domain having an amino acid sequence set forth in SEQ ID NO:
- 20;
- or a functional fragment thereof which has independently at least 80% sequence identity, or at least 85%, 90%, 95%, 96%, 97%, 98% or 99% sequence identity to any one of SEQ ID NO:
- 19 or 20, wherein the functional fragment is capable of binding relaxin, in particular canine or feline relaxin, preferably canine relaxin;
- and
- (c) binding relaxin with a second detection antibody comprising
- a VH domain having an amino acid sequence set forth in SEQ ID NO:
- 23, and a VL domain having an amino acid sequence set forth in SEQ ID NO:
- 24;
- or a functional fragment thereof which has independently at least 80% sequence identity, or at least 85%, 90%, 95%, 96%, 97%, 98% or 99% sequence identity to any one of SEQ ID NO:
- 23 or 24, wherein the functional fragment is capable of binding relaxin, in particular canine or feline relaxin, preferably canine relaxin.
An anti-relaxin antibody or functional fragment thereof, wherein said antibody or functional fragment comprises
- (i) a VL domain comprising a CDR1 region having an amino acid sequence set forth in SEQ ID NO:
- 10, a CDR2 region having an amino acid sequence set forth in SEQ ID NO:
- 11, and a CDR3 region having an amino acid sequence set forth in SEQ ID NO:
- 12, and a VH domain comprising a CDR1 region having an amino acid sequence set forth in SEQ ID NO:
- 7, a CDR2 region having an amino acid sequence set forth in SEQ ID NO:
- 8, and a CDR3 region having an amino acid sequence set forth in SEQ ID NO:
- 9;
- or a functional fragment thereof which has independently at least 80% sequence identity, or at least 85%, 90%, 95%, 96%, 97%, 98% or 99% sequence identity to any one of SEQ ID NO:
- 7-12, wherein the functional fragment is capable of binding relaxin, in particular canine or feline relaxin, preferably canine relaxin;
- or
- (ii) a VL domain comprising a CDR1 region having an amino acid sequence set forth in SEQ ID NO:
- 4, a CDR2 region having an amino acid sequence set forth in SEQ ID NO:
- 5, and a CDR3 region having an amino acid sequence set forth in SEQ ID NO:
- 6, and a VH domain comprising a CDR1 region having an amino acid sequence set forth in SEQ ID NO:
- 1, a CDR2 region having an amino acid sequence set forth in SEQ ID NO:
- 2, and a CDR3 region having an amino acid sequence set forth in SEQ ID NO:
- 3;
- or a functional fragment thereof which has independently at least 80% sequence identity, or at least 85%, 90%, 95%, 96%, 97%, 98% or 99% sequence identity to any one of SEQ ID NO:
- 1-6, wherein the functional fragment is capable of binding relaxin, in particular canine or feline relaxin, preferably canine relaxin;
- or
- (iii) a VL domain comprising a CDR1 region having an amino acid sequence set forth in SEQ ID NO:
- 16, a CDR2 region having an amino acid sequence set forth in SEQ ID NO:
- 17, and a CDR3 region having an amino acid sequence set forth in SEQ ID NO:
- 18, and a VH domain comprising a CDR1 region having an amino acid sequence set forth in SEQ ID NO:
- 13, a CDR2 region having an amino acid sequence set forth in SEQ ID NO:
- 14, and a CDR3 region having an amino acid sequence set forth in SEQ ID NO:
- 15;
- or a functional fragment thereof which has independently at least 80% sequence identity, or at least 85%, 90%, 95%, 96%, 97%, 98% or 99% sequence identity to any one of SEQ ID NO:
- 13-18, wherein the functional fragment is capable of binding relaxin, in particular canine or feline relaxin, preferably canine relaxin.
An anti-relaxin antibody or functional fragment thereof, wherein said antibody or functional fragment comprises
- (i) a VH domain having an amino acid sequence set forth in SEQ ID NO:
- 19, and a VL domain having an amino acid sequence set forth in SEQ ID NO:
- 20, or
- (ii) a VH domain having an amino acid sequence set forth in SEQ ID NO:
- 21, and a VL domain having an amino acid sequence set forth in SEQ ID NO:
- 22, or
- (iii) a VH domain having an amino acid sequence set forth in SEQ ID NO:
- 23, and a VL domain having an amino acid sequence set forth in SEQ ID NO:
- 24;
- and wherein the functional fragment thereof has independently at least 80% sequence identity, or at least 85%, 90%, 95%, 96%, 97%, 98% or 99% sequence identity to any one of SEQ ID NO:
- 19, 20, 21, 22, 23, or 24, and wherein the functional fragment thereof is capable of binding relaxin, in particular canine or feline relaxin, preferably canine relaxin.
A cell line producing an anti-relaxin antibody, wherein the cell line is selected from
- (i) CCTCC C2021209,
- (ii) CCTCC C2021210, or
- (iii) CCTCC C2021211.
Dependencies are inferred from the claim text.