METHOD FOR ASSAYING CREATINE KINASE MB ISOZYME AND KIT TO BE USED THEREIN
The invention provides a method for measuring CK-MB in a sample by reacting the sample with a first antibody against CK-MB, a second antibody against CK-MB which recognizes an epitope different from that recognized by the first antibody, and an anti-CK-B antibody which recognizes a region of the 1st to 100th amino acid from N-terminus of the amino acid sequence of the subunit B of creatine kinase (step 1); measuring an optical change generated by the reaction (step 2); and determining a quantity of CK-MB in the sample on the basis of the result obtained in the step 2 (step 3). The invention also provides a kit to be used in the method, and a method for avoiding influence of creatine kinase BB isozyme in measuring CK-MB, comprising treating a sample with the anti-CK-B antibody.
1 . A method for measuring creatine kinase MB isozyme (CK-MB) in a sample, comprising:
(1) a step for reacting the sample with an anti-CK-B antibody which recognizes a region of the 1st to 100th amino acids from N-terminus in the amino acid sequence of a subunit B of creatine kinase, and then reacting with a first antibody against CK-MB a second antibody against CK-MB which recognizes an epitope different from that recognized by the first antibody, (step 1);
(2) a step for measuring an optical change generated by the reaction (step 2); and
(3) a step for determining a quantity of CK-MB in the sample on the basis of the result obtained in the step 2 (step 3).
2 . (canceled)
3 . The method according to claim 1 , wherein the region to be recognized by the anti-CK-B antibody is the one having an amino acid sequence shown in SEQ ID NO: 1.
4 . The method according to claim 1 , wherein the optical change is absorbance change, turbidity change, or scattered light intensity change.
5 . The method according to claim 1 , wherein the first antibody and/or the second antibody are immobilized on a insoluble carrier.
6 . The method according to claim 5 , wherein the insoluble carrier is latex particle.
7 . A method for avoiding a influence of creatine kinase BB isozyme (CK-BB) in measuring CK-MB, comprising treating a sample with an anti-CK-B antibody which recognizes a region of the 1st to 100th amino acid from N-terminus in the amino acid sequence of the subunit B of creatine kinase.
8 . A kit for measuring CK-MB comprising a first antibody against CK-MB, a second antibody against CK-MB which recognizes an epitope different from that recognized by the first antibody, and an anti-CK-B antibody which recognizes a region of the 1st to 100th amino acid from N-terminus in the amino acid sequence of the subunit B of creatine kinase.
9 . The kit according to claim 8 , comprising a first reagent containing the anti-CK-B antibody, and a second reagent containing the first antibody and the second antibody.
10 . The kit according to claim 8 , wherein the region recognized by the anti-CK-B antibody is the one having an amino acid sequence shown in SEQ ID NO: 1.
11 . The kit according to claim 8 , wherein the first antibody and/or the second antibody are immobilized on an insoluble carrier.
12 . The kit according to claim 11 , wherein the insoluble carrier is a latex particle.
13 . The method according to claim 1 , wherein the first antibody and the second antibody recognize both a subunit M and the subunit B of CK-MB.
14 . The method according to claim 1 , wherein the first antibody or the second antibody binds to the CK-MB and a CK-BB.
15 . The method according to claim 7 , wherein the CK-MB measurement is carried out using a first antibody against CK-MB and a second antibody against CK-MB which recognizes an epitope different from that recognized by the first antibody, and the measurement is influenced by CK-BB.
16 . The kit according to claim 8 , wherein the first antibody and the second antibody recognize both the subunit M and the subunit B of CK-MB.
17 . The kit according to claim 8 , wherein the first antibody or the second antibody binds to CK-MB and CK-BB.