TY - JOUR
T1 - Semi-automated direct colorimetric measurement of creatine kinase isoenzyme MB activity after extraction from serum by use of a CK-MB-specific monoclonal antibody
AU - Landt, Y.
AU - Vaidya, H. C.
AU - Porter, S. E.
AU - Whalen, K.
AU - McClellan, A.
AU - Amyx, C.
AU - Parvin, C. A.
AU - Kessler, G.
AU - Nahm, M. H.
AU - Dietzler, D. N.
AU - Ladenson, J. H.
PY - 1988
Y1 - 1988
N2 - This semi-automated colorimetic assay for the MB isoenzyme of creatine kinase (EC 2.7.3.2) is based on a monoclonal antibody ('Conan-MB') specific for this isoenzyme and is a modification of a previously published method (Vaidya et al., Clin Chem 1986; 32: 657-63). A 0.64-cm bead coated with 2 to 3 μg of antibody is incubated with 100 μL of serum and 10 μL of 0.2 mol/L β-mercaptoethanol for 1 h at room temperature, to extract CK-MB. The beads are washed with de-ionized water and incubated with CK substrate for 45 min at 37°C. A solution containing trans-1,2-diaminocyclohexane-N, N, N', N'-tetraacetic acid, p-iodonitrotetrazolium violet, and diaphorase is added and the resulting colored product is measured at 492 nm. The standard curve is linear to 200 U of CK-MB per liter, and analytical recovery is 97-113%. Total assay CV for low (9.7 U/L) and high (50.7 U/L) quality-control materials was 14.1% (n = 1878) and 11.6% (n = 1842), respectively. CK-MB activity correlated well (r = 0.978, n = 226) with CK-MB measured by a two-site mass immunoassay, and 99.4% of samples with CK-MB ≥ 12 U/L (n = 347) were verified by electrophoresis on agarose.
AB - This semi-automated colorimetic assay for the MB isoenzyme of creatine kinase (EC 2.7.3.2) is based on a monoclonal antibody ('Conan-MB') specific for this isoenzyme and is a modification of a previously published method (Vaidya et al., Clin Chem 1986; 32: 657-63). A 0.64-cm bead coated with 2 to 3 μg of antibody is incubated with 100 μL of serum and 10 μL of 0.2 mol/L β-mercaptoethanol for 1 h at room temperature, to extract CK-MB. The beads are washed with de-ionized water and incubated with CK substrate for 45 min at 37°C. A solution containing trans-1,2-diaminocyclohexane-N, N, N', N'-tetraacetic acid, p-iodonitrotetrazolium violet, and diaphorase is added and the resulting colored product is measured at 492 nm. The standard curve is linear to 200 U of CK-MB per liter, and analytical recovery is 97-113%. Total assay CV for low (9.7 U/L) and high (50.7 U/L) quality-control materials was 14.1% (n = 1878) and 11.6% (n = 1842), respectively. CK-MB activity correlated well (r = 0.978, n = 226) with CK-MB measured by a two-site mass immunoassay, and 99.4% of samples with CK-MB ≥ 12 U/L (n = 347) were verified by electrophoresis on agarose.
UR - https://www.scopus.com/pages/publications/0023898519
U2 - 10.1093/clinchem/34.3.575
DO - 10.1093/clinchem/34.3.575
M3 - Article
C2 - 3349610
AN - SCOPUS:0023898519
SN - 0009-9147
VL - 34
SP - 575
EP - 581
JO - Clinical chemistry
JF - Clinical chemistry
IS - 3
ER -