Semi-automated direct colorimetric measurement of creatine kinase isoenzyme MB activity after extraction from serum by use of a CK-MB-specific monoclonal antibody

  • Y. Landt
  • , H. C. Vaidya
  • , S. E. Porter
  • , K. Whalen
  • , A. McClellan
  • , C. Amyx
  • , C. A. Parvin
  • , G. Kessler
  • , M. H. Nahm
  • , D. N. Dietzler
  • , J. H. Ladenson

Research output: Contribution to journalArticlepeer-review

13 Scopus citations

Abstract

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.

Original languageEnglish
Pages (from-to)575-581
Number of pages7
JournalClinical chemistry
Volume34
Issue number3
DOIs
StatePublished - 1988

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