Clinical Chemistry · 1978 · 44 citations · 10 references
Life SciencesBiochemistryCellular MetabolismEnzymologyExercise PhysiologyEnzyme-linked Immunosorbent AssayMuscle Mass AssessmentAssayCreatine Kinase-mbEnzymesImmunoassay Cross-reactivityIsoenzyme SpecificityMuscle Enzyme TestingSerum BiomarkersSerum Creatine Kinase Assessment
Measurement of the mass concentration of serum enzymes by radioimmunoassay provides direct quantitation of specific isoenzymes and may be less subject to some of the limitations of traditional assay procedures for enzymes. We describe the development of a sensitive and specific radioimmunoassay for the muscle isoenzyme of creatine kinase, CM-MM, in human serum. CK-MM, purified from human skeletal muscle, was used to raise high-titer antisera and for iodination by the Chloramine T method. The radioimmunoassay required 50 microliter of sample, utilized a double-antibody separation method, and was completed in 24 h. Cross reactivity with CK-BB was virtually zero, 3--17% with CK-MB. The mass concentration of CK-MM in the serum of healthy subjects ranged from 36 to 1668 microgram/liter and correlated closely with total CK enzymatic activity. Serum concentrations of CK-MM from casually selected patients correlated less well with total CK enzymatic activity, suggesting the existence of other CK isoenzymes or the presence of inactive forms.
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Studies on adenosine triphosphate transphosphorylases
H.J. Keutel, Kazuhiro Okabe, Hans Jacobs et al. · Archives of Biochemistry and Biophysics · 1972 · 128 citations