Forman D T
Ann Clin Lab Sci. 1977 Jul-Aug;7(4):329-34.
Antisera against purified human placental alkaline phosphatase (PAP) and crystallized creatine kinase (CK) isoenzyme from human skeletal muscle (MM) were raised in rabbits. The PAP antiserum was shown by radial immunodiffusion not to react with purified alkaline phosphatases from human liver and intestine, nor with the alkaline phosphatase in sera from patients with osteoblastic bone disease. CK antiserum also demonstrated no cross-reaction and was precipitated quantitatively by its homologous antisera. A "rocket" electroimmunoassay for PAP and CK is described. The method is simple, reproducible and uses small volumes of antiserum. The isoenzyme patterns were compared with those developed by several electrophoretic methods. These techniques share with other immunoassay the advantages of specificity for the antigen and enhance the quantitation of isoenzyme assays.
用纯化的人胎盘碱性磷酸酶(PAP)和人骨骼肌结晶肌酸激酶(CK)同工酶(MM)免疫家兔制备抗血清。通过放射免疫扩散法表明,PAP抗血清与人肝和肠的纯化碱性磷酸酶不发生反应,也不与成骨性骨病患者血清中的碱性磷酸酶发生反应。CK抗血清也未显示交叉反应,并且被其同源抗血清定量沉淀。本文描述了一种用于PAP和CK的“火箭”电免疫测定法。该方法简单、可重复,并且使用少量抗血清。将同工酶谱与几种电泳方法所显示的谱进行了比较。这些技术与其他免疫测定法一样,具有对抗原特异性的优点,并提高了同工酶测定的定量能力。