Use of stroma for the detection of blood-group antibodies by ELISA.

D J Giannitsis, D Flierl, G Schuler, B Häcker-Shahin
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Abstract

A micro enzyme-linked immunosorbent assay (ELISA), using lyophilized stroma as carrier of red blood cell antigens, which stay stable longer than usual, using intact erythrocytes, was developed for determination of blood-group antibodies in the AB0, Kell and Lewis-systems. Stroma being fixed on microtiter plates was incubated with antisera and peroxidase-conjugated anti-human globulin. The transformation of the substrate added was determined photometrically. A binding of antibodies to the stroma could be demonstrated up to an antibody dilution of 1:1024 for the ABO-system, of 1:512 for the Kell-system and of 1:64 for the Lewis-system. By standardization of this method the quantitative determination of antibodies becomes possible without being restricted by the limited stability of intact erythrocytes.

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利用间质法ELISA检测血型抗体。
微酶联免疫吸附试验(ELISA),使用冻干基质作为红细胞抗原的载体,红细胞抗原比通常保持稳定的时间更长,使用完整的红细胞,用于测定AB0, Kell和lewis系统中的血型抗体。将基质固定在微滴板上,用抗血清和过氧化物酶结合的抗人球蛋白孵育。加入的底物的转变用光度法测定。抗体与基质的结合可被证明抗体稀释倍数为:abo系统为1:1024,kell系统为1:512,lewis系统为1:64。通过该方法的标准化,抗体的定量测定成为可能,而不受完整红细胞有限稳定性的限制。
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