Hemolytic complement activity assay in microtitration plates.

Journal of applied biochemistry Pub Date : 1985-06-01
V R Muzykantov, G P Samokhin, M D Smirnov, S P Domogatsky
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Abstract

A new rapid technique is developed for the determination of complement activity in a large number of samples. Following serial dilution of complement, hemolysis is performed in the same microtiter plate. After the reaction, the degree of hemolysis in wells of the plate is determined spectrophotometrically by measurement of "absorbance" (light scattering) at 630 nm, without additional procedures. This method can find application in clinical and experimental biochemistry for the analysis of a large (up to thousands) number of samples.

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微量滴定板溶血补体活性测定。
建立了一种快速测定大量样品中补体活性的新方法。补体连续稀释后,溶血在同一微滴板上进行。反应后,通过测量630 nm的“吸光度”(光散射)分光光度法测定板孔中的溶血程度,不需要额外的程序。该方法可应用于临床和实验生物化学,用于分析大量(多达数千)样品。
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