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脑脊液中蛋白质自动染料结合测定法的开发与评估

Development and evaluation of an automated dye-binding assay for protein in cerebrospinal fluid.

作者信息

Huang C M

机构信息

Clinical Pathology Department, Clinical Center, National Institutes of Health, Bethesda, MD 20892.

出版信息

Clin Chem. 1988 May;34(5):980-3.

PMID:3370801
Abstract

Addition of sodium dodecyl sulfate (SDS) to Coomassie Brilliant Blue reagent equalizes the binding variability of the dye to various proteins and markedly improves the accuracy of quantification of protein in cerebrospinal fluid. In the presence of SDS, the absorption spectrum and the absorption maximum are affected by reaction time and temperature, age of the dye preparation, and protein constituent. I automated this procedure, to optimize precision, enable use of a smaller sample, decrease hands-on time, maintain consistency in the time of reading, and avoid carryover. The results (y) compared well with those of the aca (x), with a Deming de-biased regression equation of y = 0.991x + 14.1 mg/L, Sy.x = 33.4 mg/L. The within-run and between-run precision (CV) was less than 2.5% and less than 4.5%, respectively. Commonly used antibiotics, flucytosine, or amphotericin B do not interfere. This automated procedure is fast and accurate and requires only 10 microL of sample.

摘要

在考马斯亮蓝试剂中添加十二烷基硫酸钠(SDS)可使染料与各种蛋白质的结合变异性均等化,并显著提高脑脊液中蛋白质定量的准确性。在SDS存在的情况下,吸收光谱和最大吸收值受反应时间、温度、染料制剂的保存时间以及蛋白质成分的影响。我将此程序自动化,以优化精密度、能够使用更少的样本、减少人工操作时间、保持读数时间的一致性并避免交叉污染。结果(y)与自动化学分析仪(aca)的结果(x)比较良好,Deming去偏回归方程为y = 0.991x + 14.1 mg/L,Sy.x = 33.4 mg/L。批内和批间精密度(CV)分别小于2.5%和小于4.5%。常用抗生素、氟胞嘧啶或两性霉素B无干扰。这种自动化程序快速准确,仅需10微升样本。

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