首页> 外文期刊>Analytica chimica acta >Application of Western-blotting technique with chemiluminescence imaging to the study of haptoglobin type and haptoglobin complexes
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Application of Western-blotting technique with chemiluminescence imaging to the study of haptoglobin type and haptoglobin complexes

机译:化学发光成像的蛋白质印迹技术在触珠蛋白类型和触珠蛋白复合物研究中的应用

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摘要

Determination of haptoglobin (Hp) type and Hp complexes in human serum applying Western-blotting technique with enhanced chemiluminescence (ECL) imaging detection was developed in the present work. After separation of the proteins in serum by sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE), the target proteins were transferred to a nitrocellulose membrane. The membrane was incubated with a primary anti-human Hp followed by secondary horseradish peroxidase (HRP) conjugated IgG antibody. The ECL detection process was then carried out. Under the optimum conditions, the detection limits (3 times noise of baseline), calculated for Hp a(1), a(2) and beta subunits, respectively, are 1.25x10(-2) 7.5x10(-3), and 1.5x10(-4) g/l Five-fold repeated analysis of three serum samples with different Hp phenotypes show that the relative standard deviation (RSD) is ranging from 9.8% to 18.4% for within-blotting and between-blotting detection, respectively. A comparison was also carried out between ECL image and diaminobenzidine tetrahydrochloride (DAB) stain. A good correlation was obtained between the two methods (r=0.924), but the sensitivities of ECL imaging were improved by a factor of 20. The developed method was applied to the study of Hp binding to CD22, a B cell adhesion glycoprotein and Streptococcus pyogenes (S. pyogenes). The results showed that the Hp is bound to CD22 and to S. pyogenes, and the binding to S.pyogenes is Hp phenotype-dependent. (C) 1998 Elsevier Science B.V. [References: 16]
机译:在本工作中,开发了使用Western-blotting技术和增强的化学发光(ECL)成像检测技术测定人血清中的触珠蛋白(Hp)类型和Hp配合物的方法。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)分离血清中的蛋白质后,将目标蛋白质转移到硝酸纤维素膜上。膜与一级抗人Hp抗体,然后与辣根过氧化物酶(HRP)偶联的IgG抗体孵育。然后执行ECL检测过程。在最佳条件下,针对Hp a(1),a(2)和beta亚基计算出的检出限(基线噪声的3倍)分别为1.25x10(-2)7.5x10(-3)和1.5 x10(-4)g / l对三种具有不同Hp表型的血清样品进行五次重复分析,结果表明,对于印迹内检测和印迹间检测,相对标准偏差(RSD)分别为9.8%至18.4%。在ECL图像和二氨基联苯胺四盐酸盐(DAB)染色之间也进行了比较。两种方法之间具有良好的相关性(r = 0.924),但ECL成像的灵敏度提高了20倍。该发达的方法用于研究Hp与CD22,B细胞粘附糖蛋白和链球菌的结合。化脓(S. pyogenes)。结果表明,Hp与CD22和化脓链球菌结合,与化脓链球菌的结合是Hp表型依赖性的。 (C)1998 Elsevier Science B.V. [参考:16]

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