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Western Blotting by Thin-Film Direct Coating

机译:薄膜直接镀膜进行蛋白质印迹

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A novel thin-film direct coating (TDC) technique was developed to markedly reduce the amount of antibody required for Western blotting (WB). Automatic application of the technique for a few seconds easily and homogeneously coats the specific primary antibody on the polyvinylidene fluoride (PVDF) membrane. While conventional WB requires 0.4 μg of the primary antibody, the proposed technique only uses 4 × 10~(-2) μg, which can be reduced further to 4 × 10~(-5) μg by reducing the coater width. Moreover, the proposed process reduces antibody probing times from 60 to 10 min. The quantification capability of TDC WB showed high linearity within a 4-log_2 dynamic range for detecting target antigen glutathione-S-transferase. Furthermore, TDC WB can specifically detect the extrinsic glutathione-S-transferase added in the Escherichia coli or 293T cell lysate with better staining sensitivity than conventional WB. TDC WB can also clearly probe the intrinsic β-actin, α-tubulin, and glyceraldehyde 3-phosphate dehydrogenase, which are usually used as control proteins in biological experiments. This novel technique has been shown to not only have valuable potential for increasing WB efficiency but also for providing significant material savings for future biomedical applications.
机译:开发了一种新颖的薄膜直接包被(TDC)技术来显着减少蛋白质印迹(WB)所需的抗体量。自动应用该技术只需几秒钟,即可轻松地将特定的一抗包被在聚偏二氟乙烯(PVDF)膜上。传统的WB需要0.4μg的一抗,而提出的技术仅使用4×10〜(-2)μg,可通过减小包被机宽度将其进一步减少至4×10〜(-5)μg。此外,提出的方法将抗体探测时间从60分钟减少到10分钟。 TDC WB的定量能力在4-log_2动态范围内显示出高线性,可检测目标抗原谷胱甘肽-S-转移酶。此外,TDC WB可以特异性检测添加到大肠杆菌或293T细胞裂解物中的外源性谷胱甘肽S-转移酶,具有比常规WB更好的染色敏感性。 TDC WB还可以清楚地探测固有的β-肌动蛋白,α-微管蛋白和3-磷酸甘油醛脱氢酶,它们通常在生物学实验中用作对照蛋白。这项新技术已被证明不仅具有提高WB效率的宝贵潜力,而且还为未来的生物医学应用节省了大量材料。

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