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微量双缩脲法(BCA)测定。

Bicinchoninic acid (BCA) assay in low volume.

机构信息

Department of Pathology and the Life Sciences Institute, University of Michigan, Ann Arbor, MI 48109, USA.

出版信息

Anal Biochem. 2011 Mar 15;410(2):310-2. doi: 10.1016/j.ab.2010.11.015. Epub 2010 Nov 13.

Abstract

The BCA assay is a colorimetric method for estimating protein concentration. In 96-well plates, the relationship between protein content and absorbance is nearly linear over a wide range; however, performance is reduced in lower volume. To overcome this limitation, we performed the BCA assays in opaque, white 384-well plates. These plates emit fluorescence between 450-600 nm when excited at 430 nm; thus, their fluorescence is quenched by the BCA chromophore (λ(max) 562 nm). This arrangement allowed accurate determination of protein content using only 2 μL of sample. Moreover, soluble flourescein could replace the white plates, creating a homogenous format.

摘要

BCA 法是一种用于估计蛋白质浓度的比色法。在 96 孔板中,蛋白质含量与吸光度之间的关系在很宽的范围内几乎呈线性;然而,在较低体积下性能会降低。为了克服这一限制,我们在不透明的白色 384 孔板中进行 BCA 分析。这些板在 430nm 激发时在 450-600nm 之间发出荧光;因此,它们的荧光被 BCA 生色团(λ(max)562nm)猝灭。这种设计仅使用 2μL 的样品即可准确测定蛋白质含量。此外,可溶性荧光素可以替代白色板,形成均匀的格式。

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