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首页> 外文期刊>The Analyst: The Analytical Journal of the Royal Society of Chemistry: A Monthly International Publication Dealing with All Branches of Analytical Chemistry >Image-based detection of oligonucleotides - a low cost alternative to spectrophotometric or fluorometric methods
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Image-based detection of oligonucleotides - a low cost alternative to spectrophotometric or fluorometric methods

机译:基于图像的寡核苷酸检测-分光光度法或荧光法的低成本替代品

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摘要

Herein, we report a sensitive and low cost image-based (photocolorimetric) method for the detection of oligonucleotides on an activated polypropylene microtest plate (APPμTP). The assay was developed on the APPμTP by covalently immobilising 20-mer amino-modified oligonucleotides. Biotin-tagged complementary target sequences were then hybridised with the immobilised oligonucleotides. Colour was developed by streptavidin-HRP conjugate and the image of the coloured assay solution was taken by a desktop scanner and analysed using colour saturation. The developed method was analysed for its detection limit, accuracy, sensitivity and interference. The linearity range was found to be 1.7- 170 ng mL~(-1) while the lower limit of detection and limit of quantification were 1.7 and 5.6 ng mL~(-1) respectively. The method showed comparable sensitivity to fluorometric methods, and was found to be correlated to fluorescence (R~2 = 0.8081, ρ-value < 0.0001) and absorbance (R~2 = 0.9394, ρ-value < 0.0001)-based quantification. It discriminates mismatched base sequences from perfectly matched sequences efficiently. Validation of the method was carried out by detecting por A DNA of Neisseria meningitidis in bacterial meningitis samples. The por A-specific probe having a 6-carbon spacer at its 50- NH2 terminus was immobilised covalently to the APPmTP and hybridised with different samples of biotinylated single-stranded por A DNA.
机译:在本文中,我们报告了一种灵敏且低成本的基于图像的(光度比色法)方法,用于在活化的聚丙烯微量检测板(APPμTP)上检测寡核苷酸。通过共价固定20-mer氨基修饰的寡核苷酸,在APPμTP上开发了该检测方法。然后将生物素标记的互补靶序列与固定的寡核苷酸杂交。通过链霉亲和素-HRP结合物显色,然后通过台式扫描仪拍摄彩色化验溶液的图像,并使用颜色饱和度进行分析。分析了该开发方法的检测限,准确性,灵敏度和干扰。线性范围为1.7- 170 ng mL〜(-1),而检测下限和定量限分别为1.7和5.6 ng mL〜(-1)。该方法显示出与荧光法相当的灵敏度,并且被发现与基于荧光的定量(R〜2 = 0.8081,ρ值<0.0001)和吸光度(R〜2 = 0.9394,ρ值<0.0001)相关。它可以有效地从完全匹配的序列中区分出不匹配的碱基序列。通过检测细菌性脑膜炎样品中脑膜炎奈瑟氏菌的por A DNA进行方法验证。将在其50-NH2末端具有6个碳间隔基的por A特异性探针共价固定在APPmTP上,并与生物素化的单链por A DNA的不同样品杂交。

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