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首页> 外文期刊>International Journal of Electrochemical Science >Electrochemical Detection of Single Nucleotide Polymorphism in Short DNA Sequences Related To Cattle Fatty Acid Binding Protein 4 Gene
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Electrochemical Detection of Single Nucleotide Polymorphism in Short DNA Sequences Related To Cattle Fatty Acid Binding Protein 4 Gene

机译:牛脂肪酸结合蛋白4基因短DNA序列中单核苷酸多态性的电化学检测。

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Electrochemical nucleic acid biosensor for detection of single nucleotide polymorphism (SNP) in Fattyacid binding protein 4 (FABP4) has been developed by immobilization of single stranded thiolatedprobe DNA (ss-DNA-SH) onto gold surfaces (ss-DNA-SH/Au) and its hybridization with wild andmutant complementary sequences related to Korean cattle FABP4 gene in the presence methyleneblue. The immobilization of ss-DNA-SH onto gold surfaces was characterized by atomic forcemicroscopy (AFM), Fourier transforms infrared microscopy (FT-IR), cyclic voltammetric (CV) andimpendence techniques. The SNP in Korean cattle FABP4 gene was detected by measuring themethylene blue accumulation on ss-DNA-SH/Au electrode hybridized with wild (wild-ds-DNA- SH/Au) and mutant (mutant-ds-DNA-SH/Au) complementary sequences using CV technique. The-1 sensitivities of wild-ds-DNA-SH/Au and mutant-ds-DNA-SH/Au electrodes are 0.0164 Ag L-1 with 0.998 regression coefficient (R) and 0.0122 Ag L with 0.993 R, respectively. The ssDNA- SH/Au electrode can detect the wild and mutant type complementary targets related to FABP4 gene in-1 the range of 5-10 ng L .
机译:通过将单链硫醇化探针DNA(ss-DNA-SH)固定在金表面(ss-DNA-SH / Au),已开发出用于检测脂肪酸结合蛋白4(FABP4)中单核苷酸多态性(SNP)的电化学核酸生物传感器。在亚甲基蓝存在下与韩国牛FABP4基因相关的野生突变互补序列杂交。通过原子力显微镜(AFM),傅立叶变换红外显微镜(FT-IR),循环伏安法(CV)和阻抗技术对ss-DNA-SH固定在金表面进行了表征。通过测量与野生(ds-DNA-SH / Au)和突变体(ds-DNA-SH / Au)突变的ss-DNA-SH / Au电极上的亚甲基蓝积累来检测韩国牛FABP4基因中的SNP使用CV技术的互补序列。野生型ds-DNA-SH / Au和突变型ds-DNA-SH / Au电极的-1灵敏度为0.0164 A / ng L-1(0.998回归系数)和0.0122 A / ng L(0.993 R),分别。 ssDNA-SH / Au电极可以在5-10 ng L的范围内检测与FABP4基因相关的野生型和突变型互补靶标。

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