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首页> 外文期刊>Journal of Chinese Pharmaceutical Sciences >Application of L-Cys-Capped CdS Nanoparticles in Determination of Nucleic Acid by Resonance Light-Scattering Technique
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Application of L-Cys-Capped CdS Nanoparticles in Determination of Nucleic Acid by Resonance Light-Scattering Technique

机译:L-Cys包覆的CdS纳米颗粒在共振光散射技术测定核酸中的应用

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摘要

Aim To determine nucleic acid (DNA) using Nanometer-sized L-cysteine-capped CdS particles by resonance light scattering (RLS) method. Methods The nano-particles synthesized by a colloidal aqueous method were water-soluble, stable, and highly luminescent. The RLS of L-Cys-CdS particles were greatly quenched by DNA in Tris-HCl solutions. The intensity of RLS at 344 nm was proportional to the concentration of DNA. Results The linearity range of the calibration curve was 0.01 -1.0 μg·mL~(-1) for calf thymus DNA and 0.04 - 1.5 μg·mL~(-1) for salmon sperm DNA. The detection limits (3 δ) were 8 ng·mL~(-1) for calf thymus DNA and 10 ng·mL~(-1) for salmon sperm DNA. Conclusion This method is simple, sensitive, and capable of avoiding the use of toxic dyes.
机译:目的通过共振光散射(RLS)方法,使用纳米级L-半胱氨酸加帽的CdS颗粒测定核酸(DNA)。方法通过胶体水法合成的纳米粒子具有水溶性,稳定性和高发光性。 L-Cys-CdS颗粒的RLS在Tris-HCl溶液中被DNA极大地淬灭。 344 nm处的RLS强度与DNA浓度成正比。结果小牛胸腺DNA的校准曲线线性范围为0.01 -1.0μg·mL〜(-1),鲑鱼精子DNA的校准曲线线性范围为0.04-1.5μg·mL〜(-1)。小牛胸腺DNA的检出限(3δ)为8 ng·mL〜(-1),鲑鱼精子DNA的检出限为10 ng·mL〜(-1)。结论该方法简便,灵敏,可避免使用有毒染料。

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