Wu Xia, Yang Jing He, Sun Shuna, Guo Changying, Ran Dehuan, Zheng Jinhua
Key Laboratory of Colloid and Interface Chemistry (Shandong University), Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, People's Republic of China.
Luminescence. 2006 May-Jun;21(3):129-34. doi: 10.1002/bio.896.
Nucleic acids can quench resonance light scattering (RLS) intensity of the Y(III)-1,6-bi(1'-phenyl-3'-methyl-5'-pyrazolone-4'-)hexane-dione(BPMPHD) complex in the pH range 5.0-5.8. Under optimal conditions, there are linear relationships between the quenching of RLS and the concentration of nucleic acids in the range 6.3 x 10(-8)-2.1 x 10(-5) g/mL for fish sperm DNA (fsDNA), 1.2 x 10(-8)-5.0 x 10(-5) g/mL for calf thymus DNA (ctDNA) and 6.0 x 10(-8)-2.0 x 10(-5) g/mL for yeast RNA (yRNA). The detection limits (3 s) of fsDNA, ctDNA and yRNA are 0.7 ng/mL, 3.8 ng/mL and 4.2 ng/mL, respectively.
在pH值为5.0 - 5.8的范围内,核酸能够猝灭Y(III)-1,6-双(1'-苯基-3'-甲基-5'-吡唑啉酮-4'-)己二酮(BPMPHD)配合物的共振光散射(RLS)强度。在最佳条件下,对于鱼精DNA(fsDNA),RLS猝灭与核酸浓度在6.3×10(-8)-2.1×10(-5) g/mL范围内呈线性关系;对于小牛胸腺DNA(ctDNA),在1.2×10(-8)-5.0×10(-5) g/mL范围内呈线性关系;对于酵母RNA(yRNA),在6.0×10(-8)-2.0×10(-5) g/mL范围内呈线性关系。fsDNA、ctDNA和yRNA的检测限(3s)分别为0.7 ng/mL、3.8 ng/mL和4.2 ng/mL。