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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 >Interaction of morin-cetyltrimethylammonium bromide with nucleic acids and determination of nucleic acids at nanograms per milliliter levels based on the enhancement of preresonance light scattering
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Interaction of morin-cetyltrimethylammonium bromide with nucleic acids and determination of nucleic acids at nanograms per milliliter levels based on the enhancement of preresonance light scattering

机译:摩尔蛋白-鲸蜡基三甲基溴化铵与核酸的相互作用以及基于共振前光散射增强的纳克/毫升水平的核酸测定

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摘要

A new preresonance light scattering (PRLS) assay of nucleic acids is presented. At pH 7.30, the weak PRLS of morin-cetyltrimethylammonium bromide (CTMAB) can be greatly enhanced by the addition of nucleic acids, owing to the interaction between the nucleic acid and morin-CTMAB. After the addition of morin and CTMAB to DNA, the zeta potential of DNA decreases and changes from negative to positive, which is due to the formation of an associate, the aggregation of morin on nucleic acids and the electric neutralization between DNA and the cationic surfactant CTMAB. Mechanism studies showed that the enhanced PRLS comes from the aggregation of morin inthe presence of nucleic acids and CTMAB. The enhanced intensity of PRLS is in proportion to the concentration of nucleic acids in the range 7.5 x 10~(-9)-1.0 x 10~(-5) g ml~(-1) for calf thymus DNA, 7.5 x 10~(-9)-1.0 x 10~(-6) g ml~(-1) for salmon sperm DNA and 1.0 x 10~(-8)-1.0 x 10~(-6)g ml~(-1) for yeast RNA. The detection limits are 3.4, 6.2 and 4.1 ng ml~(-1) for calf thymus DNA, salmon sperm DNA and yeast RNA, respectively. Synthetic samples were analyzed satisfactorily.
机译:提出了一种新的核酸共振光散射(PRLS)测定法。在pH 7.30时,由于核酸和morin-CTMAB之间的相互作用,可以通过添加核酸极大地增强morin-乙酰基三甲基溴化铵(CTMAB)的弱PRLS。在向DNA中添加了morin和CTMAB之后,DNA的zeta电位会降低并从负变为正,这是由于缔合体的形成,morin在核酸上的聚集以及DNA与阳离子表面活性剂之间的电中和CTMAB。机理研究表明,增强的PRLS来源于存在核酸和CTMAB的茉莉花蛋白的聚集。 PRLS的增强强度与小牛胸腺DNA的7.5 x 10〜(-9)-1.0 x 10〜(-5)g ml〜(-1)范围内的核酸浓度成比例,为7.5 x 10〜鲑鱼精子DNA为(-9)-1.0 x 10〜(-6)g ml〜(-1),鲑鱼精子DNA为1.0 x 10〜(-8)-1.0 x 10〜(-6)g ml〜(-1)酵母RNA。小牛胸腺DNA,鲑鱼精子DNA和酵母RNA的检出限分别为3.4、6.2和4.1 ng ml〜(-1)。对合成样品进行了满意的分析。

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