Attri A K, Minton K W
Anal Biochem. 1986 Nov 15;159(1):88-95. doi: 10.1016/0003-2697(86)90311-8.
We present a technique for analytical buoyant density sedimentation of nucleic acids which is performed in a preparative ultracentrifuge, in contrast to an analytical ultracentrifuge. Following centrifugation in a preparative rotor, small cylindrical quartz tubes are optically scanned; upon completion of the scan the data are processed immediately by a microcomputer and the buoyant density of the nucleic acid is calculated. Experimental data are presented employing several different deoxyribonucleic acids banded in neutral and alkaline cesium sulfate. Results are independent of rotor speed, location of bands within the gradient, and loading density of the cesium sulfate solution. Derived buoyant density values agree within 0.5% of previously published values.
我们介绍了一种核酸分析性浮力密度沉降技术,该技术是在制备型超速离心机中进行的,与分析型超速离心机不同。在制备型转子中离心后,对小圆柱形石英管进行光学扫描;扫描完成后,数据立即由微型计算机处理,并计算核酸的浮力密度。给出了使用几种不同的脱氧核糖核酸在中性和碱性硫酸铯中形成条带的实验数据。结果与转子速度、梯度内条带的位置以及硫酸铯溶液的加载密度无关。得出的浮力密度值与先前公布的值相差在0.5%以内。