Ding Li, Williams Kathi, Ausserer Walter, Bousse Luc, Dubrow Robert
Caliper Technologies Corp., 605 Fairchild Drive, Mountain View, CA 94043-2234, USA.
Anal Biochem. 2003 May 1;316(1):92-102. doi: 10.1016/s0003-2697(03)00037-x.
We have developed a LabChip-based plasmid assay that runs on the Agilent 2100 Bioanalyzer. The assay determines the sizes and relative concentrations of the multiple forms of plasmid samples. Twelve samples can be analyzed on each chip in an automated run lasting approximately 30min. By using a supercoiled DNA sizing standard of 2-16kb, the size of the analyzed plasmid can be determined. The resulting MW has a relative standard deviation (CV) <5% and error <5%. Plasmids from 2-8kb can be separated with resolution better than 1kb. Topological isoforms in a plasmid sample can also be separated. However, due to differential staining, the heterogeneity of plasmid samples can only be measured if the signal of each isomer peak can be calibrated with pure standards for every isomer form. For a typical plasmid preparation which predominately is in the supercoiled form, the normalized corrected peak area for the supercoiled form correlates with the plasmid concentration in a broad range of 1-100ng/microl. The measurement is semiquantitative with a CV lower than 20%. A number of applications of this assay on a Labchip will be shown.
我们开发了一种基于LabChip的质粒分析方法,该方法可在安捷伦2100生物分析仪上运行。该分析方法可确定质粒样品多种形式的大小和相对浓度。在每次持续约30分钟的自动运行中,每个芯片可分析12个样品。通过使用2-16kb的超螺旋DNA大小标准品,可确定所分析质粒的大小。所得的分子量具有相对标准偏差(CV)<5%且误差<5%。2-8kb的质粒可实现分辨率优于1kb的分离。质粒样品中的拓扑异构体也可被分离。然而,由于染色差异,只有当每个异构体峰的信号能用每种异构体形式的纯标准品进行校准时,才能测量质粒样品的异质性。对于主要为超螺旋形式的典型质粒制备物,超螺旋形式的标准化校正峰面积在1-100ng/微升的宽范围内与质粒浓度相关。该测量为半定量,CV低于20%。将展示该分析方法在Labchip上的一些应用。