Schena M, Shalon D, Davis R W, Brown P O
Department of Biochemistry, Beckman Center, Stanford University Medical Center, CA 94305, USA.
Science. 1995 Oct 20;270(5235):467-70. doi: 10.1126/science.270.5235.467.
A high-capacity system was developed to monitor the expression of many genes in parallel. Microarrays prepared by high-speed robotic printing of complementary DNAs on glass were used for quantitative expression measurements of the corresponding genes. Because of the small format and high density of the arrays, hybridization volumes of 2 microliters could be used that enabled detection of rare transcripts in probe mixtures derived from 2 micrograms of total cellular messenger RNA. Differential expression measurements of 45 Arabidopsis genes were made by means of simultaneous, two-color fluorescence hybridization.
开发了一种高容量系统来并行监测许多基因的表达。通过在玻璃上高速机器人打印互补DNA制备的微阵列用于相应基因的定量表达测量。由于阵列的小尺寸和高密度,可以使用2微升的杂交体积,这使得能够检测来自2微克总细胞信使RNA的探针混合物中的稀有转录本。通过同时进行的双色荧光杂交对45个拟南芥基因进行差异表达测量。