Gray J W, Peters D, Merrill J T, Martin R, Van Dilla M A
J Histochem Cytochem. 1979 Jan;27(1):441-4. doi: 10.1177/27.1.374608.
A flow cytometer has been constructed which measures total fluorescence and the distribution of fluorescence along isolated, stained mammalian chromosomes. In this device, chromosomes flow lengthwise at 4 m/sec through a 1-micrometer thick laser beam. The fluorescence from each chromosome is recorded at 10 nsec intervals; the sequence of recorded values represents the distribution of fluorescence along the chromosome and is stored in the memory of a waveform recorder. The total fluorescence of each chromosome is also measured and recorded. Preliminary studies show that doublets of 1.83 micrometers diameter microspheres flow with their long axes parallel to the direction of flow and that the two microspheres are resolved in the slit-scan profile. Ethidium bromide stained Muntjac and Chinese hamster chromosomes have also been slit-scanned. Centromeres were resolved in many of the Nos. 1 and 2 Chinese hamster chromosomes and the Nos. 1 and X + 3 Muntjac chromosomes.
已构建了一种流式细胞仪,它可测量总荧光以及沿分离的、染色的哺乳动物染色体的荧光分布。在该装置中,染色体以4米/秒的速度沿长度方向流过1微米厚的激光束。每隔10纳秒记录一次每条染色体的荧光;记录值序列代表沿染色体的荧光分布,并存储在波形记录仪的内存中。还测量并记录了每条染色体的总荧光。初步研究表明,直径为1.83微米的微球双联体以其长轴平行于流动方向流动,并且在狭缝扫描轮廓中两个微球得以分辨。用溴化乙锭染色的麂和中国仓鼠染色体也进行了狭缝扫描。在许多中国仓鼠1号和2号染色体以及麂1号和X + 3号染色体中分辨出了着丝粒。