WORKING WITH THE CONFOCAL SCANNING UV-LASER MICROSCOPE - SPECIFIC DNA LOCALIZATION AT HIGH-SENSITIVITY AND MULTIPLE-PARAMETER FLUORESCENCE

被引:21
作者
MONTAG, M
KUKULIES, J
JORGENS, R
GUNDLACH, H
TRENDELENBURG, MF
SPRING, H
机构
[1] GERMAN CANC RES CTR, INST EXPTL PATHOL, GENE STRUCT UNIT, W-6900 HEIDELBERG 1, GERMANY
[2] CARL ZEISS CO, DIV APPL MICROSCOPY, W-7082 OBERKOCHEN, GERMANY
关键词
CONFOCAL SCANNING LASER MICROSCOPY; UV-EXCITATION; MULTIPLE-PARAMETER FLUORESCENCE; IMMUNOFLUORESCENCE; LAMPBRUSH CHROMOSOME LOOPS; AMPHIBIAN OOCYTES; CHROMATIN ORGANIZATION; BLASTOCYST OUTGROWTHS; MAMMALIAN CELLS;
D O I
10.1111/j.1365-2818.1991.tb03172.x
中图分类号
TH742 [显微镜];
学科分类号
摘要
The use of fast-staining DNA-specific dyes such as DAPI or Hoechst 33342/33258 has been a major problem for confocal scanning laser microscopy (CSLM) studies of intranuclear chromatin organization. Moreover, the availability of a confocal ultra-violet scanning laser microscope configuration, which allows an excitation at wave-lengths of 364 nm as well as 488, 514 and 543 nm, is a prerequisite for single as well as multiple fluorescence parameter studies, especially if these studies are concerned with the precise localization of intranuclear signals. Here we report the characteristics and application of a CSLM, which was adapted for UV-excitation and therefore enables comparison of the spatial distribution of several types of signals within one preparation. In addition to multiple-parameter studies, we have also investigated the sensitivity of the system with regard to the identification of the double-stranded DNA of lampbrush chromosome loops in germinal vesicles of amphibian oocytes.
引用
收藏
页码:201 / 210
页数:10
相关论文
共 37 条
[1]  
AGARD DA, 1989, METHOD CELL BIOL, V30, P353
[2]  
AGARD DA, 1984, ANNU REV BIOPHYS BIO, V13, P191
[3]  
APPELS R, 1989, J CELL SCI, V92, P325
[4]   PROBING DNA-STRUCTURE AND FUNCTION WITH A MULTI-WAVELENGTH FLUORESCENCE CONFOCAL LASER MICROSCOPE [J].
ARNDTJOVIN, DJ ;
ROBERTNICOUD, M ;
JOVIN, TM .
JOURNAL OF MICROSCOPY, 1990, 157 :61-72
[5]   FLUORESCENCE DIGITAL IMAGING MICROSCOPY IN CELL BIOLOGY [J].
ARNDTJOVIN, DJ ;
ROBERTNICOUD, M ;
KAUFMAN, SJ ;
JOVIN, TM .
SCIENCE, 1985, 230 (4723) :247-256
[7]   COMBINING CONFOCAL AND CONVENTIONAL MODES IN TANDEM SCANNING REFLECTED LIGHT-MICROSCOPY [J].
BOYDE, A .
SCANNING, 1989, 11 (03) :147-152
[8]   3-DIMENSIONAL CHROMATIN DISTRIBUTION IN NEURO-BLASTOMA NUCLEI SHOWN BY CONFOCAL SCANNING LASER MICROSCOPY [J].
BRAKENHOFF, GJ ;
VANDERVOORT, HTM ;
VANSPRONSEN, EA ;
LINNEMANS, WAM ;
NANNINGA, N .
NATURE, 1985, 317 (6039) :748-749
[9]   2-PHOTON LASER SCANNING FLUORESCENCE MICROSCOPY [J].
DENK, W ;
STRICKLER, JH ;
WEBB, WW .
SCIENCE, 1990, 248 (4951) :73-76
[10]   IMAGING OF VIROIDS IN NUCLEI FROM TOMATO LEAF TISSUE BY INSITU HYBRIDIZATION AND CONFOCAL LASER SCANNING MICROSCOPY [J].
HARDERS, J ;
LUKACS, N ;
ROBERTNICOUD, M ;
JOVIN, TM ;
RIESNER, D .
EMBO JOURNAL, 1989, 8 (13) :3941-3949