An easy and reliable procedure of microdissection technique for the analysis of chromosomal breakpoints and marker chromosomes

被引:37
作者
Weimer, J
Kiechle, M
Senger, G
Wiedemann, U
Ovens-Raeder, A
Schuierer, S
Kautza, M
Siebert, R
Arnold, N
机构
[1] Univ Kiel, Frauenklin, D-24105 Kiel, Germany
[2] Praxis Dr S Ebner, D-93047 Regensburg, Germany
[3] Gemeinschaftspraxis Dr Med A Ovens Raeder C Walde, D-81545 Munich, Germany
[4] Kreiskrankenhaus Alt Neuotting, D-84503 Altotting, Germany
[5] Univ Kiel, Inst Human Genet, D-24105 Kiel, Germany
关键词
DOP-PCR; microdissection; reverse painting;
D O I
10.1023/A:1009263913478
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Microdissection in combination with reverse painting fluorescence in-situ hybridization (FISH) is a very effective method to identify breakpoints and rearrangements of derived chromosomes and reveal the chromosomal origin of marker chromosomes. We describe an innovation that allows a convenient, fast and safe isolation of microdissected fragments as currently available protocols. The microdissected chromosomes are harvested in a collection drop located in a movable micropipette adjusted to a second micromanipulator under microscopic observation. We used this technique to analyze several cytogenetic aberrations. In order to evaluate the efficiency of our microdissection procedure, we compared the results obtained with microdissection probes made from only one fragment with those obtained with more than six microdissected fragments. In all cases, the single- fragment microdissections were sufficient to provide probes.
引用
收藏
页码:355 / 362
页数:8
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