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Large-scale expression screening by automated whole-mount in situ hybridization

机译:通过自动化全量原位杂交进行大规模表达筛选

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摘要

Gene expression profiling is an important component of functional genomics. We present a time and cost efficient high-throughput whole-mount in situ technique to perform a large-scale gene expression analysis in medaka fish (Oryzias latipes) embryos. Medaka is a model system ideally suited for the study of molecular genetics of vertebrate development. Random cDNA clones from an arrayed stage 20 medaka plasmid library were analyzed by whole-mount in situ hybridization on embryos of three representative stages of medaka development. cDNA inserts were colony PCR amplified in a 384-format. The PCR products were used to generate over 2000 antisense RNA digoxigenin probes in a high-throughput process. Whole-mount in situ hybridization was carried out in a robot and a broad range of expression patterns was observed. Partial cDNA sequences and expression patterns were documented with BLAST results, cluster analysis, images and descriptions, respectively; collectively this information was entered into a web-based database, 'MEPD' (http://www.embl-heidelberg.de/mepd/), that is publicly accessible.
机译:基因表达谱分析是功能基因组学的重要组成部分。我们提出了一种时间和成本有效的高通量全量原位技术,以在鱼(Oryzias latipes)胚胎中进行大规模的基因表达分析。 Medaka是一个模型系统,非常适合研究脊椎动物发育的分子遗传学。通过在medaka发育的三个代表性阶段的胚胎上进行全壁式原位杂交,分析了来自20阵列medaka质粒文库的随机cDNA克隆。 cDNA插入物以384格式集落PCR扩增。在高通量过程中,PCR产物用于产生2000多个反义RNA洋地黄毒苷探针。在机器人中进行了整装原位杂交,并观察到了广泛的表达模式。用BLAST结果,聚类分析,图像和描述分别记录了部分cDNA序列和表达模式。这些信息共同输入到基于Web的数据库“ MEPD”(http://www.embl-heidelberg.de/mepd/)中,该数据库可公开访问。

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