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用于早期髓系谱系RNA的分子杂交探针的分离

Isolation of molecular hybridisation probes for early myeloid lineage RNAs.

作者信息

Mills K I, Anderson V A, Birnie G D

机构信息

Beatson Institute for Cancer Research, Garscube Estate, Bearsden, Glasgow, United Kingdom.

出版信息

Ann N Y Acad Sci. 1987;511:308-17. doi: 10.1111/j.1749-6632.1987.tb36259.x.

Abstract

Recombinant plasmid cDNA libraries representing the polyadenylated RNAs in the myeloid cell lines KG1 and ML1 have been constructed. The screening protocol has identified several clones which contain sequences homologous to RNAs expressed at high abundance in one or more of the myeloid cell lines KG1, ML1 and HL60. The relative abundances of RNAs homologous to three recombinants, pML15, pKG21 and pKGA/F5 were measured by an RNA dot hybridisation method in total RNAs isolated from peripheral blood leukocytes from leukaemic patients and normal individuals. High levels of these RNAs were observed mainly in ANLL and acute phase CML samples. The data suggest that these probes have the potential to sub-divide the ANLLs and to extend a molecular classification of the myeloid leukaemias.

摘要

已构建了代表髓系细胞系KG1和ML1中多聚腺苷酸化RNA的重组质粒cDNA文库。筛选方案已鉴定出几个克隆,这些克隆包含与在髓系细胞系KG1、ML1和HL60中的一种或多种中高丰度表达的RNA同源的序列。通过RNA点杂交法测量了与三种重组体pML15、pKG21和pKGA/F5同源的RNA在从白血病患者和正常个体的外周血白细胞中分离的总RNA中的相对丰度。主要在急性非淋巴细胞白血病(ANLL)和慢性粒细胞白血病(CML)急性期样本中观察到这些RNA的高水平。数据表明,这些探针有可能对ANLL进行细分,并扩展髓系白血病的分子分类。

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