Subtraction hybridization cDNA libraries from colon carcinoma and hepatic cancer

Clifford W. Schweinfest , Kelly W. Henderson , Jian-Ren Gu , Stavros D. Kottaridis , Stavros Besbeas , Evi Panotopoulou , Takis S. Papas
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引用次数: 71

Abstract

cDNA clones of differentially expressed mRNAs in a colon carcinoma and a hepatocellular carcinoma have been isolated by subtractive cDNA cloning. The subtracted material is at least 90 × enriched for differentially expressed sequences and can be used for construction of subtractive cDNA libraries and polymerase chain reaction (PCR) amplification to generate differential probes. Commercially available λZAP II is used for construction of primary libraries since single-stranded phage bearing the cloned cDNA can be excised in vivo and because λ libraries are convenient for subsequent screening and manipulations. Rare mRNAs (less than 0.01% abundance), which are differentially expressed, can be isolated utilizing this procedure.

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结肠癌和肝癌cDNA文库的减法杂交
用减法cDNA克隆技术分离了结肠癌和肝癌中差异表达mrna的cDNA克隆。缺失的材料对差异表达序列至少富集90倍,可用于构建缺失cDNA文库和聚合酶链反应(PCR)扩增以产生差异探针。由于携带克隆cDNA的单链噬菌体可以在体内切除,并且λ文库便于后续的筛选和操作,因此使用市售的λ zap II用于构建初级文库。利用这种方法可以分离出差异表达的罕见mrna(丰度小于0.01%)。
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Gene targeting in murine embryonic stem cells: Introduction of specific alterations into the mammalian genome A solution hybridization method for quantification of mRNAs: Determining the amount and stability of oncogene mRNA The use of transgenic mice for short-term, in vivo mutagenicity testing Author index volume 7 Subject index volume 7
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