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用RNase保护法定量检测鲤鱼组织IGF-ImRNA的表达 被引量:4

Quantitative Detection of Common Carp IGFI mRNA Expression by RNase Protection Assay
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摘要 建立了定量分析mRNA表达的RNase保护法,并用于鲤鱼IGF-I的研究.结果表明鲤鱼IGF-ImRNA在肝组织的丰度为每微克DNA含50.45×10-17mol,在其他组织有少量IGF-ImRNA表达. Insulinlike growth factorI interests many investigators because of its importance in mediating most growth effects of growth hormone. To study carp IGFI expression, we established the quantitative method for detecting mRNA, RNase Protection Assay (RPA). This technique is rapid and requires minimal sample manipulation, allowing the analysis of hundreds of samples simultaneously. From the study on common carp, the hepatic IGFI mRNA expression was shown highest, 5445×10-17 mol/μg DNA. In other tissues, low amount of IGFI mRNA was also expressed.
出处 《中山大学学报(自然科学版)》 CAS CSCD 北大核心 1998年第4期121-124,共4页 Acta Scientiarum Naturalium Universitatis Sunyatseni
基金 中山大学基础学科前沿课题基金
关键词 RNase保护法 IGF-ImRNA 鲤鱼 MRNA 表达 RNase Protection Assay, insulinlike growth factorI, hybridization,common carp
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参考文献2

  • 1Liang Y H,Mol Mar Biol Biotechnol,1996年,5卷,2期,145页
  • 2Chen T T,Molecular Endocrinology of Fish, Fish Physiology (Vol Ⅷ),1994年,179页

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