3.9 Article

A reporter system for reverse transfection cell arrays

期刊

JOURNAL OF BIOMOLECULAR SCREENING
卷 8, 期 6, 页码 620-623

出版社

SAGE PUBLICATIONS INC
DOI: 10.1177/1087057103259324

关键词

reverse transfection microarrays; surface-mediated transfection; serum response element (SRE) reporter construct; MAP kinase signaling proteins

资金

  1. NATIONAL CANCER INSTITUTE [R01CA017542, R37CA017542] Funding Source: NIH RePORTER
  2. NCI NIH HHS [CA17542] Funding Source: Medline

向作者/读者索取更多资源

The incredible speed of gene cloning and sequencing brought about by the genomic revolution has begun to outpace conventional gene discovery approaches in the pharmaceutical industry. High-throughput approaches for studying gene function in vivo are greatly needed. One potential answer to this challenge is reverse transfection, a high-throughput gene expression method for examining the function of hundreds to thousands of genes in parallel. One limitation of reverse transfection technology is the need for posttransfection processing of the arrays to analyze the activity of the expressed proteins. The authors have investigated the use of a reporter construct cotransfected with other genes of interest to monitor and screen gene function on reverse transfection microarrays. They developed a serum response element (SRE) reporter linked to the green fluorescent protein (GFP) that is cotransfected with target genes on reverse transfection arrays for monitoring mitogen-activated protein (MAP) kinase signaling by multiple targets in parallel. The authors show that this reporter system is able to detect inhibition of upstream MAP kinase signaling proteins by the MEK inhibitor U0126. The ability to monitor the activity of multiple signaling proteins in a multiwell formal suggests the utility of reverse transfection reporter arrays for high-throughput screening applications.

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