3.9 Article

Maximizing RNA Yield from Archival Renal Tumors and Optimizing Gene Expression Analysis

期刊

JOURNAL OF BIOMOLECULAR SCREENING
卷 15, 期 1, 页码 80-85

出版社

SAGE PUBLICATIONS INC
DOI: 10.1177/1087057109355059

关键词

formalin-fixed paraffin-embedded tissues; RNA; TaqMan (R) qPCR

资金

  1. NIH [R01CA133072-01]
  2. NCI [1R21CA121212-01, CA016056]
  3. NATIONAL CANCER INSTITUTE [R21CA121212, P30CA016056, R01CA133072] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Formalin-fixed, paraffin-embedded tissues are widely available for gene expression analysis using TaqMan (R) PCR. Five methods, including 4 commercial kits, for recovering RNA from paraffin-embedded renal tumor tissue were compared. The MasterPure. kit from Epicentre produced the highest RNA yield. However, the difference in RNA yield between the kit from Epicenter and Invitrogen's TRIzol method was not significant. Using the top 3 RNA isolation methods, the manufacturers' protocols were modified to include an overnight Proteinase K digestion. Overnight protein digestion resulted in a significant increase in RNA yield. To optimize the reverse transcription reaction, conventional reverse transcription with random oligonucleotide primers was compared to reverse transcription using primers specific for genes of interest. Reverse transcription using gene-specific primers significantly increased the quantity of cDNA detectable by TaqMan. PCR. Therefore, expression profiling of formalin-fixed, paraffin-embedded tissue using TaqMan. qPCR can be optimized by using the MasterPure. RNA isolation kit modified to include an overnight Proteinase K digestion and gene-specific primers during the reverse transcription. (Journal of Biomolecular Screening 2010: 80-85)

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