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High Throughput MicroRNA Profiling: Optimized Multiplex qRT-PCR at Nanoliter Scale on the Fluidigm Dynamic ArrayTM IFCs
1The Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research,University of California San Francisco , 2Center for Reproductive Sciences,University of California San Francisco , 3Department of Urology,University of California San Francisco , 4Department of Cell and Tissue Biology,University of California San Francisco , 5Fluidigm Corporation,Fluidigm Corporation , 6Department of Obstetrics and Gynecology,Hadassah-Hebrew University Medical Center, 7UCSF – Helen Diller Family Comprehensive Cancer Center,University of California San Francisco
章
- 00:05標題
- 00:55RNA Concentration
- 02:03Gel Purification of pre-PCR Product
- 03:46Preparing the 96.96 Dynamic Array IFC, the Samples, and the 13x Assays
- 05:25qRT-PCR Analysis of miRNA Expression in Mouse ESC and Human Serum
- 06:10qRT-PCR Analysis
- 07:04Conclusion
Here we describe an optimized multiplex reverse transcriptase quantitative PCR (qRT-PCR) protocol in combination with a microfluidic platform as a cost and time effective high-throughput screening tool for microRNA (miRNA) expression levels, especially when working with limited amounts of sample.
タグ
High Throughput MicroRNA ProfilingMultiplex QRT-PCRFluidigm Dynamic ArrayTM IFCsMiRNAsQuantificationMicroRNA LevelsWild-typeSmall RNA Deficient Mouse Embryonic Stem Cells (mESC)AccuracyRobustnessOptimized MethodPurifying PrimersSingleplex Real-time DetectionMicrofluidic ChipNanoliter VolumesReagent CostsHigh Throughput MiRNA Expression Profiling
