Single-cell study of the extracellular matrix effect on cell growth by in situ imaging of gene expression† †Electronic supplementary information (ESI) available: Sequence information, in vitro RCA and RT-qPCR data. See DOI: 10.1039/c7sc03880a
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چکیده
1. Experimental Procedures S2 2. Figure. S1. Target DNA assay by RCA in vitro. S4 3. Figure. S2. Quantitative detection of the target sequence in vitro. S5 4. Figure. S3. Quantitative detection of real mRNA GAPDH by RCA in vitro. 5. Figure. S4. Identification of RCA amplicons in the fluorescence image. S5 S6 6. Table S1. PAAm Hydrogel mechanical and swelling properties after polymerization of relative acrylamide and bis-acrylamide concentration. S7
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Simultaneous visualization of the subfemtomolar expression of microRNA and microRNA target gene using HILO microscopy† †Electronic supplementary information (ESI) available: The LED device for the sample photobleaching, a schematic presentation of HILO microscopy, fluorescence spectra and hybridization curves of the molecular beacons, the linear correlation between the miRNA fluorescence intensity and the miRNA copy number, a validation of the miRNA adsorption and miRNA target gene expression via RT-qPCR, a validation of RT-qPCR using capillary electrophoresis, the reproducibility of RT-qPCR and Poisson distribution of the miRNA pipetting as well as a complete list of the oligonucleotides used in this study. See DOI: 10.1039/c7sc02701j Click here for additional data file.
Department of Chemistry, Tunghai Univ [email protected] Graduate Institute of Oncology, College o Taipei 100, Taiwan Department of Internal Medicine, National Taiwan Department of Oncology, National Taiwan † Electronic supplementary information sample photobleaching, a schematic uorescence spectra and hybridization linear correlation between the miRNA copy number, a validation of the miRN ex...
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