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  1. ...increase to hundreds of millions of indi- vidual reactions per year. Nucleic Acid Analysis is Consistent and Amenable to Automation The biochemistries for extracting nucleic acid infor- mation are relatively uniform. Samples are aqueous and within a defined range of volume (1 ml-0.1 lJl), temperature (0°C...
  2. ...that is coupled to a multicolor detection system capable of single-fluorophore sensitivity. Double-stranded DNA molecules were tagged at sequence-specific motif sites with fluorescent bisPNA (Peptide Nucleic Acid) tags. The DNA molecules were then stretched in the microfluidic device and driven in a flow stream...
  3. ...as they require sophisticated custom-made equipment and in-depth microfluidic and ChIP expertise, while lacking parallelization. To enable standardized, automated ChIP-seq profiling of low-input samples, we constructed microfluidic PDMS-based plates capable of performing 24 sensitive ChIP reactions within 30 min...
  4. .... The embryos were dissociated and cross-linked as described above, and ChIP was performed with the true MicroChIP kit (Diagenode). Primer sequences for qPCR are provided in the Supplemental Table S3. H3K9me2 ChIP-seq ChIPwas performed as described above on three pools of eight embryos collected at E8.5. Ch...
  5. .... 32 : W176 – W180 . ↵ Rychlik W. , Spencer W.J. , Rhoads R.E. ( 1990 ) Optimization of the annealing temperature for DNA amplification in vitro. Nucleic Acids Res. 18 : 6409 – 6412 . ↵ Sharp P.M. , Cowe E. , Higgins D.G. , Shields D.C. , Wolfe K.H. , Wright F. ( 1988 ) Codon usage patterns...
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  6. .... Caged RNA: Photo-control of a ribozyme reaction. Nucleic Acids Res. 26 : 3173 -3178. ↵ Collins, F. and Galas, D. 1993 . A new five-year plan for the U.S. Human Genome Project. Science 262 : 43 -46. ↵ Collins, F.S., Guyer, M.S., and Chakravarti, A. 1997 . Variations on a theme: Cataloging human DNA...
  7. .... Biol. Chem. 265 : 7576 – 7582 . ↵ Gilles P.N. , Wu D.J. , Foster C.B. , Dillon P.J. , Chanock S.J. ( 1999 ) Single nucleotide polymorphic discrimination by an electronic dot blot assay on semiconductor microchips. Nature Biotechnol. 17 : 365 – 370 . ↵ Goodfriend T.L. , Elliott M.E. , Catt K.J. ( 1995...
  8. .... ↵ Yuen P.-K. , Kricka L.J. , Fortina P. , Panaro N.J. , Sakazume T. , Wilding P. ( 2002 ) Microchip module for blood sample preparation and nucleic acid amplification reactions. Genome Res. 11 : 405 – 412 . ↵ Zarrinkar P.P. , Mainquist J.K. , Zamora M. , Stern D. , Welsh J.B. , Sapinoso L.M. , Hampton G...
  9. ...capture-oligo for each targeted MIR that is covalently coupled onto color-coded microspheres (beads), and a detection-oligo that is labeled with biotin ( Fig. 4 ). Both capture and detection oligos are spiked with Locked Nucleic Acid (LNA) nucleotides to increase specificity and sensitivity ( Petersen...
  10. ...performed ChIP assays using antibodies to E2F4, H3me3K27, H3me3K9, and 5-MeC (two independent ChIP assays were performed for each antibody), prepared amplicons, and analyzed the samples using ENCODE arrays that represent 44 regions (∼1% of the human ) ranging from 500 kb to 2 Mb. We first identified 116 E2F...
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