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for chemistry, physics and molecular biology. This project takes advantage of how we can combine optical microscopy, single photon counting, and laser fluorescence methods to probe/measure the folding of single
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many different methodological assumptions, that are currently based around simple single conformations of globular proteins. To address this gap, molecular dynamics (MD) simulations and Neutron
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inaccuracies in results. Applicants with experience in molecular biology, qPCR, digital PCR, or next-generation sequencing are encouraged to apply. key words digital pcr; molecular diagnostics; ngs; pcr
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molecular motors and RNA-folding. In a parallel effort, we significantly enhanced the biophysical capabilities of an atomic force microscope (AFM). Specifically, we achieved sub-pN force precision and
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Development of Hyperspectral Raman Imaging for Biology and Medicine: Optical Platform and Data Mining Methods NIST only participates in the February and August reviews. Molecules vibrate with
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extracellular matrix proteins. SPRI sensitivity appears to be uniquely suited to visualize a dynamic range that transitions from the molecular to the macromolecular: specifically the cell contacts with
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for NGS detection of viral adventitious agents. Applicants with experience in molecular biology, qPCR, digital PCR, cell culture, viral propagation, bioinformatics or next-generation sequencing
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measurements are used to monitor these surface and interfacial processes. A primary objective of our research involves characterizing surface and/or molecular chemical and structural characteristics under
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well as at synchrotron radiation facilities. We use ultrathin electron transparent but molecular impermeable membranes made of graphene to isolate the high pressure/liquid sample environment from the high vacuum electron
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trapping of CNTs at polymer/polymer interfaces. This project aims at quantifying these colloidal behaviors in order to achieve fundamental understanding of the underlying molecular forces. Insight gained can