The developed microscopy approach combines two
fluorescence microscopy techniques: REversible Saturable OpticaL Fluorescence Transitions (RESOLFT) Microscopy with reversible switchable fluorescent proteins (RSFPs) and 4Pi - Microscopy.
The developed microscopy approach combines two
fluorescence microscopy techniques: REversible Saturable OpticaL Fluorescence Transitions (RESOLFT) Microscopy and 4Pi Microscopy.
From 2000 to 2003 he was a research scientist at Evotec, Hamburg, developing advanced
fluorescence microscopy techniques for high - throughput drug screening.
Scientists at Albert Einstein College of Medicine of Yeshiva University and their international collaborators have developed a novel
fluorescence microscopy technique that for the first time shows where and when proteins are produced.
Not exact matches
«We use a
technique called scanning X-ray
fluorescence microscopy,» study co-author Satoshi Matsuyama says.
«We applied a new
technique called X-ray
fluorescence microscopy — it looks at elemental composition,» said Marshall.
The
technique, called microenvironmental selective plane illumination
microscopy (meSPIM), uses exceptionally long, thin beams of laser light to trigger
fluorescence in a sample, causing it to glow.
The
technique, called superresolution single - molecule
fluorescence microscopy, recently helped scientists at the University of Manchester in England track natural killer (NK) cells, which help destroy cancer and viruses.
Acquiring images using modern
techniques such as light sheet
fluorescence, confocal, or electron
microscopy creates a significant data stream.
This work, with the assistance of soil scientists at the University of KwaZulu - Natal, has involved a suite of
techniques, including x-ray
fluorescence (to provide quantitative data on minor and trace element composition), x-ray diffraction (to reveal crystal structure and parent rock types of paint ingredients), and environmental scanning electron
microscopy (to yield qualitative data on elements present).
And its ability to show the shape of dendrites and trace neuronal processes provides contextual information unavailable through imaging
techniques such as electron
microscopy,
fluorescence microscopy, and magnetic resonance imaging (MRI).
This new
technique was made possible by the development in recent years of single - molecule
microscopy, which enables scientists to peer into the nano - world by turning the
fluorescence of individual molecules on and off.
A common
technique is
fluorescence microscopy, where fluorescent molecules («probes») are attached to cell structures and then «lit up» against a dark background.
By developing a new
fluorescence microscopy - based
technique, the researchers were able to measure how long it takes proteins to move over distances ranging from 0.2 to 3 micrometres in living cells.
Evidence of the nanoparticles in tumor tissue was found using
fluorescence microscopy, a
technique capable of detecting the chemotherapeutic drug (camptothecin) attached to the nanoparticle.
A number of imaging
techniques will be applied, like
fluorescence microscopy and single - molecule AFM.
Optical imaging and spectroscopy, advanced optical imaging
techniques in particular super-resolution
fluorescence microscopy, optical physics, nanotechnology, single - molecule biophysics and macromolecular biochemistry, single - molecule imaging, gene expression, computational modeling, single - molecule (force) spectroscopy, biomolecular engineering, nucleic acid nanotechnology
Colocalization analysis in
fluorescence microscopy Cell Imaging
Techniques (pp. 97 - 109): Springer.
Fluorescence correlation spectroscopy (FCS) in
microscopy kinetic measurements, principles, analysis and its relation to other photo - kinetic
techniques
Michael Berndt (Diez, MPG)-- «Optical Near - fields in
fluorescence microscopy -
Techniques to access information in the third dimension on the nanometer scale» (2010)
We will continue to study the relationship between the 3D structure and the function of macromolecular complexes using a combination of 3D Electron
Microscopy, Cryo - Electron Tomography, single particle analysis, correlative
fluorescence microscopy, image analysis, and needed biochemical
techniques.
His group focuses on novel
techniques and instrumentation for high - resolution structural and molecular
microscopy based on integrated
fluorescence and electron
microscopy.
We work across disciplines and use a variety of
techniques including microfluidics, standard
microscopies (electron, optical,
fluorescence, confocal), spectroscopies (
fluorescence, UV, CD), scattering
techniques (X-ray, light), protein expression and characterization and cell - free gene expression to investigate the utility of coacervate microdroplets as robust reaction compartments and cellular mimics.
Because electron
microscopy requires objects to be dried and flattened, the researchers used a
fluorescence - based imaging
technique called â $ œDNA PAINTâ $ to visualize the jungle - gym - like structures in solution.
Correlative light and electron
microscopy (CLEM) is an imaging
technique that combines electron
microscopy (EM) with
fluorescence localization data.
The
techniques most widely used in this industry are X-ray diffraction, X-ray
fluorescence microscopy, X-ray Absorption Spectroscopy and X-ray powder diffraction.
Due to its unrivaled contrast,
fluorescence imaging has emerged as the dominant light
microscopy contrast
technique in modern biology (1).
«We applied a new
technique called X-ray
fluorescence microscopy — it looks at elemental composition,» confirmed Marshall.
The projects are multidisciplinary, involving a variety of
techniques including molecular biology (PCR, cloning), cell culture and advanced
fluorescence microscopy.
In cases of neonatal mortality, the diagnosis typically is made postmortem with virus isolation from fresh lung, liver, kidney, and spleen by cell culture
techniques and subsequent identification by PCR and sequencing, transmission electron
microscopy, immunofluorescence, or
fluorescence in situ hybridization.
Proficient with atomic force
microscopy,
fluorescence spectroscopy, protein purification and characterization
techniques.
Professional Duties & Responsibilities Biomedical and biotechnology engineer with background in design of biomaterials, biosensors, drug delivery devices, microfrabrication, and tissue engineering Working knowledge of direct cell writing and rapid prototyping Experience fabricating nanocomposite hydrogel scaffolds Proficient in material analysis, mechanical, biochemical, and morphological testing of synthetic and biological materials Extensive experience in bio-imaging processes and procedures Specialized in mammalian, microbial, and viral cell culture Working knowledge of lab
techniques and instruments including electrophoresis, chromatography,
microscopy, spectroscopy, PCR, Flow cytometery, protein assay, DNA isolation
techniques, polymer synthesis and characterization, and synthetic fiber production Developed strong knowledge of FDA, GLP, GMP, GCP, and GDP regulatory requirements Created biocompatible photocurable hydrogels for cell immobilization Formulated cell friendly prepolymer formulation Performed surface modification of nano - particle fillers to enhance their biocompatibility Evaluated cell and biomaterial interaction, cell growth, and proliferation Designed bench - top experiments and protocols to simulate in vivo situations Designed hydrogel based microfluidic prototypes for cell entrapment and cell culture utilizing computer - aided robotic dispenser Determined various mechanical, morphological, and transport properties of photocured hydrogels using Instron, FTIR, EDX, X-ray diffraction, DSC, TGA, and DMA Assessed biocompatibility of hydrogels and physiology of entrapped cells Evaluated intracellular and extracellular reactions of entrapped cells on spatial and temporal scales using optical, confocal,
fluorescence, atomic force, and scanning electron
microscopies Designed various biochemical assays Developed thermosensitive PET membranes for transdermal drug delivery application using Gamma radiation induced graft co-polymerization of N - isopropyl acylamide and Acrylic acid Characterized grafted co-polymer using various polymer characterization
techniques Manipulated lower critical solution temperature of grafted thermosensitive co-polymer Loaded antibiotic on grafted co-polymer and determined drug release profile with temperature Determined biomechanical and biochemical properties of biological gels isolated from marine organisms Analyzed morphological and mechanical properties of metal coated yarns using SEM and Instron Performed analytical work on pharmaceutical formulations using gas and high performance liquid chromatography Performed market research and analysis for medical textile company Developed and implement comprehensive marketing and sales campaign