I've been working for the last 5 years in trying to bring image resolution to «in vivo» imaging comparable to
microscopy because right now we believe there is a disconnect between the clinical imaging that looks at very microscopic features of the eye that are informative of the disease but usually at very late stages and the exquisite work that molecular biologists are doing.
I think I love
microscopy because it integrates art and biology.
Not exact matches
Because they are so small, multiple testing methods are used, including cross-polarized light
microscopy, scanning electron
microscopy and PCR testing of the DNA of larvae in the water sample.
Applying electron
microscopy to biology was a challenge
because the technique is done in a vacuum, which can dry out and distort the shape of proteins and other biological molecules.
This is
because we were using traditional atomic force
microscopy (AFM) techniques, in which the protein - DNA shows up as a single blob, and the DNA path information is missing.»
Because of the way light waves move through hyperbolic metamaterials, they can be used as superlenses to view objects too small to be seen with other
microscopy methods.
Because cement is a heterogeneous material, made up of multiple components, Shahrin used a scanning electron
microscopy / X-ray technique to find the areas in cement samples that had the highest ratio of C - S - H relative to other constituent materials.
Light - sheet
microscopy is appealing
because, by rapidly illuminating one plane after another within a specimen, background haze and light - induced damage are minimized.
Co-author Lisa Tell summarizes: «This study was exciting
because not only were we able to document the presence of a mite on feathers from two species of hummingbirds found in California, but we were also able to examine the positioning of live feather mites in situ with electron
microscopy that is portable enough to use in the field.»
«Nonlinear stage - scanning confocal
microscopy is critical
because it allows us to rapidly measure the nonlinear emission from thousands of different nanostructures while minimizing the potential systematic errors, such as intensity or beam pointing variations, often associated with tuning the wavelength of an ultrafast laser,» O'Brien says.
Marie Trussart, the lead author on the paper, said: «Studying bacteria with such a small genome was a big technical challenge, especially
because we were using super-resolution
microscopy, and it took us five years to complete the project.
«I like it
because you not only can control the viral dose infecting axons but also are able to monitor each step — from transport in axons to expression in the nucleus — by live - cell
microscopy.»
Because these processes are ultimately mechanical in nature, our focus is developing and applying new laser - based optical instrumentation with high - resolution
microscopy imaging to understand cellular mechanics.
«Eggshells are notoriously difficult to study by traditional means,
because they easily break when we try to make a thin slice for imaging by electron
microscopy,» says McKee, who is also a professor in McGill's Department of Anatomy and Cell Biology.
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.
HI lee RN after the ages of 24 to 27 the bodys enzyme production reduces to from a teaspoon to eyedopper levels we start to rely on the bodies own ability to assimilate and absorb its own enzyme source where as we can run through walls at 17 to 27 try to do ot at 37 0r 47 things do nt go as planned recovery takes longer a we age generally with poor diet and junk food shrinkage of organs increase as we age
because of the lack of enzymes that are active in the body fibrin scar tissue and debris as well as sludge in the blood require the following (number 1) is oxygen (number 2) is Enzymes (number 3) is electrolytes (Number 4) is negatively ionized (Red Blood Cells) this is what is required to remove the excessive fibrin from the body Dr perlmutter is correct with his grain and carb theory however without systemic enzyme assistance and the other 3 protocols organ shrinkage and early aging are a reality the enzymes (systemic) do the major work eating up and ridding the excessive fibrin that is in the body and easy to see with
microscopy as is Red Blood cells that are positively ionised (Stuck together) find it had to deliver ATP (cell food) that feed the cells One of the major causes of arterial blockages is inflamation condensed LDL triglycerides (bad cholestorol) not mistaking fluffy or non condensed LDL which is good for the brain and harmless as is HDL cholestorol levels