microscopy

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microscopy

 [mi-kros´kah-pe]
examination with a microscope.
fluorescence microscopy conjugation of antibodies with fluorescent dyes in order to identify specific microorganisms or tissue constituents; see also fluorescence microscopy.
Miller-Keane Encyclopedia and Dictionary of Medicine, Nursing, and Allied Health, Seventh Edition. © 2003 by Saunders, an imprint of Elsevier, Inc. All rights reserved.

mi·cros·co·py

(mī-kros'kŏ-pē),
Investigation of minute objects by means of a microscope.
See also: microscope.
Farlex Partner Medical Dictionary © Farlex 2012

microscopy

The study of a structure using a microscope.
Segen's Medical Dictionary. © 2012 Farlex, Inc. All rights reserved.

mi·cros·co·py

(mī-kros'kŏ-pē)
Investigation of minute objects by means of a microscope.
See also: microscope
Medical Dictionary for the Health Professions and Nursing © Farlex 2012

mi·cros·co·py

(mī-kros'kŏ-pē)
Investigation of minute objects with a microscope.
Medical Dictionary for the Dental Professions © Farlex 2012
References in periodicals archive ?
C-dots have been considered as possible replacements for organic dyes and metallic quantum in bioimaging due to their chemical stability, broad excitation ranges, and excellent fluorescence properties.
Prasad, "High contrast in vitro and in vivo photoluminescence bioimaging using near infrared to near infrared upconversion in [Tm.sup.3+] and [Yb.sup.3+] doped fluoride nanophosphors," Nano Letters, vol.
ZnO NPs exhibit efficient blue emissions and near-UV emissions, which have green or yellow luminescence related to oxygen vacancies, therefore further extending its application into bioimaging field [12,36,120].
Wang, "A fluorescent turn-on probe for highly selective detection of cysteine and its bioimaging applications in living cells and tissues," Sensors and Actuators B: Chemical, vol.
The luminescent property also makes porous silicon an attractive biomaterial in bioimaging. Luminescent porous silicon nanoparticles with emission on 650-900 nm range, fabricated by lifting off porous silicon film and sonication, are suitable candidates for in vivo imaging [45], as like silicon quantum dots, they can be easily degraded in aqueous solutions into non-toxic orthosilicic acid.
The amplified product (905 bp) was electrophoresed in 2% agarose gel stained with ethidium bromide (0.5 [micro]g/ml) and image was documented by gel documentation system (Mini BiS Bioimaging System).
However, a facile and "green" mild process using aqueous medium for the preparation of AgIn[S.sub.2]/polymer nanoconjugates with high luminescent properties (i.e., PL quantum yield, QY > 40%) for augmenting bioimaging sensitivity is beyond the scope of the current study and remains a challenge for the future researches.
Triplet-triplet annihilation has been already applied with success in several research fields, as in luminescence bioimaging [33], photovoltaics [34, 35], and photoinduced drug release [36].
Multiple bioimaging modalities in evaluation of an experimental osteonecrosis induced by a combination of lipopolysaccharide and methylprednisolone.
The results showed that the GQDs could be a promising candidate for bioimaging. Most importantly, compared to the traditional quantum dots (QDs), the GQDs is chemically inert.
He has been Head of Molecular Medicine and Director of the Cell Bioimaging facility at the University of Essex.In 1999 he was awarded the Teaching and Learning Innovation Award by the University of the Essex.
They also speculate on future research and discuss potential developments for their use in sensors, bioimaging, and energy harvesting and conversion.