Sentence examples for microscopy methods have from inspiring English sources

Cryogenic microscopy methods have gained increasing popularity, as they offer an unaltered view on the architecture of biological specimens.

Over the last decade, fluorescence microscopy methods have enabled the real-time visualization of single molecules interacting with and transiting through the NPC, allowing novel questions to be examined with nanometer precision.

Standardized test systems such as API® and VITEK® 2 (bioMérieux), or PHOENIX® (BD Diagnostics), complemented by traditional culture and microscopy methods, have so far been used in routine labs for the rapid identification of clinical microorganisms.

Multiphoton and associated microscopy methods have been widely used for imaging dynamic interactions in cells and tissues with submicron resolution [ 1- 3].

In the past decade, the development of new fluorescence microscopy methods has revolutionized how biologists use light microscopes to study cellular structure.

Super-resolution microscopy (SRM) methods have allowed scientists to exceed the diffraction limit of light, enabling the discovery and investigation of cellular structures at the nanometer scale, from individual proteins to entire organelles.

Scanning electron microscopy and electrochemical methods have been used to characterize the MWCNTs/PoAP nanocomposite film.

AO has proven effective to improve the signal and the resolution of images in a number of imaging modalities and most notably in nonlinear microscopy, where several methods have been developed for measuring aberrations [ 1, 2, 3, 4, 5, 6].

Microscopy and chromosome capture methods have revealed a hierarchical organisation into territories, domains and subdomains that ensure the accessibility of expressed genes and eventually chromatin loops that serve to bring gene enhancers into proximity of their target promoters.

Due to the potential for rapid and serious disease progression, direct parasite detection by stained blood smears and light microscopy or DNA-based methods have traditionally been used for the diagnosis of acute infections.

Such methods were initially used only for immunoelectron microscopy; however, over time, these methods have been used for additional applications in passive agglutination tests, light microscopy staining, immunoblotting, immunoblot filtration assays, and immunoassays [ 5– 7].