We demonstrate interferometric scattering (iSCAT) microscopy, a method capable of detecting single unlabeled proteins secreted from individual living cells in real time. In this protocol, we cover the fundamental steps to realize an iSCAT microscope and complement it with additional imaging channels to monitor the viability of a cell under study. Following this, we use the method for real-time detection of single proteins as they are secreted from a living cell which we demonstrate with an immortalized B-cell line (Laz388). Necessary steps concerning the preparation of microscope and sample as well as the analysis of the recorded data are discussed. The video protocol demonstrates that iSCAT microscopy offers a straightforward method to stu...
Current in vitro optical studies of microtubule dynamics tend to rely on fluorescent labeling of tub...
Fluorescence microscopy has been the workhorse for investigating optical phenomena at the nanometer ...
ABSTRACT: Optical detection of individual proteins requires fluorescent labeling. Cavity and plasmon...
Cellular secretion of proteins into the extracellular environment is an essential mediator of critic...
Cellular secretion of proteins into the extracellular environment is an essential mediator of critic...
Interferometric scattering microscopy (iSCAT) is an extremely sensitive imaging method based on the ...
Detection of single analyte molecules without the use of any label would improve the sensitivity of ...
The mobility of proteins and lipids within the cell, sculpted oftentimes by the organization of the ...
Interferometric scattering (iSCAT) microscopy is a powerful tool for label-free sensitive detection ...
It has been shown that interferometric detection of Rayleigh scattering (iSCAT) can reach an exquisi...
Bright-field light microscopy and related techniques continue to play a key role in life sciences be...
Interferometric scattering microscopy (iSCAT) is a light scattering-based imaging modality that offe...
Interferometric scattering microscopy (iSCAT) has emerged in recent years as a highly sensitive imag...
Microscopy based on the interferometric detection of light scattered from nanoparticles (iSCAT) was ...
Optical microscopes have for centuries been our window to the microscopic world. The advent of singl...
Current in vitro optical studies of microtubule dynamics tend to rely on fluorescent labeling of tub...
Fluorescence microscopy has been the workhorse for investigating optical phenomena at the nanometer ...
ABSTRACT: Optical detection of individual proteins requires fluorescent labeling. Cavity and plasmon...
Cellular secretion of proteins into the extracellular environment is an essential mediator of critic...
Cellular secretion of proteins into the extracellular environment is an essential mediator of critic...
Interferometric scattering microscopy (iSCAT) is an extremely sensitive imaging method based on the ...
Detection of single analyte molecules without the use of any label would improve the sensitivity of ...
The mobility of proteins and lipids within the cell, sculpted oftentimes by the organization of the ...
Interferometric scattering (iSCAT) microscopy is a powerful tool for label-free sensitive detection ...
It has been shown that interferometric detection of Rayleigh scattering (iSCAT) can reach an exquisi...
Bright-field light microscopy and related techniques continue to play a key role in life sciences be...
Interferometric scattering microscopy (iSCAT) is a light scattering-based imaging modality that offe...
Interferometric scattering microscopy (iSCAT) has emerged in recent years as a highly sensitive imag...
Microscopy based on the interferometric detection of light scattered from nanoparticles (iSCAT) was ...
Optical microscopes have for centuries been our window to the microscopic world. The advent of singl...
Current in vitro optical studies of microtubule dynamics tend to rely on fluorescent labeling of tub...
Fluorescence microscopy has been the workhorse for investigating optical phenomena at the nanometer ...
ABSTRACT: Optical detection of individual proteins requires fluorescent labeling. Cavity and plasmon...