Literature DB >> 15961230

Phase contrast and DIC illumination for AFM hybrids.

Robert A Lugmaier1, Thorsten Hugel, Martin Benoit, Hermann E Gaub.   

Abstract

High-resolution optical microscopy is an essential pre-requisite for life science force microscopy, particularly for applications in cell biology and medicine. Identification and validation of cells is typically established with techniques like phase contrast microscopy or differential interference contrast microscopy. The option to select or monitor individual cells online with such light microscopy techniques while performing atomic force microscopy (AFM) measurements is therefore extremely beneficial. Here, we report two conceptually different strategies to implement these light microscopy techniques in a fully functional AFM head at the ultimate resolution of the Abbe diffraction limit.

Mesh:

Year:  2005        PMID: 15961230     DOI: 10.1016/j.ultramic.2005.04.008

Source DB:  PubMed          Journal:  Ultramicroscopy        ISSN: 0304-3991            Impact factor:   2.689


  3 in total

1.  Dynamic restacking of Escherichia coli P-pili.

Authors:  Robert A Lugmaier; Staffan Schedin; Ferdinand Kühner; Martin Benoit
Journal:  Eur Biophys J       Date:  2007-06-07       Impact factor: 1.733

2.  Label-free optical imaging of membrane patches for atomic force microscopy.

Authors:  Allison B Churnside; Gavin M King; Thomas T Perkins
Journal:  Opt Express       Date:  2010-11-08       Impact factor: 3.894

3.  Condenser-free contrast methods for transmitted-light microscopy.

Authors:  K F Webb
Journal:  J Microsc       Date:  2014-09-16       Impact factor: 1.758

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.