Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Jan Philipp Eberle"'
Autor:
Manuel Gunkel, Jan Philipp Eberle, Ruben Bulkescher, Jürgen Reymann, Inn Chung, Ronald Simon, Guido Sauter, Vytaute Starkuviene, Karsten Rippe, Holger Erfle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ba7246cdaed5070e579e13ce9bb7dbd
https://doi.org/10.1017/9781108525909.006
https://doi.org/10.1017/9781108525909.006
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 1663
Single-molecule localization microscopy (SMLM) enables imaging of biological structures in the nanometre range. Long measurement times are the consequence of this kind of microscopy due to the need of acquiring thousands of images. We built a setup t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::099ffb4e9e5969f9e49ad128d45cef32
https://pubmed.ncbi.nlm.nih.gov/28924665
https://pubmed.ncbi.nlm.nih.gov/28924665
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 1563
Applying the right acquisition method in a fluorescence imaging-based screening context is of great importance to obtain an appropriate readout and to select the right scale of the screen. In order to save imaging time and data, we have developed rou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8b7287b0d5156b747c94d96aa59630e1
https://pubmed.ncbi.nlm.nih.gov/28324614
https://pubmed.ncbi.nlm.nih.gov/28324614
Autor:
Holger Erfle, Alexander Rapp, Jan Philipp Eberle, Manuel Gunkel, Matthias Krufczik, Marion Eryilmaz, Michael Hausmann
Publikováno v:
Methods in Molecular Biology ISBN: 9781493972647
Fluorescence microscopy is an essential tool for imaging tagged biological structures. Due to the wave nature of light, the resolution of a conventional fluorescence microscope is limited laterally to about 200 nm and axially to about 600 nm, which i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6b34a4456543c6ec5833697b7134424
https://doi.org/10.1007/978-1-4939-7265-4_1
https://doi.org/10.1007/978-1-4939-7265-4_1
Publikováno v:
Methods in Molecular Biology ISBN: 9781493968084
Applying the right acquisition method in a fluorescence imaging-based screening context is of great importance to obtain an appropriate readout and to select the right scale of the screen. In order to save imaging time and data, we have developed rou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d56253765622c7f94182ec034f45fd5
https://doi.org/10.1007/978-1-4939-6810-7_17
https://doi.org/10.1007/978-1-4939-6810-7_17
Publikováno v:
Methods in Molecular Biology ISBN: 9781493972647
Single-molecule localization microscopy (SMLM) enables imaging of biological structures in the nanometre range. Long measurement times are the consequence of this kind of microscopy due to the need of acquiring thousands of images. We built a setup t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2608125761885745530f6a34994c6fb0
https://doi.org/10.1007/978-1-4939-7265-4_12
https://doi.org/10.1007/978-1-4939-7265-4_12
Autor:
Malte Kriegs, Christoph Cremer, Nina Struve, Jan Philipp Eberle, Florian Schock, Margund Bach, Philip S. Boyd, Martin Gote, Michael Hausmann
Publikováno v:
Nanoscale. 8(48)
For receptor tyrosine kinases supramolecular organization on the cell membrane is critical for their function. Super-resolution fluorescence microscopy techniques have offered new opportunities for the analysis of single receptor localization. Here,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4e9be4a2fb02ec43316b069cc230486
https://pubmed.ncbi.nlm.nih.gov/27883139
https://pubmed.ncbi.nlm.nih.gov/27883139