Ion beam pulsing for time of flight (TOF) experiments

1985 ◽  
Vol 18 (1) ◽  
pp. 17-19 ◽  
Author(s):  
D Rathmann ◽  
N Exeler ◽  
B Willerding
Keyword(s):  
Ion Beam ◽  
1967 ◽  
Vol 14 (3) ◽  
pp. 174-180 ◽  
Author(s):  
K. H. Purser ◽  
A. Bahnsen ◽  
M. S. Krick

2021 ◽  
Author(s):  
Marc MB Bosse ◽  
Sean Bendall ◽  
Mike Angelo

This protocol is the standard FFPE tissue staining procedure recommended for Multiplex Ion Beam Imaging Time of Flight instrument (MIBI_TOF) developed in the Sean C. Bendall and Michael R. Angelo labs. The protocol has been successfully used for MIBI and is the result of extensive optimization experiments. It is inspired from state-of-the art of immunohistochemistry staining procedures but differs in some very important steps, namely, glutaraldehyde fixation and final washes prior tissue dehydration. Failure to follow exactly all steps described in this procedure may result in inconsistencies in output data after MIBI_TOF acquisition.


2019 ◽  
Vol 12 (8) ◽  
pp. 085005
Author(s):  
Kosuke Nagata ◽  
Ken-ichi Bajo ◽  
Satoru Itose ◽  
Miyuki Matsuya ◽  
Morio Ishihara ◽  
...  

2019 ◽  
Vol 5 (10) ◽  
pp. eaax5851 ◽  
Author(s):  
Leeat Keren ◽  
Marc Bosse ◽  
Steve Thompson ◽  
Tyler Risom ◽  
Kausalia Vijayaragavan ◽  
...  

Understanding tissue structure and function requires tools that quantify the expression of multiple proteins while preserving spatial information. Here, we describe MIBI-TOF (multiplexed ion beam imaging by time of flight), an instrument that uses bright ion sources and orthogonal time-of-flight mass spectrometry to image metal-tagged antibodies at subcellular resolution in clinical tissue sections. We demonstrate quantitative, full periodic table coverage across a five-log dynamic range, imaging 36 labeled antibodies simultaneously with histochemical stains and endogenous elements. We image fields of view up to 800 μm × 800 μm at resolutions down to 260 nm with sensitivities approaching single-molecule detection. We leverage these properties to interrogate intrapatient heterogeneity in tumor organization in triple-negative breast cancer, revealing regional variability in tumor cell phenotypes in contrast to a structured immune response. Given its versatility and sample back-compatibility, MIBI-TOF is positioned to leverage existing annotated, archival tissue cohorts to explore emerging questions in cancer, immunology, and neurobiology.


2020 ◽  
Vol 4 (4) ◽  
pp. 40
Author(s):  
Keisuke Yasuda

The time-of-flight elastic recoil detection analysis (TOF-ERDA) method is one of the ion beam analysis methods that is capable of analyzing light elements in a sample with excellent depth resolution. In this method, simultaneous measurements of recoil ion energy and time of flight are performed, and ion mass is evaluated. The energy of recoil ions is calculated from TOF, which gives better energy resolution than conventional Silicon semiconductor detectors (SSDs). TOF-ERDA is expected to be particularly applicable for the analysis of light elements in thin films. In this review, the principle of TOF-ERDA measurement and details of the measurement equipment along with the performance of the instrumentation, including depth resolution and measurement sensitivity, are described. Examples of TOF-ERDA analysis are presented with a focus on the results obtained from the measurement system developed by the author.


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