UNLOCK THE ANSWERS

TO YOUR LIFE SCIENCE QUESTIONS

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  • TOMOGRAPHY IN SEM
  • High resolution 3D reconstruction
  • Maintains high level of detail through large data set
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Drosophila S2 cells thin section
Sample courtesy of Prof. Benjamin Kapek, Hope College

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Protein labeling, stereocilia and tip links
Courtesy of Corey Lab, Harvard University

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Enterobacteria phage T4

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Penium
Courtesy of Skidmore College

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3View tomography of mouse brain
– Reconstruction of axon and vesicles

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Bacteria

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Zika Virus
Inst. Microbiology/Immunology, Univ. of Ljubljana

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Montage of rabbit retina
Marc Lab, Univ. of Utah

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Human Colonic Mucosa
Janet E. Schwarz, Univ. of Vermont

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Developing spermatids in seminiferous tubule epithelium
Dr. Patrick C. Nahirney, Univ. of Victoria

Life Sciences Applications

download the JEOL CryoNote

On the forefront of a field that advances at an exhilarating speed, researchers in the life sciences need the most powerful instruments available for imaging and analysis at the nanoscale, where life begins and where living organisms interact.

JEOL TEMs are widely used in fields where transmission electron microscopy is an indispensable part of the workflow. In diagnostic work, the lower kV TEMs, such as the JEM-1400, are used to identify pathologies that are crucial for proper treatment of patients. In the QC field, those same TEMs are used for analyzing products in terms of size and/or morphology. In basic research, the TEMs from JEOL are sought after because of their stability and ability to quickly deliver massive amounts of data, such as that used to unravel the connectome. Yet another field is screening for Single Particle Workflows – here samples are evaluated before committing them to hours- or even day-long protocols on high-end, fully automated TEMs such as the JEOL CRYO ARM that can deliver three-dimensional structures of proteins and viruses at (near) atomic detail. Higher kV TEMs, such as the 2100Plus or CRYO ARM 200 are used to enable imaging with higher fidelity. The ultimate TEMs in Life Sciences are those used in cryo-EM.

1.29Å structure of mouse apo-ferritin obtained by Fujita et al. on the CRYO ARM 300 at Spring8 (Japan)
In cryoEM frozen-hydrated samples are imaged using phase contrast without any chemical contrasting agents. The aim of cryoEM is to obtain a structure of a specimen as it exists in vitro, e.g. in a test tube, or in vivo, e.g. a living cell. Understanding the structure of a specimen is key to being able to understand its function. Typically, specimens for cryoEM are flash-frozen using a plunger- or guillotine-like device where they are immersed in a cryogen, such as liquid ethane, liquid propane or a mixture of the two at rates of over 1 m/sec. Essential thinning of the buffer across the grid just prior to flash-freezing is accomplished using blot papers. Alternatives that omit the blotting step have recently come to market. These alternatives also aim at coping with a critical component of the process, which is the air-water interface. The amorphous nature of the water of the cryo specimens requires the grids to be kept below -160ºC at all times, requiring the TEMs to have special remediations to prevent frost from building up on the samples. Every JEOL cryo-TEM has a special designed cryo box to accomplish this crucial task. Thus, samples can be kept frost-free for multiple days. Imaging cryoEM samples is done through low-dose techniques using sophisticated movie-type detectors from Gatan or Direct Electron followed by extensive image processing schemes, such as those in cryoSPARC or Relion. Although cryo-EM has been around since the 1980s, only recently (past 5 years or so) have enormous strides been made understanding issues like beam-induced motion, doming of the ice layer, and charging that have hampered the progress in this field for so many years. The reward of effectively dealing with these issues is obtaining structures of protein complexes at resolutions that allow pertinent questions about function to be raised and answered. The figure shows the 1.29Å structure of mouse apo-ferritin obtained by Fujita et al. on the CRYO ARM 300 at Spring8 (Japan).
The bottom line: for very Life Science Application, there is a JEOL TEM perfectly suited for the job!
JEOL SEMs provide high resolution montages and three-dimensional images of structural details. JEOL FE-SEMs enhance imaging and throughput capabilities with image quality and resolution that rivals a TEM. An ideal tool for research and teaching facilities, the FE-SEM can be equipped with a Transmission Electron Detector, 3View Tomography and other analytical accessories.

JEOL FE-SEMs enhance imaging and throughput capabilities with image quality and resolution that rivals a TEM. An ideal tool for research and teaching facilities, the FE-SEM can be equipped with a Transmission Electron Detector, 3View Tomography and other analytical accessories.

JEOL Mass Spectrometers are used for protein characterization, proteomics, pharmaceuticals, drug development, and high throughput screening.

JEOL NMR spectrometers are used in a broad range of applications, from analysis of molecular structure, dynamics and interactions between various molecules, to fundamental material studies. Those applications are extensively used in many fields and areas, including drug research and development, structural molecular biology, development of battery technologies, food analysis and more.

Neuroscience

SEM for Neuroscience

Electron microscopy is an invaluable tool for mapping the brain for advanced neuroscience studies. The use of STEM-in-SEM (Scanning Transmission Electron Microscopy in a SEM) provides enhanced image contrast at lower voltages making it an excellent method for the characterization of thin sections of brain.

Array Tomography Using Field Emission SEM

  • High lateral resolution images
  • Automatic image acquisition
  • Large volume 3D observation
  • Large area montaging

Serial Block-Face Imaging System

  • Integrated Gatan 3View® System
  • 3D electron microscopy for large volumes

MALDI Imaging

MALDI Imaging with SpiralTOF Mass Spectrometer

  • Imaging and structural analysis of lipids, steroids and drug distribution directly on a brain or spinal tissue
  • Analysis of charge remote fragmentations (CRF), fragmentations particularly informative for lipids, steroids, and peptides
  • Complimentary technique to microscopy
  • 20 micron laser sampling
  • Silver Nano Particle implantation for enhanced, stable imaging
  • 75,000+ high resolution MS imaging with MS/MS confirmation
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