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Life Sciences

FEI electron microscopy solutions are being used today in research laboratories around the world: to explore the in vivo molecular mechanisms of disease; to visualize the 3D architecture of tissues and cells; to unambiguously determine the conformation of flexible protein structures and complexes; and to observe individual viruses and macromolecular complexes in their natural biological context.

Learn more about FEI Solutions for Life Sciences in the video below.

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Scanning Electron Microscopes (SEM)
SEM
Transmission Electron Microscopes (TEM)
TEM
DualBeam Microscopes
DualBeam™­
Focused Ion Beam Microscopes
FIB
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Structural Biology

Structural Biology
Today, cryo electron microscopy (EM) and more specifically single particle analysis has become a powerful tool in determining the 3D structure of macromolecules and macromolecular complexes at subnanometer resolution.  If well-ordered, helical or 2D crystalline specimens are available, near-atomic resolution can be achieved and the biological function of the studied molecule can be understood in atomic detail. The resolution on structures like these have been significantly improved over the last couple of years down to the sub 3A level. Although it is difficult to recognize individual amino acid residues at this resolution, researchers can derive important information regarding protein domain arrangements or can even be able to trace the polypeptide side chains and aromatic rings.

The combination of EM reconstruction with X-ray crystallography and NMR spectroscopy enables structural biologists to gain a much more comprehensive understanding of the studied molecule than could possibly be achieved with any single technique.  EM reconstruction can be interpreted in greater precision by fitting an X-ray model into an EM density map.  On the other hand, an EM reconstruction at low resolution (20 Å) can be used as a phasing model in solving crystallographic structures of viruses or macromolecules.

Providing an automated workflow from sample preparation, to image acquisition and reconstruction, to visualization - FEI Structural Biology solutions provide insight into the architecture and shape of macromolecular complexes and their functions.

Cellular Biology

Cellular Biology
FEI Cellular Biology solutions provide insight on the activities, functions, properties and organization of cells and a deeper understanding of the three-dimensional organization and function of cells. Dehydrating a cell for study can significantly alter the results of the investigation. High-resolution microscopy allows unique imaging of cell membrane structures and sub-cellular morphology in fully hydrated conditions. Biological samples can be quickly fixed by a cryo sample preparation device and subsequent automated cryo-fracture techniques allow further study of interior cellular structures.

Systems Biology

Tissue Biology
Tissue Biology provides insight on the interactions between the components of biological systems and how these interactions give rise to the function and behavior of that system. The aim is to explain biological regulation at a cellular, tissue, organ, or whole organism level in order to understand living systems as a whole. To do this effectively, biological data needs to be collected, interpreted, and analyzed at a level above its individual role in specific cellular mechanisms, compartments, or components. FEI provides automated solutions which quickly enable high resolution ultrastructural imaging over large areas and volumes of tissues or cells.

Biomaterials

Biomaterials
Ultrastructural imaging techniques serve an increasingly essential role in the rigorous characterization of engineered tissues and biomaterials. There is a clear need to understand not only what chemical and biological species are present in a biomaterial but how those species are spatially distributed and how long they remain functional. Recent advances have extended the application of 2D and 3D electron microscopy imaging technologies to reveal complex biological events and species at biomaterial–tissue interfaces. The ability to probe such interactions is tremendously valuable to investigators seeking to design improved biomaterials with enhanced functionality and specificity.

Nanoparticle-based drug delivery, particularly polymeric particle systems wherein delivery is achieved by encapsulation, or physical entrapment, of a drug within the particle matrix, has been a very active area of interest that has resulted in several successful products. The important technological advantages of nanoparticles used as drug carriers are high stability, high carrier capacity, feasibility of incorporation of both hydrophilic and hydrophobic substances, and feasibility of variable routes of administration, including oral application and inhalation. Nanoparticles can also be designed to allow controlled (sustained) drug release from the matrix. The properties of nanoparticles are highly dependent on their consistent formation and loading, which can be easily visualized using electron microscopy.

FEI solutions in Biomaterials enable the visualization of molecular, cellular, and tissue level interactions with biomaterial surfaces and the characterization of nanoparticle drug delivery systems.

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Structural Biology

  • Cryo fixation
  • Dual-axis tomography
  • Single particle analysis
  • Template matching
  • 2D electron crystallography
  • Electron tomography

Cellular Biology

Tissue Biology

  • 3D tissue imaging
  • Biological pathways
  • Biomarkers
  • Cellular organization and morphology

Biomaterials

Brochures: Datasheets: Application Notes & Whitepapers: Case Studies: Articles & Abstracts: Miscellaneous:

Events for Life Sciences


EventEvent TypeDateLocation
EMBO Cryo-EM and Image Processing CourseConference2012-08-26Heidelberg, Germany
Microscopy & Microanalysis 2012Conference2012-07-29Phoenix, Arizona
Structural Biology International Conference on Structural Analysis of Supramolecular Assemblies by Hybrid MethodsConference2012-03-14Lake Tahoe, California
Cellular Biology Future Challenges in Integrative Structural BiologyConference2012-05-24Strasbourg, France
Structural Biology GRC Three Dimensional Electron Microscopy Conference2012-05-27Les Diablerets, Switzerland
Cellular Biology European Light Microscopy Initiative (ELMI) Meeting Conference2012-06-05Leuven, Belgium
Cellular Biology EMBO Tomography Workshop Conference2012-06-18Leiden, The Netherlands
Cellular Biology Correlative Light Electron Microscopy Workshop Conference2012-07-15Bristol, UK
Cellular Biology International Congress of Histochemistry and Cytochemistry Conference2012-08-26Kyoto, Japan
Structural Biology K. H. Kuo Summer School of Electron Microscopy and Crystallography Conference2012-09-07Heifei/Huangshan, China
European Microscopy Congress - EMC 2012Conference2012-09-21Manchester, UK
Structural Biology Biophysical Society of JapanConference2012-09-22Nagoya, Japan
Tissue Biology NeuroscienceConference2012-10-13New Orleans, Louisiana
Structural Biology Scripps Cryo-EM WorkshopConference2012-11-01San Diego, California
Cellular Biology American Society for Cell Biology (ASCB) Conference2012-12-15San Francisco, California
Correlative light and electron microscopy: different flavorsWebinar2012-05-29Webinar

Life Sciences Images

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Magellan XHR SEM

Magellan XHR Image

Work Flow Solution for Life Sciences

The Magellan™ extreme-resolution SEM can resolve nanometer-scale detail on biological specimens with minimal artifacts from beam damage or sample preparation, and features a fully integrated workflow that boosts laboratory productivity and expedites discovery.

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Atomic Model of Virus Reveals Mechanism Used to Economically Carry Out Conserved Functions

Cytoplasmic Virus

Unlike the multishelled viruses in the Reoviridae, cytoplasmic polyhedrosis virus (CPV) is single shelled, yet stable and fully capable of carrying out functions conserved within Reoviridae. In this article, which appears in Structure Magazine, it is revealed how CPV proteins have evolved in a coordinative manner to economically carry out their conserved functions. 

Download the complete article