Which technique would be used to view detailed structures within a cell like mitochondria and ribosomes?

21 Plasma cell View Virtual EM Slide
This electron micrograph shows a typical secretory cell, a plasma cell, which secretes immunoglobulin protein. Many of the major types of cellular organelles are visible in this image. In the nucleus, areas of euchromatin and heterochromatin can easily be identified. Use these micrographs to review the structure of organelles. Be sure you recognise favourable sections of the nucleas, mitochondria, and rough ER.

11 Nuclear Envelope - Transverse Section View Virtual EM Slide
This electron micrograph nicely depicts the double membrane of the nuclear envelope including some nuclear pores.

12 Pancreas Rough ER View Virtual EM Slide
This electron micrograph shows the typical flat cisternae of the rough endoplasmic reticulum, which are studded with ribosomes.

13 Golgi apparatus - Exocrine Pancreas View Virtual EM Slide
The Golgi apparatus looks rather unusual in this electron micrograph. This is due to the enlarged stacks of cisternae (Golgi vacuoles), which distort the appearance of the Golgi complex.

227 Pancreas - Exocrine, detail of acinus Organelles of the Secretory Pathway &View Virtual EM Slide
Pancreatic acinar cells as depicted in this electron micrograph are cells that are highly specialized for protein secretion. Therefore, all the organelles of the protein secretory pathway are well-represented and are clearly visible in this micrograph.

14 Centrioles View Virtual EM Slide
This image shows two centrioles, which represent the central structure of the microtubule-organizing center (MTOC). Some microtubules are also visible in the vicinity.

155 Cilia View Virtual EM Slide
Cross sections of cilia. The typical 9+2 arrangement of the microtubules is especially evident in EM #156.

156 Cilia - Cross-sectioned in human trachea View Virtual EM Slide
Cross sections of cilia. The typical 9+2 arrangement of the microtubules is especially evident. The basal bodies are centrioles and have 9 triplets of microtubules with no central pair.

170 Kidney - Cortex, proximal tuble Brush Border View Virtual EM Slide
This EM micrograph depicts the typical appearance of microvilli on the apical surface of two types of cells with a striated or brush border. Shown is the epithelial lining cell of a proximal tubule in the kidney.

213 Small intestine - microvilli View Virtual EM Slide
Study the typical appearance of microvilli on the apical surface of this cell forming part of the striated or brush border in small intestine.

16 Epithelium - Desmosome and Intermediate Filaments View Virtual EM Slide
A desmosome can be seen in the upper right corner of this transmission electron micrograph. The cytoplasm is full of intermediate filaments (tonofilaments), some of which are attached to the desmosomal plaque.

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Electron microscopy (EM) allows us to observe a world exponentially smaller than the one we can see with our unaided eyes or even with the familiar light microscope. Electron microscopy uses electrons to “see” small objects in the same way that light beams let us observe our surroundings or objects in a light microscope. With EM, we can look at the feather-like scales of an insect, the internal structures of a cell, individual proteins or even individual atoms in a metal alloy.

TEM vs SEM Comparison

The two most common types of electron microscopes are transmission (TEM) and scanning (SEM) systems, but the differences between these two instruments can be fairly nuanced. Here we hope to provide a fundamental primer for individuals looking to get started with this powerful technique.

Scanning Electron Microscope (SEM)

Imagine you are in a dark room with a weak flashlight. To explore your surroundings, you might sweep the light across the room, much like someone reading a book: left to right and top to bottom. SEM functions similarly, sweeping the electron beam across the sample and recording the electrons that bounce back. This technique allows you to see the surface of just about any sample, from industrial metals to geological samples to biological specimens like spores, insects, and cells. While SEM cannot see features to the same level of detail as TEM, it is much faster, less restrictive, and can sometimes be performed with limited or no sample preparation.

Transmission Electron Microscope (TEM)

When a movie plays in the theater, light is transmitted through an image on a film. As the beam of light passes through, it is modified by the image and the contents of the film are then displayed. TEM works in the same way but with electrons,  passing through, or transmitting, an ultrathin sample to a detector below. TEM allows you to observe details as small as individual atoms, giving unprecedented levels of structural information at the highest possible resolution. As it goes through objects it can also give you information about internal structures, which SEM cannot provide. TEM is, however, limited to samples that can be thin enough to let electrons pass through them. This thinning process is technically challenging and requires additional tools to perform.

Which technique would be used to view detailed structures within a cell like mitochondria and ribosomes?

SEM (left) and TEM (right) images of bacteria. Whereas SEM shows numerous bacteria on a surface (green), the TEM image shows the interior structure of a single bacterium.

Overall, TEM offers unparalleled detail but can only be used on a limited range of specimens and tends to be more demanding than SEM. It is important to note that advanced techniques such as cryo-EM, a method which looks at typically biological specimen in a vitrified, amorphous state, have expanded the capabilities of TEM significantly. In particular, biomedical and pharmaceutical research may benefit from the molecular and cellular details that can be revealed by cryo-EM.

In general, if you need to look at a relatively large area and only need surface details, SEM is ideal. If you need internal details of small samples at near-atomic resolution, TEM will be necessary.

Learn more about electron microscopy >>

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Alex Ilitchev, PhD, is a Scientific Content Writer at Thermo Fisher Scientific.

What type of microscope is needed for ribosomes and mitochondria?

Mitochondria are visible with the light microscope but can't be seen in detail. Ribosomes are only visible with the electron microscope.

What type of microscope is used to view mitochondria?

The two primary types of microscopy used for viewing mitochondrial form within cells are light microscopy and electron microscopy (Figure 2), and each hold specific advantages for measuring different structural characteristics (Table 1).

What is a technique that helps reveal structures that can be found within the cell?

Fluorescence microscopy is most often used to detect specific proteins or other molecules in cells and tissues.

What are the techniques used to study cell structure?

Two types of electron microscopy—transmission and scanning—are widely used to study cells. In principle, transmission electron microscopy is similar to the observation of stained cells with the bright-field light microscope.