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Table of Contents

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Table of contents

Table of Contents
Chapter1 .................................................................................................................................................... 2
Tissue Processor: ................................................................................................................................. 2
1.1 Introduction ............................................................................................................................. 2
1.2 Main Functions of a Tissue Processor ..................................................................................... 2
1.3 Main Idea: ................................................................................................................................ 3
1.4 Block diagram .......................................................................................................................... 3
Chapter2 .................................................................................................................................................... 4
electron microscope: ........................................................................................................................... 4
2.1 Function of an Electron Microscope: ....................................................................................... 5
2.2 Main Idea: ................................................................................................................................ 6
Chapter3 .................................................................................................................................................... 7
Autostainer: ........................................................................................................................................... 7
3.1 Function of an Autostainer: ...................................................................................................7
3.2 Main Idea: ............................................................................................................................. 8
Chapter1

Tissue Processor:

1.1 Introduction:

A tissue processor is an essential tool in histopathology labs, used to


prepare biological tissues for microscopic examination. The main goal of
tissue processing is to preserve the tissue structure, remove water, and
replace it with a substance that allows the tissue to be thinly sliced
(sectioned) for analysis.

Figure 1

1.2 Main Functions of a Tissue Processor:

1.2.1 Fixation:

The tissue is immersed in a fixative (often formalin) to preserve its


structure and prevent decomposition.

1.2.2 Dehydration:
Water is gradually removed from the tissue using increasing
concentrations of alcohol (ethanol or isopropanol). This is crucial
because tissues are mostly composed of water, and water needs to be
removed to embed them in paraffin.

1.2.3 Clearing:

The alcohol is then replaced with a clearing agent (usually xylene or


similar) that is miscible with both alcohol and paraffin wax. This step
makes the tissue more transparent and prepares it for infiltration with
paraffin.

1.2.4 Infiltration:

The tissue is infiltrated with melted paraffin wax, replacing the


clearing agent. This allows the tissue to maintain its structure during
sectioning.

1.3 Main Idea:

The tissue processor automates the sequential steps required to prepare


tissue samples for microscopic examination, ensuring that tissues are
adequately preserved, dehydrated, cleared, and embedded in wax. This
process is essential for producing high-quality histological slides, which
are critical for accurate diagnosis and research in pathology.

1.4 Block diagram:

Figure2
Chapter2

electron microscope:

2.1 Introduction:
An electron microscope functions by using a focused beam of electrons
to visualize extremely small structures that cannot be seen with
conventional light microscopes. The main purpose of this device is to
achieve high magnification and resolution, allowing scientists to study the
fine details of cells, microorganisms, materials, and even atomic
structures.

Figure3
2.2 Function of an Electron Microscope:

2.2.1 Magnification:

Electron microscopes provide extremely high levels of


magnification, often up to 2 million times or more. This allows
for detailed examination of specimens at the molecular or even
atomic level.

2.2.2 Resolution:

Because electrons have much shorter wavelengths than visible


light, electron microscopes can achieve resolutions in the range
of 0.1 nanometers. This is thousands of times better than what is
possible with traditional light microscopes.

2.2.3 Imaging:

The microscope uses electromagnetic lenses to focus the


electron beam onto the sample, which interacts with the sample
to produce an image. Depending on the type of electron
microscope (TEM or SEM), the image could show internal
structures or surface features.

2.2.4 Specimen Interaction:

In a Transmission Electron Microscope (TEM), the electron


beam passes through an ultra-thin specimen, creating a 2D
image of internal structures.
In a Scanning Electron Microscope (SEM), the electron beam
scans across the surface of the sample, providing a 3D image of
surface topography.

2.2.5 Sample Preparation:

Specimens must be prepared carefully, as they often need to be


thinly sliced for TEM or coated with a conductive material for
SEM. Additionally, the entire process is carried out in a vacuum
to prevent air molecules from scattering the electrons.

2.3 Main Idea:

The main idea of an electron microscope is to use electron beams instead


of light to magnify and resolve structures at the nanoscale. Its core
function is to reveal extremely fine details of biological, material, and
chemical specimens, far beyond what is possible with light-based
microscopes. This capability is critical in fields like biology,
nanotechnology, materials science, and medical research.

2.4 Block diagram:

Figure4
Chapter3

Autostainer:

3.1 Introduction:
An autostainer is a laboratory device used in histopathology and
immunohistochemistry to automate the staining of tissue samples on
microscope slides. The main purpose of the autostainer is to standardize
and streamline the staining process, improving both consistency and
efficiency when preparing tissue sections for microscopic examination.

Figure5

3.2 Function of an Autostainer:


3.2.1Automated Staining:
The autostainer applies a series of stains and reagents to tissue
slides, following a preset protocol. This eliminates the need for
manual staining, which can be labor-intensive and prone to
variability.

3.2.2Consistent and Reproducible Results:

By automating the process, the autostainer ensures that each


slide is stained uniformly, reducing human error and providing
consistent staining results across multiple samples. This is
critical for diagnostic accuracy in pathology.

3.2.3Multiple Staining Protocols:

Autostainers can be programmed with different staining


protocols depending on the type of analysis required. For
example, in Hematoxylin and Eosin (H&E) staining, the
autostainer first applies hematoxylin to stain the nuclei,
followed by eosin to stain the cytoplasm and other structures.
For immunohistochemistry (IHC), antibodies and other
reagents are applied in sequence.

3.2.4Time-Saving:

The device is designed to handle many slides at once,


significantly reducing the time required to prepare samples
compared to manual methods. This is especially important in
high-throughput labs where many tissue samples need to be
processed quickly.

3.2.5Minimizes Chemical Exposure:

Since the entire process is enclosed within the machine, the


autostainer reduces lab personnel's exposure to potentially
harmful chemicals and reagents used in staining.

3.3 Main Idea:


The main idea of an autostainer is to automate and standardize the
staining of tissue sections on slides, ensuring high-quality, reproducible
results. It increases efficiency, reduces human error, and minimizes
exposure to harmful chemicals, making it essential for laboratories in
pathology, histology, and research that rely on consistent and accurate
tissue staining for diagnosis or analysis.
3.4 Block diagram:

Figure6
Reference

https://www.researchgate.net/

Dako (Agilent Technologies) Autostainer Manual. Available from


Agilent Technologies.

https://www.diapath.com/product/automatic-stainer-giotto-sdsgt9000-
542

https://www.va.gov/DIAGNOSTICEM/What_Is_Electron_Microscopy_and_How_D
oes_It_Work.asp

https://www.umassmed.edu/cemf/whatisem/

1.

1. Carson FL, Cappellano C (2020) Histotechnology: a self-


instructional text, 5th edn. American Society for
Clinical Pathology, Chicago

2.

1. Drury RAB, Wallington EA (1980) Carleton’s histological


technique, 5th edn. Oxford University Press, New York

3.

1. Preece A (1959) A manual for histologic technicians.


Little, Brown and Company, Toronto

4.

1. Lott R, Tunnicliffe J, Sheppard E, Santiago J, Hladik C,


Nasim M et al (2020) Practical guide to specimen handling
in surgical pathology. College of American Pathologists,
Northfield, IL

5.

1. Chapman CM (2019) Troubleshooting in the histology


laboratory. J Histotechnol 42(3):137–149 - DOI

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