Information
Drawing
Staining
Knowledge
marked
unmarked

Specimen Nr. 02

Specimen:

Hemarthrosis - cartilage (Sheep)

Staining:

SEM

Magnification:

3000x

Important structures :

1.Erythrocytes in fibrin-mesh
2.Fibrin mesh
Das rasterelektronenmikroskopische Präparat zeigt Erythrozyten in einem Netz aus Fibrinfäden. Durch die Interaktion mit dem Fibrinnetz sind die Erythrozyten teils leicht deformiert.

Legende:

Erythrocytes in fibrin-mesh
Fibrin mesh

Scanning electron microscope (SEM)

It is not necessary to prepare ultra-thin sections for examinations under the scanning electron microscope because the electron beam does not penetrate the object, in contrast to transmission electron microscope (TEM).

The SEM image is created directly by a point-to-point visualization of the surface details of the specimen. To achieve this effect, a very thin electron beam scans the surface of the specimen line by line. Each surface point emits secondary electrons whose different intensities are measured by a detector.

When preparing tissue specimens for a scanning electron microscopic examination, the specimens are dried instead of embedded and sliced after fixation and dehydration.

The dehydration technique commonly used today is critical-point drying. The dried specimens are then coated with gold in a vacuum, the so-called sputtering apparatus. This covers the specimen with a surface which can emit secondary electrons.

Ein Thrombus ist ein durch Blutgerinnung intravital entstandenes Blutgerinnsel, vor allem in Gefäßen und an der Herzwand vorkommend. Fibrin bildet das netzartige Gerüst des Gerinnsels, in das weiße und rote Blutzellen eingelagert sind. Zunächst ist der Thrombus von gallertiger Konsistenz, durch Retraktion der Fibrinfäden entsteht dann ein mechanisch stabileres Gebilde.
Home
Tutor
Help
Exit
Boxes
Erythrocytes in fibrin-mesh
Fibrin mesh

HistoNet2000 - Help

1. Organization of the screen surface

Right side: histologic specimen
Left side: information about the specimen (above) and general program functions (below)

2.Histologic specimen

Pull the mouse across the histologic specimen for training purposes. A small square with exclamation marks (dynamic labels) will appear where there is an important structure. You should then decide what structure this could be. To check your result, simply click the appropriate square, and the correct label will appear. The option “marked” allows you to see all labels for all structures simultaneously. These can be removed by clicking “unmarked”. This reactivates the dynamic labels.

3. Complementary information

Info: general information about the specimen, as well as a list of the dynamic labels
Drawing: schematic drawing of the specimen
Staining: information about the staining method for this specimen
Knowledge: short texts with basic histologic information, presently deactivated

4. General Program Functions

Home: returns you to the “start” page
Tutor: how to contact the HistoNet Team
Help: Instructions for Use appear
Exit: closes down the HistoNet program
Boxes: goes back to the other specimen of a topic
VM: provides virtual microscopy

We hope you will enjoy working with HistoNet2000 and learn a lot from it!

Cose help