Skip to main content

Introduction To Microscope-Defination,Types,Parts,Drawing,Diagram

Introduction To Microscope-Defination,Types,Parts,Drawing,Diagram

INTRODUCTION TO MICROSCOPE:
A microscope (from the Greek: mikrós, "small" and skopeîn, "to look" or "see") is an instrument used to see objects that are too small for the naked eye.
MICROSCOPY:
The science of investigating small objects using such an instrument is called microscopy.Microscopic means invisible to the eye unless aided by a microscope. 
MAGNIFICATION:
For calculation of the total magnification when viewing an image with a light microscope, first take the power of the objective lens which is at 4x, 10x or 40x and then multiply it by the power of the eyepiece which is generally 10x. It means, a 10x eyepiece used with a 40x objective lens, will produce a magnification of 400x. Magnification is a measure of increase in diameter of an object.
RESOLUTION:
Resolution means the degree of detail. Resolving Power may be described as the ability to measure the separation of images that are close together. The shorter wavelength ensures increased resolution.
PRINCIPLE OF WORKING:
MAGNIFICATION SYSTEM:

Stereo microscopes have two major types of magnification systems. One fixed magnification and other zoom magnification. Primary magnification is a part of fixed magnification which is achieved by set of objective lenses with a set degree of magnification. While with Zoom magnification, range of magnification is already set and magnification can be continuously changed within that range. If one wants more magnification of the object, it can be achieved by using auxiliary objectives that increase total magnification by a set factor. By changing the eyepiece, one can increase or decrease total magnification of both fixed and zoom system. In between these two magnifications, there are fixed-focus convex lenses that are arranged so to achieve the fixed magnification. This system is called "Galilean optical system". But the difference to fixed magnification is that if same arrangement of these convex lenses is physically inverted one will get the different magnification. So to get two different magnifications, same set of lenses can be used; two sets of lenses will provide four magnifications and so on. Galilean optical system is a good replacement of expensive zoom magnification system.
ILLUMINATION:
Introduction To Microscope-Defination,Types,Parts,Drawing,Diagram

Fiber optic light source with halogen lamps is used to illuminate specimen which gives high light output for a given power input. Many other light stalks are also used for the same specimen, so increasing the illumination yet further.
VIEWING HEADS:
1. MONOCULAR 2. BINOCULAR 3. TRINOCULAR
1. MONOCULAR
The use of only one eyepiece when viewing the specimen. The monocular microscopes are light weight and inexpensive.
2. BINOCULAR
A microscope having two eyepieces. It is most comfortable to use as a common choice.
3. TRINOCULAR
It has a third eyepiece tube that can be used by another person simultaneously or by a CCD camera. The trinocular option is more expensive than monocular or binocular.
TYPES OF MICROSCOPES

  • Simple Microscope: Simple microscope is first developed microscope by Antony van Leeuwenhoek in 17th century. It was prepared by convex lens with specimen holder with 200 to 300 time magnifications. Now a day this microscope is not used commonly because of availability of more advanced microscopes.

Introduction To Microscope-Defination,Types,Parts,Drawing,Diagram


  • Compound Microscopes: Compound microscope has two lens so it provides batter magnification compered to simple microscope. This is also called bright field microscope because light is under the specimen. Compound microscopes can be mono or binocular. It can magnify specimen up 1000 times. These microscopes are relatively inexpensive that’s why they are used everywhere.
  • Stereo Microscope: The stereo microscope, also called a dissecting microscope, provides magnification of up to 300 times. These binocular microscopes are used to look at opaque objects or objects that are too large to be viewed with a compound microscope, since they do not require a slide preparation. Although their magnification is relatively low, they are still useful. They provide a close-up, 3-D view of objects’ surface textures, and they allow the operator to manipulate the object during viewing.

Introduction To Microscope-Defination,Types,Parts,Drawing,Diagram


  • Confocal Microscope: Unlike stereo and compound microscopes, which use regular light for image formation, the confocal microscope uses a laser light to scan samples that have been dyed. These samples are prepared on slides and inserted; then, with the aid of a dichromatic mirror, the device produces a magnified image on a computer screen. Operators can create 3-D images, as well, by assembling multiple scans.

Introduction To Microscope-Defination,Types,Parts,Drawing,Diagram


  • Scanning Electron Microscope (SEM) The scanning electron microscope, or SEM, uses electrons rather than light for image formation. Samples are scanned in vacuum or near-vacuum conditions, so they must be specially prepared by first undergoing dehydration and then being coated with a thin layer of a conducive material, such as gold. After the item is prepared and placed in the chamber, the SEM produces a 3-D, black-and-white image on a computer screen.
  • Transmission Electron Microscope (TEM)Like the scanning electron microscope, the transmission electron microscope (TEM) uses electrons in creating a magnified image, and samples are scanned in a vacuum so they must be specially prepared. Unlike the SEM, however, the TEM uses a slide preparation to obtain a 2-D view of specimens, so it's more suited for viewing objects with some degree of transparency. A TEM offers a high degree of both magnification and resolution, making it useful in the physical and biological sciences, metallurgy, nanotechnology and forensic analysis.
CARE AND WISE USE OF MICROSCOPES:
  1. Ever hold a microscope firmly by the stand, only. Don’t catch it by the eyepiece holder.
  2. When to unplug the illuminator; hold the plug (not the cable).
  3. After completion of lab work, turn the illuminator off.
  4. The stage and lenses should be cleaned before putting away the microscope.
  5. Always use a good quality lens tissue or a cotton swab (100% natural cotton) to clean an optical surface. Appropriate lens cleaner or distilled water may be used to help remove dried material. Organic solvents will damage the lens coatings.
  6. Cover the microscope with a dust cover when it is not in use.
  7. Try to focus smoothly and lightly. Increased resistance during focusing shows that you have reached a limit. 
------------------------------------------------------------------------------------------
Here You Can Find Plant Disease and Pathogens (Fungi, Bacteria, Molllicutes, Parasitic higher plants, Parasitic Green Algae, Nematodes, Protozoa, Viruses, Viroids,Prions) Diagnosis and Treatment, Control Against Plant Disease. Laboratory Experiments & Work. Plant Pathology Lab Manual. House Plant-Trees Care Guide, Snake Plant Care, Pothos Plant Care, Plant Care for dummies, Plant Care  Printable, Products, Plant Care Tips, Symbols, Tags, Database, Careers, Websites, Apps & Card.
Written By:
Dr.Qaiser Shakeel
Tahir Mahmood
Department of Plant Pathology-Agriculture
The Islamia University of Bahwalpur-Pakistan.

Comments

Popular posts from this blog

Preparation of Media For Culture-PDA, PDB & NA Recipes

PREPARATION OF MEDIA FOR CULTURE: Media play an important role not only for the nutrition and growth of the pathogen but also in identification through growth pattern on media. Fungi and Bacteria need synthetic media enriched with essential element for the growth. In general different types of media are prepared to culture fungi and bacteria but Potato dextrose agar (PDA) for fungi and Nutrient agar for bacteria are being used commonly.  RECIPES OF DIFFERENT MEDIA: POTATO DEXTROSE AGAR: Potato Starch 250  mL/15g Dextrose-15g Agar -Agar 15g Distilled water  750 mL/1000mL PROCEDURE TO PREPARE POTATO DEXTROSE AGAR MATERIAL: Petri dish, Flask, test tubes, Agar-agar, Dextrose, Potato starch, Water PROCEDURE: First of all take potatoes to extract potato starch. Peel the potatoes and cut into small pieces. Preferably 200 g of potato pieces are weighed, washed quickly in running water, placed in 1l liter of water and boiled for nearly

GEL Procedure Of Gel Electrophoresis For Separation DNA/RNA

GEL Procedure Of Gel Electrophoresis For Separation-DNA/RNA GEL ELECTROPHORESIS GEL Procedure Of Gel Electrophoresis For Separation-DNA/RNA Mix 1 g agarose in 99mL of TAE/TBE buffer and heat it in the oven. Add 10 uL of 10mg/mL ethidium bromide in 100 mL of hand cold agarose gel solution. Pour this mixture into gel caster/tray having comb and sealed from sides. Let it be solidified at room temperature for 30-60 minutes. Remove the comb seals from the gel caster and place it inside the gel tank containing TAE/TBE buffer. Put the DNA samples/PCR product (mixed in 6x loading dye) inside each well and note it in the lab. Notebook. Attach the cathode (towards wells) end of gel and anode (at the bottom) of the power supply to the gel tank. Switch on the power supply giving 80-120 volts and run it for sufficient time allowing the samples to travel in more than half of the gel length. Take the gel out of the gel tank and observe it in a gel doc system/UV transillumin

Total Plant RNA Isolation-Trizol Reagent Method

Total Plant RNA Isolation Using Trizol Reagent 1. Crush 100 mg of tissues in 1mL of triazole reagent by pestle mortar or micro pestle 1.5 or 2.0 mL RNase free Eppendorf tubes. *Incubate for 2-3 minutes at room temperature. 2. Add 200 uL chloroform and mix by gently inverting the tube. *Incubate for 2-3 minutes at room temperature. 3. Centrifuge at 12000xg at 4oC for 15 minutes. 4. Transfer the supernatant into fresh 1.5 mL RNA’s free tube. 5. Add 500 μL isopropanol mix gently by inverting the tube. *Incubate for 10 minutes at room temperature. 6. Centrifuge at 12000xg at 4oC for 10 minutes. *Discard the supernatant and keep the pallet in the tube. 7. Add 1mL of ice-chilled 75% ethanol to wash the pallet. 8. Centrifuge at 7500xg at 4oC for 5 minutes. *Discard the supernatant and keep the pallet in the tube. *Keep lid opened tube at 4oC for 15 min to air dry the pallet. 9. Add 50-100 uL RNA’s free water in pallet and mix by gentle pipetting. 10. Incubate for 10-15 m