Course Content
Microscopes and Microscopy
MICROSCOPES AND MICROSCOPY OBJECTIVES By the end of this topic, the trainee should be able to: 1.Name various types of microscopes. 2.State the function of parts of a microscope. 3.Describe the use of compound light microscopes describe care and maintenance of compound microscopes. 4.Describe preparation of microscope slides
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The Cell
OBJECTIVES By the end of this topic, the trainee should be able to: 1.Define and explain meaning of terms. 2.State types of cells. 3.Describe the cell structure under the light microscope. 4.State the functions of cell organelles. 5.Describe the process of mitosis and meiosis. 6.Describe physiological processes of cells. 7.describe the techniques of cell isolation. 8.Describe the procedure of temporary cell preparation.
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Microorganisms
OBJECTIVES By the end of this topic , the trainee should be able to: 1.Classify the major groups of microorganisms. 2.State the general characteristics of each group. 3.Explain their mode of nutrition and reproduction. 4.Describe culture media. 5.Describe culturing techniques for bacteria. 6.Describe methods for determining bacteria population. 7.Describe sterilization and disinfection techniques.
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Immunological Techniques
OBJECTIVES By the end of this topic, the trainee should be able to: 1.Define terms. 2.Describe types of immunity. 3.Describe types of immune cells. 4.Describe the lymphoid organs and tissues. 5.Describe serological and immunological techniques.
0/8
Herbarium Techniques
OBJECTIVES By the end of this topic , the trainee should be able to: 1.Explain terms 2.Describe importance of collecting and preserving herbarium specimens 3.Describe sources of herbarium specimens 4.Describe collection of herbarium specimens 5.Describe preservation of herbarium specimens 6.Describe display of herbarium specimens
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Museum Techniques
OBJECTIVES By the end of this topic, the trainee should be able to: 1.Explain terms. 2.Describe importance of collecting and preserving museum specimens. 3.Describe sources of museum specimens. 4.Describe collection of museum specimens. 5.Describe preservation of museum specimens. 6.Describe display of museum specimens
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Vivarium Techniques
OBJECTIVES By the end of this topic, the trainee should be able to: 1.Explain terms. 2.Describe importance of vivarium. 3.Describe essential features of a vivarium. 4.Describe construction of a vivarium. 5.Describe maintenance of a vivarium.
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Aquarium Techniques
OBJECTIVES By the end of this topic, the trainee should be able to: 1.Explain terms. 2.Describe importance of aquariums. 3.Describe essential features of an aquarium tank. 4.Describe construction of an aquarium tank. 5.Describe maintenance of an aquarium tank.
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Laboratory Animals
OBJECTIVES The objective of this chapter is to give a better understanding of the technical requirements regarding handling, care and maintained of various laboratory animals In this chapter, we will; 1. Identify the various types of laboratory animals. 2.Discuss the general care and handling of laboratory animals. 3. Describe the various methods of restraining and humane killing laboratory animals 4.Discuss care of specific disease free (SPF)and Gnotobiotic animals
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Introduction to Ecology
OBJECTIVE By the end of this module, the trainee should be able to: 1.Explain terms. 2.Describe biotic and abiotic factors. 3.Explain adaptation of organisms to terrestrial and aquatic environment. 4.Describe the energy flow in ecosystem. 5.Explain estimation of population in ecosystem. 6.Describe influence of human activities on environment. 7.Describe basic biogeochemical cycles.
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Plant Anatomy and Physiology
OBJECTIVES By the end of this topic, the trainee should be able to: 1.Describe of plant parts and tissues. 2.Describe functions of various plant tissues. 3.Describe processes in plants .
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Biology Techniques For Science Laboratory Technicians
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Culture Media

Culture media, also known as growth media or nutrient media, are specially formulated substances used to support the growth, proliferation, and study of microorganisms (such as bacteria, fungi, and viruses) and cells in a laboratory setting. These media provide essential nutrients, energy sources, and other growth-promoting factors necessary for the organisms to grow and survive. Culture media can be categorized into two main types:

  1. Solid Media: Solid media are used to grow microorganisms and cells as colonies or discrete units. They typically contain solidifying agents, such as agar, which solidifies the media while remaining inert to most microorganisms. Solid media allow for the isolation and identification of individual colonies and are commonly used for streaking, isolating pure cultures, and performing various microbiological tests. Examples of solid media include nutrient agar, MacConkey agar, and blood agar.

  2. Liquid Media: Liquid media are used when a larger quantity of microorganisms or cells is needed or when the growth characteristics of the organism are being studied. Liquid media are usually in a broth form and are commonly used for the propagation of cultures, performing growth experiments, and conducting biochemical tests. They are often used in shake flasks, bioreactors, or other containers with adequate aeration and mixing. Examples of liquid media include nutrient broth, tryptic soy broth, and Sabouraud broth for fungal cultures.

Culture media can be classified into various types based on their composition, purpose, and specific applications. Here are some common types of culture media:

  1. Complex Media: Complex media are nutrient-rich media that contain various complex components of unknown chemical composition, such as beef extract, peptone, or yeast extract. These media can support the growth of a wide range of microorganisms by providing a diverse array of nutrients.
  • Defined Media: Defined media have a precisely known composition, with individual components and their concentrations specified. These media are often used for studying specific metabolic pathways, nutritional requirements, or for the growth of organisms with specific nutritional needs.

  • Selective Media: Selective media contain specific components that selectively inhibit the growth of certain microorganisms while allowing the growth of desired organisms. These media are commonly used for the isolation and identification of specific bacterial or fungal species from mixed cultures. Examples include MacConkey agar (selective for gram-negative bacteria) and Sabouraud dextrose agar (selective for fungi).

  • Differential Media: Differential media contain specific components that allow the differentiation of different types of microorganisms based on their metabolic or biochemical characteristics. These media often include indicators such as dyes or pH indicators that produce visible color changes or other observable reactions. Examples include blood agar (used to differentiate hemolytic bacteria) and mannitol salt agar (used to differentiate staphylococci based on their ability to ferment mannitol).

  • Enriched Media: Enriched media are formulated to provide additional nutrients that support the growth of fastidious microorganisms, which have specific nutritional requirements. They contain extra growth factors, such as blood components, serum, or special additives, to enhance the growth of these organisms. Examples include blood agar, chocolate agar, and Thayer-Martin agar.

  • Enrichment Media: Enrichment media are designed to selectively enrich the growth of certain microorganisms by providing specific growth factors or nutrients that are lacking in other media. These media are commonly used when the target organism is present in low numbers or is difficult to isolate. Examples include Selenite broth (used for the enrichment of Salmonella) and Thayer-Martin agar (used for the enrichment of Neisseria gonorrhoeae).

  • Basal Media: Basal media are the basic or general-purpose media that provide essential nutrients for the growth of a wide range of microorganisms. They contain a mixture of organic and inorganic compounds, vitamins, and energy sources. Examples include nutrient agar and nutrient broth.

  • Transport Media: Transport media are used to maintain the viability and prevent the overgrowth or death of microorganisms during transportation from one location to another. They often contain buffering agents to maintain pH, antimicrobial agents to inhibit bacterial growth, and cryoprotectants for the preservation of samples. Examples include Stuart’s transport medium and Amies transport medium.

  • Synthetic or Defined Media: Synthetic or defined media have precisely known compositions with individual components and their specific concentrations specified. They are often used for studying the specific nutritional requirements, metabolic pathways, or growth characteristics of microorganisms. Synthetic media allow for precise control and reproducibility of experimental conditions.

  • Anaerobic Media: Anaerobic media are used for the cultivation of anaerobic microorganisms that require oxygen-free conditions for growth. These media are typically prepared in oxygen-free environments and may contain reducing agents to remove oxygen and create anaerobic conditions.

  • Specialized Media: Specialized media are designed for the growth of specific types of microorganisms or for specific purposes. Examples include Sabouraud agar for fungal cultures, Lowenstein-Jensen medium for Mycobacterium tuberculosis, and Luria-Bertani (LB) broth for the growth of Escherichia coli.

The choice of culture media depends on the specific requirements of the microorganism or cells being cultured, the purpose of the study, and the desired outcomes. It is important to select the appropriate media to ensure optimal growth, viability, and the ability to obtain accurate results for the intended applications.

The selection of the appropriate culture media depends on the type of microorganism or cells being cultured, the specific requirements of the experiment or study, and the goals of the researcher.

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