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New York City Agar Composition, Preparation, Result, Uses

New York City Agar Composition, Preparation, Result, Uses

NYC Agar Base medium was initially created by Fauer, Weisburd and Wilson at the New York City Department of Health to isolate the pathogenic Neisseria strains from human samples. NYC medium, designed primarily to isolate pathogenic Neisseria is also able to support the growth of mycoplasmas with large colonies or mycoplasmas T (Ureaplasma). It is a translucent medium, highly selective, allowing direct microscopic observations and presumed identification of mycoplasmas and Neisseria gonorrhoeae.

Alkaline Phosphatase Test of Milk- Determination of Phosphatase Activity of Milk

Alkaline Phosphatase Test of Milk- Determination of Phosphatase Activity of Milk

Alkaline Phosphatase (ALP) is an enzyme that is naturally found within all the raw milks that is utilized to determine the quality of pasteurization of milk. A complete pasteurization process can deactivate the enzyme below levels that can be detected by traditional methods. Because the stability of the heat of ALP is higher than the stability of pathogens that could be found in milk, it serves as a metric of security. However, failure for detection of ALP activity is not a mean an item is safe from pathogens.

Mannitol Salt Agar (MSA) Composition, Principle, Preparation, Results, Uses

Mannitol Salt Agar (MSA)

Mannitol Salt Agar (MSA) is utilized as a differential and selective medium to isolate and detect Staphylococcus aureus in clinical and non-clinical samples. It is recommended for identification and enumeration of coagulase positive Staphylococci that are present in milk, food as well as other specimens. MSA also promotes an increase in the number of particular group of specific bacteria, while limiting the growth of other bacteria.

Xylose Lysine Deoxycholate (XLD) Agar Composition, Preparation, Principle, Uses

Xylose Lysine Deoxycholate (XLD) Agar Composition, Preparation, Principle, Uses

Xylose Lysine Deoxycholate agar (XLD) is a selective medium that allows for the isolation and growth of Salmonella and Shigella species using clinical samples or food. Taylor developed XLD Agar to aid in the differentiation, isolation and identification of enteric disease agents and support the growth more specialized enteric organisms. XLD Agar is a well-proven medium that allows the growth of Shigella species. It is also an excellent medium to isolate Salmonella species. It has a pH value of 7.4, giving it a bright pink to red color due to the indicator phenol. 

Types of Blood Collection Tubes and Their uses

Types of Blood Collection Tubes and Their uses

Evacuated Tubes that are used for blood collection for different laboratory tests are made up of tubes in variable sizes, and color-coded tops to indicate tube contents. The majority of blood collection tubes contain an ingredient that either speeds up the blood’s clotting (clot activator) or stops blood from becoming clot-free (anticoagulant). The following list lists the most frequently utilized blood collection tubes, along with their additives, and their uses in lab:

Nagler Reaction – Lecithinase Test

Nagler Reaction - Lecithinase Test

Nagler’s Reaction or Lecithinase test is a test in biochemistry used to detect organisms that produce the phospholipases (lecithinases) e.g. Clostridium perfringens. Its alpha (a) toxin from C. perfringens exhibits the phospholipase enzyme activity, which aids in the distinction between C. perfringens and the other Clostridium species that generate the enzyme lecithinase (C.baratti, C.absonum, C.bifermantans, C.sordelli, and C.novyi) through neutralization of lecithin C activity with an antitoxin.

Moist Heat Sterilization Principle, Advantages, Disadvantages

Moist Heat Sterilization Principle, Advantages, Disadvantages

Of all the options to sterilize (killing or eliminating all microorganisms, which includes the spores of bacterial growth) moist heat that is saturated steam with pressure has been the most frequently utilized and most reliable method. Moisture has more penetrating power than dry heat, and at a certain temperature, causes a greater reduction in the quantity of live microorganisms. Steam sterilization is safe cheap, low-cost, quickly microbicidal, as well as sporicidal. It quickly heats and penetrates into fabrics.

Albert Stain Principle, Procedure, Result

Albert stain Principle, Procedure, Result

Different stains have been developed over time to distinguish bacteria species, separating them morphologically and the specific characteristics they possess. The most popular stain is Gram staining, acid-fast staining, and endospore staining. Each stain aims at identifying and defining bacteria according to their forms and morphologies.

Types of Stains used in Microbiology

Types of Stains used in Microbiology

Different stains react or concentrate on different areas of a tissue or cell These properties can be utilized to highlight certain areas or regions. A few of the most well-known biological staining methods can be found below. If not otherwise indicated All of these dyes can be used on tissues and cells that are fixed as well as essential dyes (suitable for use in live organisms) are indicated.

McIntosh and Fildes’ Anaerobic Jar Principle, Procedure

McIntosh and Fildes’ Anaerobic Jar Principle, Procedure

McIntosh and Fildes’s anaerobic jar is a tool utilized in microbiology laboratories, to generate anaerobic circumstances (anaerobiosis) to cultivate obligate anaerobes, such as Clostridium spp. Anaerobiosis derived from McIntosh and Fildes anaerobic jar is among the most effective and most frequently employed methods for anaerobiosis however it requires expensive special equipment and a vacuum pump. Gas supply availability is another drawback to this technique. It is currently being replaced with an easier GasPak system.

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