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What is an example of a differential medium?

An example of a differential medium is MacConkey agar, which is used to isolate and differentiate gram-negative bacteria, particularly enteric bacteria. It contains bile salts and crystal violet, which inhibit the growth of gram-positive organisms, while lactose and a pH indicator allow for the differentiation of lactose fermenters (which produce pink colonies) from non-fermenters (which remain colorless). This selective and differential property makes it useful for identifying specific bacterial groups based on their metabolic characteristics.


How many colors make the color Violet?

Violet is a secondary color. Secondary colors are achieved by mixing two of the three primary colors in equal proportions. Violet is made by mixing Blue and Red, therefore the answer is two.


What is the definition of analogous colors?

Colors that are related to each other are analogous. They are neighbors on the color wheel and share a common color. For example, blue violet, violet, and red violet. they all contain red. The Violet (a secondary color) has been made by mixing red and blue (both primary colors). The blue-violet and red-violet (both tertiary colors) have been made by mixing the secondary color (Violet) with the primary color included in it's name. They are analogous, or relatives, because they all contain red. This holds true for any three colors on the color wheel which directly in contact with each other. See the related link for more on mixing colors.


What is the genre of the song violet hour by sea wolf?

"Violet Hour" by Sea Wolf is considered to be an alternative-rock song according to iTunes.


How do you prepare 1 percent gentian violet?

1) take 10gm of gentian violet. then add to them: 2) Alcohol 70% ( H2O).... to 1000 ml

Related Questions

Could you use Congo red for positive staining or crystal violet for negative staining?

Congo red is primarily used as a negative stain, as it binds to the polysaccharides in the cell wall of certain bacteria, resulting in a red appearance against a blue background. Crystal violet, on the other hand, is commonly used for positive staining; it is the primary stain in the Gram staining procedure, where it stains the peptidoglycan layer of Gram-positive bacteria, turning them purple. Thus, Congo red is not suitable for positive staining, while crystal violet is not typically used for negative staining.


What is the function of crystal violet in the gram staining process?

Crystal violet is used in the Gram staining process to initially stain all bacteria purple. This helps differentiate between Gram-positive and Gram-negative bacteria based on their ability to retain or lose the crystal violet dye during the staining process.


Is the crystal violet test result positive or negative?

The crystal violet test result is positive.


Is anthrax gram positive or negative?

Anthrax is a gram-positive bacterium, meaning it retains the crystal violet stain in the Gram staining procedure.


What is the purpose of crystal violet in the process of gram staining?

Crystal violet is used in the process of gram staining to initially stain all bacteria purple. This helps differentiate between gram-positive and gram-negative bacteria based on their cell wall composition.


What is the role of crystal violet in the process of gram staining?

Crystal violet is a purple dye used in the gram staining process to initially stain all bacteria cells. It helps differentiate between gram-positive and gram-negative bacteria based on their cell wall composition.


Why is Iodine used in Gram staining?

Iodine is used in Gram staining as a mordant, which helps to bind the crystal violet dye to the cell wall of bacteria. This mordant-iodine complex forms larger complexes with the crystal violet dye, making it difficult for the dye to be washed away during the decolorization step. This allows for differentiation of Gram-positive and Gram-negative bacteria based on their ability to retain the crystal violet dye.


Explain why crystal violet would not be useful in the negative stain technique?

Negative staining techniques are designed to stain everything BUT the bacterial cells. This allows us to see the cells unstained and helps us observe their morphology (how the cells are shaped and how they group together). The cells have an overall negative charge on their surface, so they naturally attract positive charges. Crystal Violet carries a positive charge, so it would adhere to the surfaces of the cells thus staining the cells (which is not what you want in a negative stain!)


Function of Gram's iodine?

Iodine is used as a mordant in the gram staining procedure to make large crystals when it is used with crystal violet dye. In gram positive cell walls those crystals get stuck and wont get washed off with the alcohol. In gram negative cell walls the crystals are washed out.


What is the most important reagent in gram staining the least important?

In gram staining, the most important reagent is crystal violet, which is the primary stain that colors all bacteria. The least important reagent is safranin, the counterstain, which provides contrast by staining gram-negative bacteria after the decolorization step. While both are essential for the procedure, crystal violet is critical for differentiation between gram-positive and gram-negative bacteria.


What are the functionally analogous pair of stains?

Crystal violet and safranin are functionally analogous pair of stains in the Gram staining technique. Crystal violet stains gram-positive bacteria purple/blue, while safranin counterstains gram-negative bacteria pink/red.


Why is timing so critical when decolourizing in Gram staining?

Timing is critical when decolorizing in Gram staining because if the decolorizer is left on for too long, it can wash away the crystal violet stain from Gram-positive cells, leading to a false negative result. Conversely, if the decolorizer is not left on long enough, the crystal violet stain may not be fully removed from Gram-negative cells, leading to a false positive result. Timing ensures accurate differentiation between Gram-positive and Gram-negative bacteria.