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It is used in gram staining to differentiate gram negative and gram positive bacteria. After being dyed, the cells are washed with ethanol. Gram positive bacteria will retain the methylene blue due to the amount of peptidoglycan in their cell walls, where gram negative cells will not. Iodine is used as a counter stain, which is up-taken by gram negative cells.

After the gram staining procedure is finished, gram positive cells will appear dark purple or blue due to the retained methylene blue. Gram negative cells will appear pink or red due to the iodine counter stain.

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Why cant methylene blue be used in place of nigrosin in negative staining?

Because negative staining requires the use of an acidic stain, which will not penetrate the cells because of the negative charge on the surface of the bacteria. As a result, the unstained cells can be easily identified against the colored background.


Is it useful to stain the Elodea and Anabaena cells with methylene blue stain?

Staining Elodea and Anabaena cells with methylene blue can be useful in microscopy to enhance contrast and visualize cell structures more clearly. Methylene blue is commonly used as a general stain to highlight cellular components such as nuclei and cytoplasm. This staining technique can aid in identifying cellular organelles and structures during microscopic examination.


What bacterial staining technique is it when a basic dye is utilized to stain bacterial cells?

The bacterial staining technique where a basic dye is used to stain bacterial cells is called simple staining. In this technique, the positively charged dye binds to the negatively charged bacterial cell structures, making them more visible under a microscope.


What can be used for a simple stain procedure?

Perhaps Gram Staining? Steps are as follows: 1. Crystal Violet, 2. Iodine, 3. Decolorizer, 4. Safrinin


Is endospore staining differencial staining?

Yes, endospore staining is a type of differential staining. It is used to distinguish between bacterial endospores and the vegetative cells of the organism. The endospores appear as green structures against a pink or red background when using the Schaeffer-Fulton staining technique.

Related Questions

What is thee purpose of adding methylene blue to the specimen?

Adding methylene blue to a slide will stain animal cells and make the nuclei more visible.


When a fixed smear of bacterial cells come in contact with methylene blue and all cells appear blue under the oil lens this is an example of?

When a fixed smear of bacterial cells comes into contact with methylene blue and all cells appear blue under the oil lens, this is an example of a basic staining technique. Methylene blue is a cationic dye that binds to the negatively charged components of bacterial cells, allowing for visualization. This staining method helps to highlight the morphology and arrangement of the bacteria, making them easier to observe under a microscope.


Staining preparation with eosin and methylene blue?

Eosin is a red stand and methylene blue is blue. The result of staining a bacterial smear with a mixture of eosin and methylene blue is that eosin is acidic and acts as a negative stain. Methylene blue is basic the smear background would turn out red while the cells would turn out blue.


Can food coloring be used to substitute methylene blue in staining cheek cells?

iodine


Methylene blue can be prepared as a basic stain or an acidic stain. How would the pH affect the staining of bacteria?

When methylene blue is prepared as a basic stain, it will have a positive charge and selectively bind to negatively charged components of bacterial cells, such as nucleic acids, enhancing the staining of bacteria. On the other hand, if prepared as an acidic stain, it will have a negative charge and repel bacterial cells, resulting in poor staining of bacteria.


Why safranine and not methylene blue is used to stain plant cells?

Both are used in staining but for different purposes .


What is the substance that have the same function as methylene blue?

One substance that has a similar function as methylene blue is crystal violet. It is commonly used in staining techniques for microbiological studies and exhibits similar properties in terms of staining cells and tissues.


When is heat fixing appropriate to a negative stain on a bacterial sample?

Heat fixing is generally not appropriate for negative staining because it can alter the shape and size of the bacterial cells, leading to inaccurate results. Negative staining relies on the use of acidic dyes that do not penetrate the cells, allowing for clear visualization of the cell's morphology and size against a contrasting background. Heat fixing can cause cells to shrink or distort, which defeats the purpose of using a negative stain. Therefore, it is best to avoid heat fixing when preparing samples for negative staining.


Why cant methylene blue be used in place of nigrosin in negative staining?

Because negative staining requires the use of an acidic stain, which will not penetrate the cells because of the negative charge on the surface of the bacteria. As a result, the unstained cells can be easily identified against the colored background.


What is the stain blue used to stain animal cells?

Methylene blue is used for many different staining purposes, but one of the main ones is staining RNA or DNA. In animal cells, it will stain the cytoplasm and the nucleus (the nucleus will be much darker).


Is it useful to stain the Elodea and Anabaena cells with methylene blue stain?

Staining Elodea and Anabaena cells with methylene blue can be useful in microscopy to enhance contrast and visualize cell structures more clearly. Methylene blue is commonly used as a general stain to highlight cellular components such as nuclei and cytoplasm. This staining technique can aid in identifying cellular organelles and structures during microscopic examination.


What bacterial staining technique is it when a basic dye is utilized to stain bacterial cells?

The bacterial staining technique where a basic dye is used to stain bacterial cells is called simple staining. In this technique, the positively charged dye binds to the negatively charged bacterial cell structures, making them more visible under a microscope.