8
lol, we must be in the same class, b/c i have all of the same questions. did u figure out the answer? I think its a base ... qc the microbiology lab Cute, from the best that I could find some sources say pH 7 and others had given a pH 8. But could not find a solid answer. As a simple stain it would have to have a pH of <7. As we know, the charge on the cell is always going to be negative (an anion). In order to achieve a simple stain we want the stain attracted to the cell wall; therefore, the stain must be positively charged (a cation) for the opposite forces to attract. The more acidic the compound - the smaller its pH number with 7 being neutral. As we know, the [H]+ increases as the pH decreases becoming evermore positively charged. Simple answer: <7
This compound is basic.
The counter stain used in the Gram stain procedure is typically safranin or basic fuchsin, which stains Gram-negative bacteria pink or red. In the acid-fast stain procedure, the counter stain used is typically methylene blue or brilliant green, which stains non-acid-fast bacteria blue or green, allowing acid-fast bacteria to retain the primary stain color (carbolfuchsin).
Negative stain is used in electron microscopy to visualize the outer surface of specimens, as the stain does not penetrate the sample. It is particularly useful for observing the morphology and arrangement of bacterial cells and flagella.
Both processes use 2 stains. The Gram staining process uses crystal violet as the primary stain and safranin as the secondary stain. Acid-fast staining uses carbol fuchsin as the primary and methylene blue as the secondary.
lol, we must be in the same class, b/c i have all of the same questions. did u figure out the answer? I think its a base ... qc the microbiology lab Cute, from the best that I could find some sources say pH 7 and others had given a pH 8. But could not find a solid answer. As a simple stain it would have to have a pH of <7. As we know, the charge on the cell is always going to be negative (an anion). In order to achieve a simple stain we want the stain attracted to the cell wall; therefore, the stain must be positively charged (a cation) for the opposite forces to attract. The more acidic the compound - the smaller its pH number with 7 being neutral. As we know, the [H]+ increases as the pH decreases becoming evermore positively charged. Simple answer: <7
Carbolfuchsin can be used as a counterstain in certain staining techniques, particularly in the acid-fast staining method used to detect acid-fast bacteria like Mycobacterium tuberculosis. It helps to differentiate acid-fast bacteria, which retain the primary stain (carbolfuchsin), from non-acid-fast bacteria which are counterstained with a contrasting color.
This compound is basic.
The counter stain used in the Gram stain procedure is typically safranin or basic fuchsin, which stains Gram-negative bacteria pink or red. In the acid-fast stain procedure, the counter stain used is typically methylene blue or brilliant green, which stains non-acid-fast bacteria blue or green, allowing acid-fast bacteria to retain the primary stain color (carbolfuchsin).
Since there is no heat fixing or strong cemicals are used the bacteria are less distorted
Negative stain is used in electron microscopy to visualize the outer surface of specimens, as the stain does not penetrate the sample. It is particularly useful for observing the morphology and arrangement of bacterial cells and flagella.
Negative staining has a dark contrasted background and the bacteria is white. Simple staining has a white background and bacteria is the color depended on your stain color.Negative staining when prepared is NOT heat fixed but simple staining when prepared is heat fixed. Heat fixed means when preparing slide with bacteria on it, it is passed over some type of flame, like a Bunsen burner flame, three times or four times.
Both processes use 2 stains. The Gram staining process uses crystal violet as the primary stain and safranin as the secondary stain. Acid-fast staining uses carbol fuchsin as the primary and methylene blue as the secondary.
Yes, uranyl acetate is used as a negative stain in electron microscopy.
Methylene blue
Pink Dye
B. subtilis is indeed a Gram positive rod.However, there is confusion as to whether it is an obligate aerobe or a facultative anaerobe. Although classed as an obligate aerobe, it has been shown to grow under strict anaerobic conditions.