Light cannot pass through the specimen and therefor individual cells cannot be distinguished, it just looks dark or they may look like clumps
the purpose of boiling of smear in malachite green is to forces a stain to penetrate the endospore wall, it is necessary to heat the slide and the stain to prod the wall to allow the stain to enter.
If a smear exhibits uneven thickness, overlapping cells may not get the proper exposure to the reagents. This results in uneven or mottled staining. For example, in the thicker areas of the smear, gram-negative cells may not decolorize sufficiently and end up staining purple.
The main disadvantage: it cannot be used to identify hookworm eggs. The other main argument against the Kato technique is that it is messy and therefore exposes technicians to an unnecessarily high risk of infection.Advantages of the Kato thick smear method include: it detects low infections which may be missed by the brine flotation method; it gives a higher egg count even in light infections; it is easy to prepare and this method involves less expense.
Air-drying a smear helps to fix the cells onto the slide, preventing any loss or distortion during further processing steps like staining or examination under a microscope. It also helps to evaporate any excess water, improving the visualization of the cells.
In microbiology, smear refers to the process of spreading a sample (such as bacteria or cells) onto a microscope slide for staining and observation. Smears are used to create a thin, even layer of the specimen for better visualization under the microscope.
Passing the bacterial smear through the flame before staining is done to heat-fix the bacteria onto the slide, making them adhere firmly and preventing them from washing off during the staining process. Heat fixing also kills the bacteria, which helps in the preservation of their cellular structures for visualization under the microscope.
the purpose of boiling of smear in malachite green is to forces a stain to penetrate the endospore wall, it is necessary to heat the slide and the stain to prod the wall to allow the stain to enter.
If a bacterial smear is not heat fixed prior to staining, the bacteria may not adhere well to the slide and can wash away during the staining process. Heat fixing helps to kill the bacteria, firmly attach them to the slide, and improve the uptake of stain, resulting in better staining results. Without heat fixing, the bacteria may not stain properly or may not be visible at all under the microscope.
Gram variability refers to a characteristic of certain bacteria that can exhibit variability in their response to Gram staining, appearing as a mix of both Gram-positive and Gram-negative characteristics. This variability can make the identification of these bacteria challenging because their staining characteristics may not be consistent.
If a smear exhibits uneven thickness, overlapping cells may not get the proper exposure to the reagents. This results in uneven or mottled staining. For example, in the thicker areas of the smear, gram-negative cells may not decolorize sufficiently and end up staining purple.
The main disadvantage: it cannot be used to identify hookworm eggs. The other main argument against the Kato technique is that it is messy and therefore exposes technicians to an unnecessarily high risk of infection.Advantages of the Kato thick smear method include: it detects low infections which may be missed by the brine flotation method; it gives a higher egg count even in light infections; it is easy to prepare and this method involves less expense.
It is used to fix because to make the cell inactive or immoblie, but the main purpose is to fix the smear so that when we put stain and then flush it out with water ( or some time with alcohol) the smear should not wash out with dye.
secret =p
Inoculating loops are for the transferring of microorganisms or for the staining of slides. ?æIt is also called a smear loop or a micro streaker.?æ
Air-drying a smear helps to fix the cells onto the slide, preventing any loss or distortion during further processing steps like staining or examination under a microscope. It also helps to evaporate any excess water, improving the visualization of the cells.
In microbiology, smear refers to the process of spreading a sample (such as bacteria or cells) onto a microscope slide for staining and observation. Smears are used to create a thin, even layer of the specimen for better visualization under the microscope.
because giemsa stain is a mixture of methyl acetate Eosin and azure b. it doesnot contain any fixative that is why we use methanol to fix smear during giemsa stain other stain like lieshman contain acetyl free methyl alcohol as a fixative so it does not need to fix slide stain with lieshman stain.