To use the p-anisaldehyde stain in histological analysis, first prepare a solution of p-anisaldehyde in glacial acetic acid. Then, apply the stain to the tissue sample on a microscope slide and allow it to react for a specific amount of time. Rinse the slide with alcohol and water to remove excess stain. Finally, examine the stained tissue under a microscope to observe any specific structures or features.
To remove a stain using Surf powder detergent, first wet the stained area with water. Then, apply a small amount of Surf powder detergent directly to the stain and gently rub it in. Let it sit for a few minutes before washing the item as usual. The detergent should help break down the stain and lift it from the fabric.
The most critical step of gram staining is the decolorization step as crystal violet stain will be removed from both G+ve & G-ve cells if the decolorizing agent(e.g alchohol ) is left on too long.
From what i read in my book: Because the capsule is nonionic, unlike the bacterial cell, the primary stain adheres to the capsule without binding to it. Since the capsule is water- soulube, copper sulfate, rather than water, is used to wash the purple primary stain out of the capsular material without removing the stain that is bound to the cell wall.
Sodium bicarbonate is used to adjust the pH of the staining solution in the Gram stain procedure. Merthiolate is used as a mordant to enhance the crystal violet staining in the Gram stain. Together, they help differentiate between Gram-positive and Gram-negative bacteria based on their cell wall characteristics.
Lithium carbonate is used in Hematoxylin and Eosin (H&E) staining as a mordant, which helps to intensify the staining of cell nuclei with hematoxylin. It aids in achieving better contrast and clearer differentiation between cell structures in histological samples.
The Schmorl's stain procedure makes use of pararosaniline as one of its staining components. It is a histological staining method used to highlight cellular structures in tissues.
Giemsa stain is a histological stain commonly used in cytogenetics to visualize chromosomes. It stains the DNA in the chromosomes, highlighting their structural features and allowing for the analysis of chromosomal abnormalities. Giemsa stain is also used in microbiology to differentiate between different types of bacteria based on their staining properties.
The counter or secondary stain used in the Gram stain procedure is safranin.
Maneval's stain is a histological stain used for the detection of glycogen in tissues. It involves the use of periodic acid to oxidize the glycogen followed by Schiff's reagent to stain the oxidized glycogen magenta. Manaval's stain is commonly used in the study of liver and muscle tissues.
Its the primary stain of the procedure. IT stains the Gram positive organisms
A gram stain procedure typically takes about 10-15 minutes to complete.
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).
Hematoxylin and eosin (H&E) stain is commonly used for histological analysis of whole eyeballs. This stain allows visualization of the various structural components of the eye, including the cornea, iris, lens, retina, and optic nerve. Other stains, such as periodic acid-Schiff (PAS) or Masson's trichrome, can also be used for specific structures or pathological conditions in the eye.
A chemical used to stain tissue samples for laboratory analysis.
Enterobacter cloacae is a Gram-negative bacterium. It will stain pink or red in a Gram stain procedure.
No. safranin is the classic stain used in gram staining. Concentrated Carbol Fushin is mainly used for the ZN staining procedure to stain organisms such as Vibrio cholerae and Cryptosporidium. Diluted Carbol Fushin can however be used as a replacement counterstain for Safranin in the gram stain.
Capsules appear as a clear halo surrounding stained bacteria when using the capsule stain procedure. The capsule itself does not stain, allowing it to show up as a clear area against the stained background of the bacteria.