Answer:
The result will give a smear background of red color or pink , while the specimen(cell) will turn blue.This is an example of ROMANOWSKY staining.Its main objective is to increase the contrasts for better view.
Explanation:
Histologically, staining is the process of adding colors to the speciemen under focus who can not be discern with naked here to have increase in contrast to ensure a well defined view.
Eosin is a staining dye that is acidic in nature, while methylene blue is basic,the reaction mixture will separate the red color background of from the blue color of the cell giving a clear contrast .
This technique is mainly used for
1. blood staining and bone marrow staining (biopses) for disease detection.
2.malaria detection.
3. for Cerecrospinal fluid and lumber puncture staining,in cytopathology.
<u>Eviences has shown that;the mixture of eosin and methylene blue do not produce the red/blu coloration, but rather the replacement of the methylene blue with AZURE B</u>
malaria detection
The appropriate response is compost piles. It is a heap of substituting layers of plant garbage and soil regularly with an admixture of creature excrement or compound manure masterminded so a to energize the quick change of the constituents into fertilizer.
The first day of last menstrual cycle.
To identify, map, and evaluate the underlying biochemical processes of cell signaling, it is essential to visualize cells and cellular structures as well as track and modify nucleic acids and proteins in living cells.
<h3>How cell labeling of mammalian cells done?</h3>
- Mammalian cells can be magnetically labeled by combining ferumoxides or superparamagnetic iron oxide (SPIO) with transfection agents (TAs).
- The effectiveness and survivability of cell labeling with TAs complexed to SPIO have not been systematically compared. This study examines the toxicity and labeling effectiveness of FEs complexed to various TAs in mammalian cells at various doses.
- TAs from several classes, including lipid-based substances, dendrimers, and polycationic amines, were employed.
- TAs at concentrations ranging from 1 to 50 microg/mL in incubation media were used to measure the cellular toxicity. Combining varying doses of TAs with various amounts of FEs allowed researchers to calculate the iron incorporation efficiency.
Learn more about the cell labeling with the help of the given link:
brainly.com/question/16758407
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