There are some coating plate like Elisa. Have you heard the word "elisa" ever? It is a special kind of plate where we want to search and detect different things in liquid(endpoint binding). This plate finds huge utilization in the field of scientific research they aide identifying trace amounts of substances present in a sample. But what is an Elisa coating plate and how does it function? Come tag along and take a deep dive into this exciting tool!
Elisa coating plate, like all the other Elisa modules havethis same checkered pattern. This plastic part with lots of wells. The buckets are called wells, and each one can contain some liquid. These wells are used by scientists to trap and determine the quantities of various substances in a liquid sample. If they put a liquid into the wells, and target molecules that they're looking for is present then it would not be detected. This enables to know further on the sample they are testing.
The Elisa plate was cleaned: the necessary condition is your plate should be absolutely clean. You can clean it with soap and water rinse after using distilled waters you go on to? You must dry it with towel or machine to remove the water leftover after you wash. Even a small amount of dirt will change the final results, so this step is very critical.
Add the diluted target molecule to wells: Using a device called pipette, carefully add the diluted target molecule into those wells Exercise caution and do not touch the wells' surfaces because that might lead to contamination. And stay clear of bubbles, they can end up messing with the results as well.
Incubate the plate: Once you have added molecule of interest, then You need to allow it time in a controlled environment. This is called Incubation Period. The time and temperature for this step may vary due to the type of target molecule as well as buffer solution. Success follows the correct conditions.
Block the plate: Finally, you must prepare a solution to stop other reagents from sticking in wrong places and cover the whole research area. The blocking solution blocked out the most of plate area, where target molecule did not coat. This is a crucial step to make sure that the only molecules detected are your target.
Inadequate sticking: If you are using a target molecule that has the tendency not to bind tightly with the plate, this situation will result in insufficient coat. This can be occured by plate unpropper cleaning, mix molecule without stired. Beforehand do something about the plate, make sure to clean it so you can start pub sub shop.
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