On the last day, we worked on ELISA testing or Enzyme Linked
Immune Sorbent Essay. This test is used to detect the presents of antibodies.
When you get sick, your body will produce antibodies for the antigens present in
the disease. Being able to detect these antibodies is useful; as in AIDS, the
virus hides where it cannot be detected inside our cells. However, the
antibodies are not hiding so they can be detected.
Materials:
- ELISA kit
- piquet
- buffer
- 12-well micro plate strip
- paper towels
Procedure:
First, we labeled the wells. The first 3 are going to be a positive control test, the
next 3 are negative control test, the next three were sample 8, and the last 3
were sample 38.
We add 50µl of the antigen and let it sit for 5 minutes then
wash. To wash we tip the wells over on the paper towels and gently tapped, then
filled the wells with the buffer and again tipped them over and tapped out the
liquid on fresh paper towels. After that we added the positive control, the
negative control, serum 8, and serum 38 to the appropriate wells, waited 5
minutes and washed. Repeating the same
motion we added the secondary antibody, waited and washed. The final step was
to add the enzyme substrate.
Results/applications:
The first 2 wells and the last 3 wells turned blue
right away. So one of our positive controls was not done correctly as the 3rd
well should have also turned blue. These results would also indicate that the
serum 38 is positive for antibodies and serum 8 is negative.
This test also showed us how quick and simple it is to test
for antibodies to detect diseases that are able to hide in our own cells in our
body.
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