03/02/2022
When it comes to starting to use a new reagent in the lab, what is the correct way to do it? 🤓
➡️The main rule is as follows: before you start actively using a new reagent in your work, you need to test it directly in your laboratory. Of course, in production, the reagent has passed quality control, it has an instruction where all important indicators are described, BUT you need to understand how this or that substance works directly in your conditions. Because, yes, each laboratory is unique. :)
➡️Validate not on diagnostic material, but on test material! Act according to the scheme (we will demonstrate this using formalin as an example):
✳️During the grossing from the organ, additionally take several pieces which have no diagnostic value, and then you will conduct a check test on them.
✳️Fix diagnostically significant pieces into “old” formalin, while those pieces additionally grossed - into the “new”.
✳️At all other stages of the histoprocess, work with “old” and “new” pieces in the same way, according to the protocols established in the laboratory. The idea is that in order to test something, you only have to change one stage.
✳️At the output, check the difference in the result.
If the quality of the slide has not suffered with the introduction of a new reagent, you can safely introduce it into your work.