Linear Observation

339 Words1 Page

Two Observations (Buffy Coat Layer and Wright Stain Slide):
The buffy coat layer is the layer where the lymphocytes are located after being added with Ficoll-Paque and centrifuged. It was light colored, milk-y looking, and not very thick. It was tricky to separate that layer from the rest of the blood components using a pipette because it was such a small layer.
The Wright stained lymphocytes were dark pink and pale pink in color. The size of the cells varied, some were quite large, and others were smaller. Some were clumped together in "swirls" and "lines" of cells, while other areas of the slide looked like a polka dot pattern.

P-Value:
The results did not support hypothesis that there would be more stained cells than unstained cells. In every individual sample, more than half of the cells counted were unstained, living cells. The P-Value calculated from the data table was 0.128, therefore we fail to reject the null hypothesis. For our own individual data, this is especially true with a % viability of 98.8%. …show more content…

The average percentage of T-Cells found in the lymphocytes of human blood is about 7% - 24% (STEMCELL 2017). Three of the seven groups had %T-Cell values within this range.
Despite the whole blood sample that was used for this experiment being delivered many days before being used, the viability of the lymphocytes was still very high for most of the group data. This data could be inaccurate due to the device used to count the cell viability, the hemocytometer, because subjectivity of the individuals counting the cells or misuse of the technology itself (Cell Counting 2018). Possible errors that could have led to a lower percent viability could be not pipetting the leukocytes gently enough, causing them to

More about Linear Observation

Open Document