A series of cell culture samples, each expected to have different Ca^+2 expressi
ID: 3439896 • Letter: A
Question
A series of cell culture samples, each expected to have different Ca^+2 expression levels due to their different states of hypoxia, were analyzed using two different techniques; fluorescence ativated cell sorting (FACS) and fluorescence resonance energy transfer (FRET). The results of the Ca^+2 expression levels from the FACS analyses provided values of
Sample 1= 3.2 mM
Sample 2= 12.8 mM
Sample 3= 7.3 mM
Sample 4= 1.0 mM
Sample 5= 5.4 mM
Sample 6= 6.1 mM
Sample 7= 2.2 mM
The results from the FRET analyses for the exact same 7 samples revealed values of;
Sample 1= 2.8 mM
Sample 2= 12.6 mM
Sample 3= 7.7 mM
Sample 4= 1.2 mM
Sample 5= 5.5 mM
Sample 6= 5.6 mM
Sample 7= 2.7 mM
Based on these results , is the accuracy of the FRET analysis method the same as that of the FACS analysis method at the 95% confidence level? (Show calculation)
Explanation / Answer
Ho : Mean (FACS) = Mean (FRET)
Ha : Both the means are different
We carry out t-stat test. The calculation is shown in the tabular format
Since the two tailed critical value (2.4469) is greater than calculated t-stat ( -0.0971), the null hypothesis can't be rejected.
Thus, we can say that the two tests give the same results.
Hope this helps. Ask if you don't understand anything.
Sample FACS FRET 1 3.2 2.8 2 12.8 12.6 3 7.3 7.7 4 1 1.2 5 5.4 5.5 6 6.1 5.6 7 2.2 2.7 t-Test: Paired Two Sample for Means FACS FRET Mean 5.429 5.443 Variance 15.549 14.810 Observations 7 7 Pearson Correlation 0.995 Hypothesized Mean Difference 0 df 6 t Stat -0.0971 P(T<=t) one-tail 0.4629 t Critical one-tail 1.9432 P(T<=t) two-tail 0.9258 t Critical two-tail 2.4469Related Questions
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