Step 1: Understanding the Methods
- ELISA: A technique used for detecting and quantifying soluble substances like proteins or antibodies, not suitable for detecting nucleotide changes.
- WESTERN Blotting: Used for detecting proteins, not nucleotides.
- SDS-PAGE: A technique for protein separation, not used for detecting DNA sequence changes.
- PCR: Correct, PCR can be used to detect single nucleotide changes by amplifying specific DNA regions and comparing the sequences.
Step 2: Conclusion
PCR is the most suitable method for detecting single nucleotide changes in DNA.
A closed-loop system has the characteristic equation given by: $ s^3 + k s^2 + (k+2) s + 3 = 0 $.
For the system to be stable, the value of $ k $ is:
A digital filter with impulse response $ h[n] = 2^n u[n] $ will have a transfer function with a region of convergence.