Which of the following is not an application of PCR (Polymerase Chain Reaction)?
Detection of gene mutation
Molecular diagnosis
Gene amplification
Purification of isolated protein
The Polymerase Chain Reaction (PCR) is a technique used in molecular biology to amplify DNA sequences. It is a fundamental method used in various applications due to its ability to amplify a small amount of DNA across several orders of magnitude, generating millions or billions of copies of a particular DNA sequence.
Let's analyze each option to see why it is or is not an application of PCR:
Conclusion: Based on the explanation above, the correct answer is Purification of isolated protein as it does not involve the application of PCR.
A constant voltage of 50 V is maintained between the points A and B of the circuit shown in the figure. The current through the branch CD of the circuit is :
The output (Y) of the given logic implementation is similar to the output of an/a …………. gate.
What is Microalbuminuria ?

In the above represented plasmid an alien piece of DNA is inserted at the EcoRI site. Which of the following strategies will be chosen to select the recombinant colonies?
DNA fingerprinting, also called DNA typing, DNA profiling, genetic fingerprinting, genotyping, or identity testing, in genetics, method of isolating and identifying variable elements within the base-pair sequence of DNA.
The procedure for creating a DNA fingerprint consists of first obtaining a sample of cells, such as skin, hair, or blood cells, which contain DNA. The DNA is extracted from the cells and purified. In Jeffreys’s original approach, which was based on restriction fragment length polymorphism (RFLP) technology, the DNA was then cut at specific points along the strand with proteins known as restriction enzymes. The enzymes produced fragments of varying lengths that were sorted by placing them on a gel and then subjecting the gel to an electric current (electrophoresis): the shorter the fragment, the more quickly it moved toward the positive pole (anode). The sorted double-stranded DNA fragments were then subjected to a blotting technique in which they were split into single strands and transferred to a nylon sheet. The fragments underwent autoradiography in which they were exposed to DNA probes—pieces of synthetic DNA that were made radioactive and that bound to the minisatellites. A piece of X-ray film was then exposed to the fragments, and a dark mark was produced at any point where a radioactive probe had become attached. The resultant pattern of marks could then be analyzed.