Given below are two sets of terms related to various methods used in biological science. Which one of the following options correctly matches terms of Column A and Column B?Column A Column B A. RACE (i) DNA-protein interactions B. South-Western blotting (ii) FAM C. Recursive PCR (iii) Determining
the ends of mRNAD. TaqMan (iv) Construction
of synthetic DNA
The question asks us to match different biological techniques listed in Column A with their specific applications or associated terms listed in Column B. Let's analyze each term in Column A and find its correct match in Column B.
Based on the analysis above, we can establish the following matches:
Let's represent this matching in a table format for clarity.
| Column A (Method) | Column B (Application/Term) | Match |
|---|---|---|
| A. RACE | (iii) Determining the ends of mRNA | A - (iii) |
| B. South-Western blotting | (i) DNA-protein interactions | B - (i) |
| C. Recursive PCR | (iv) Construction of synthetic DNA | C - (iv) |
| D. TaqMan | (ii) FAM | D - (ii) |
The correct combination of matches is A - (iii), B - (i), C - (iv), and D - (ii).
Which one of the following does NOT use RNA-sequencing?
Which one of the following statements related to molecular cloning procedures is INCORRECT?
Amongst the following, which one is the most appropriate strategy to sequence and assemble highly repeated regions of a genome?
Given below are statements related to various molecular techniques
A. During molecular cloning of DNA fragments, a vector and insert molecule digested with two different enzymes can never be ligated with each other.
B. Only 3' → 5' exonucleases and not 5' → 3' exonucleases can be used for digesting nucleic acids to generate blunt-ended fragments for cloning.
C. In Sanger's dideoxy sequencing method, each reaction consists of a mixture of three dNTPs and one ddNTP.
D. Self-ligation of a vector with compatible ends can be prevented by treatment with alkaline phosphatase.
Which one of the following options represents a combination of correct statements?
Given below are four DNA sequences and a set of forward and reverse primers for PCR amplification.
| Sequence | Primes | |
| A | 5' ACAATCGT.....ACTAGTAC-3' | FP: 5'-TGTTAG-3' RP: 5'-TAGTAC-3' |
| B | 5' AGTCTTAG.....ATGCCAGT - 3' | FP: 5'-AAGACT-3' RP: 5'-ACTGGC-3' |
| C | 5' CTTGACTA.....GTACAGTCA-3' | FP: 5'-CTTGAC-3' RP: 5'-TGACTG-3' |
| D | D 5' GATCTAGC.....TCAAGCAGAC-3' | FP: 5'-GATCTA-3' RP: 5'-CAGACG-3' |