When “sticky ends” are paired, they can be joined by:
1. | restriction enzymes | 2. | polymerases |
3. | methylase | 4. | DNA ligase |
Which of the following is not a plasmid?
1. | pSC101 | 2. | pUC18 |
3. | BamHI | 4. | pBR322 |
Which of the following is normally not used as a method of introduction of foreign DNA into an animal cell?
1. | Microinjection | 2. | Liposomes |
3. | Biolistics | 4. | Transfection |
Which of the given statements is correct in the context of visualizing DNA molecules separated by agarose gel electrophoresis?
1. | DNA can be seen in visible light |
2. | DNA can be seen without staining in visible light |
3. | Ethidium bromide stained DNA can be seen in visible light |
4. | Ethidium bromide stained DNA can be seen under exposure to UV light |
'Restriction' in Restriction enzyme refers to:
1. | Cleaving of the phosphodiester bonds in DNA by the enzyme |
2. | Cutting of DNA at a specific position only |
3. | Prevention of the multiplication of bacteriophage by the host bacteria |
4. | All of the above |
Which of the following is not required in the preparation of a recombinant DNA molecule?
1. | Restriction endonuclease | 2. | DNA ligase |
3. | DNA fragments | 4. | E.coli |
The most important feature in a plasmid to serve as a vector in gene cloning experiment is:
1. | Origin of replication (ori) |
2. | Presence of a selectable marker |
3. | Presence of sites for restriction endonuclease |
4. | Its size |
While isolating DNA from bacteria, which of the following enzymes is not required?
1. | Lysozyme | 2. | Ribonuclease |
3. | Deoxyribonuclease | 4. | Protease |
Which of the following contributed in popularising the PCR (polymerase chain reactions) technique?
1. | Easy availability of DNA template |
2. | Availability of synthetic primers |
3. | Availability of cheap deoxyribonucleotides |
4. | Availability of 'Thermostable' DNA polymerase |
Which of the following steps are catalysed by Taq DNA polymerase in a PCR reaction?
1. Denaturation of template DNA
2. Annealing of primers to template DNA
3. Extension of primer end on the template DNA
4. All of the above