DNA strands on a gel, stained with ethidium bromide, when viewed under UV radiation, appear as:
1. | Dark red bands | 2. | Bright blue bands |
3. | Yellow bands | 4. | Bright orange bands |
Which of the following is a correct sequence of steps in a PCR (Polymerase Chain Reaction)?
1. Extension, Denaturation, Annealing
2. Annealing, Denaturation, Extension
3. Denaturation, Annealing, Extension
4. Denaturation, Extension, Annealing
During the purification process for recombinant DNA technology, addition of chilled ethanol precipitates out:
1. | Histones | 2. | Polysaccharides |
3. | RNA | 4. | DNA |
Plasmid pBR322 has a PstI restriction enzyme site within gene ampR that confers ampicillin resistance. If this enzyme is used for inserting a gene for -galactoside production and the recombinant plasmid is inserted in an E.coli strain,
1. | it will lead to the lysis of host cells. |
2. | it will be able to produce a novel protein with dual abilities. |
3. | it will not be able to confer ampicillin resistance to the host cell. |
4. | the transformed cells will have the ability to resist ampicillin as well as produce β -galactoside. |
A specific recognition sequence identified by endonucleases to make cuts at specific positions within the DNA is:
1. Palindromic Nucleotide sequences
2. Poly(A) tail sequences
3. Degenerate primer sequence
4. Okazaki sequences
During the process of gene amplification using PCR, if a very high temperature is not maintained in the beginning, then which of the following PCR will be affected first?
1. | Denaturation | 2. | Ligation |
3. | Annealing | 4. | Extension |
The figure below shows three steps (A, B, C) of Polymerase Chain Reaction (PCR). Select the option giving correct identification together with what it represents.
1. | A - Denaturation at a temperature of about 50ºC |
2. | C - Extension in the presence of heat-stable DNA polymerase |
3. | A - Annealing with two sets of primers |
4. | B - Denaturation at a temperature of about 98ºC separating the two DNA strands |
Select the correct statement from the following:
1. | Gel electrophoresis is used for the amplification of a DNA segment. |
2. | The polymerase enzyme joins the gene of interest and the vector DNA. |
3. | Restriction enzyme digestions are performed by incubating purified DNA molecules with the restriction enzymes of optimum conditions. |
4. | PCR is used for the isolation and separation of genes of interest. |
Spooling is:
1. | Amplification of DNA |
2. | Cutting of separated DNA bands from the agarose gel |
3. | Transfer of separated DNA fragments to synthetic membranes |
4. | Collection of isolated DNA |
In a mixture, DNA fragments are separated by-
1. Bioprocess engineering
2. Restriction digestion
3. Electrophoresis
4. Polymerase chain reaction