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प्रश्न
Name and describe the technique that helps in separation of DNA fragments.
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उत्तर
The fragments can be separated by a technique called gel electrophoresis.
Steps are as follows:
- Step: 1. The DNA fragments are loaded on a gel or matrix and an electric current is applied. The most commonly used matrix is agarose which is a natural polymer extracted from seaweeds.
- Step: 2. Since DNA fragments are negatively charged they move towards the positive charge i.e. anode under an electric field through a gel.
- Step: 3. The DNA fragments move through the gel and separate according to their size. The bigger ones move slowly and the smaller ones move faster.
- Step: 4. The separated fragments can be visualized after staining the DNA with Ethidium bromide followed by exposure to UV radiation. The DNA fragments can be seen as bright orange coloured bands in UV light.
- Step: 5. The separated bands are cut from the agarose gel and extracted from the gel piece.
- Step: 6. DNA fragments purified in this way are used for constructing rDNA after joining them with cloning vectors.
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संबंधित प्रश्न
Rearrange the following in the correct sequence to accomplish an important biological reaction:
(a) In vitro synthesis of copies of DNA of interest
(b) Chemically synthesized oligonucleotides
(c) Enzyme DNA-polymerase
(d) Complementary region of DNA
(e) Genomic DNA template
(f) Nucleotides provided
(g) Primers
(h) Thermostable DNA-polymerase (from Thermus aquaticus)
(i) Denaturation of ds-DNA
Define vector? write any two examples,
Vectors are ____________ molecules that carry a foreign gene and replicate inside the host cell.
DNA polymerase enzyme used in PCR is isolated from ____________ bacteria.
In which of the following techniques, charged molecules (DNA, RNA and Proteins) are separated by applying the electric field?
In PCR technique, the organism providing thermostable DNA polymerase is a ____________.
Exonuclease performs the function of ____________.
A hind of biotechnology involving manipulation of DNA is ______.
Which of the following is not required in the preparation of a recombinant DNA molecule?
What are the different types of electrophoresis?
