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प्रश्न
In agarose gel electrophoresis, DNA molecules are separated on the basis of their ______.
विकल्प
Charge only
Size only
Charge to size ratio
All of the above
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उत्तर
In agarose gel electrophoresis, DNA molecules are separated on the basis of their size only.
Explanation:
The gel acts as a molecular sieve, where smaller DNA fragments migrate faster through the pores of the agarose matrix compared to larger ones. Although DNA molecules are negatively charged and move toward the positive electrode due to their charge, the separation principle hinges predominantly on size differences, not charge alone or charge-to-size ratio.
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संबंधित प्रश्न
Explain with the help of a suitable example the naming of a restriction endonuclease.
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Mention the difference in the mode of action of exonuclease and endonuclease.
How does a restriction nuclease function? Explain
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Restriction Enzymes
The total number of nucleotide sequences of DNA that code for a hormone is 1530. The proportion of different bases in the sequence is found to be Adenine = 34%, Guanine = 19%, Cytosine = 23%, Thymine = 19%.
Applying Chargaff’s rule, what conclusion can be drawn?
The DNA fragment separated on an agarose gel can be visualized by staining with ______.
Restriction enzymes ______.
DNA strands on a gel stained with ethidium bromide when viewed under UV radiation, appear as ______
A specific recognition sequence identified by endonucleases to make cuts at specific positions within the DNA is ______
While isolating DNA from bacteria, which of the following enzymes is not required?
Which of the following bacteria is not a source of restriction endonuclease?
Restriction enzymes should not have more than one site of action in the cloning site of a vector. Comment.
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What is elution?
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- Explain the convention for naming EcoRI.
- Write the recognition site and the cleavage sites of this restriction endonuclease.
In the restriction endonuclease EcoRI, what do the letter 'R' and the Roman numeral 'I' represent?
According to the sieving effect of an agarose gel matrix, which DNA fragments move the farthest and fastest from the loading wells?
What is the process called when desired, separated DNA bands are physically cut out from the agarose gel and extracted from the gel piece?
Why are Type II restriction endonucleases the primary class of restriction enzymes used in genetic manipulation?
