हिंदी
कर्नाटक बोर्ड पी.यू.सी.पीयूसी विज्ञान 2nd PUC Class 12

Which of the given statements is correct in the context of visualizing DNA molecules separated by agarose gel electrophoresis? - Biology

Advertisements
Advertisements

प्रश्न

Which of the given statements is correct in the context of visualizing DNA molecules separated by agarose gel electrophoresis?

विकल्प

  • DNA can be seen in visible light

  • DNA can be seen without staining in visible light

  • Ethidium bromide stained DNA can be seen in visible light

  • Ethidium bromide stained DNA can be seen under exposure to UV light

MCQ
Advertisements

उत्तर

Ethidium bromide stained DNA can be seen under exposure to UV light

Explanation:

DNA molecules separated by agarose gel electrophoresis are not visible in normal visible light and require staining. Ethidium bromide binds to DNA and fluoresces under UV light, allowing visualization of DNA bands as bright orange coloured bands. This method is widely used in laboratories for DNA analysis after gel electrophoresis.

shaalaa.com
Tools of Recombinant DNA Technology - Restriction Enzymes
  क्या इस प्रश्न या उत्तर में कोई त्रुटि है?
अध्याय 11: Biotechnology : Principles and Processes - MULTIPLE CHOICE QUESTIONS [पृष्ठ ७५]

APPEARS IN

एनसीईआरटी एक्झांप्लर Biology [English] Class 12
अध्याय 11 Biotechnology : Principles and Processes
MULTIPLE CHOICE QUESTIONS | Q 4. | पृष्ठ ७५
नूतन Biology [English] Class 12 ISC
अध्याय 13 Principles and Processes of Biotechnology
Test Your Progress | Q 1. 42. | पृष्ठ ५३१

संबंधित प्रश्न

Why is the enzyme cellulase needed for isolating genetic material from plant cells and not form the animal cells?


Name the enzymes that are used for the isolation of DNA from bacterial and fungal cells for recombinant DNA technology.


How does a restriction nuclease function? Explain


Name and describe the technique that helps in separating the DNA fragments formed by the use of restriction endonuclease


Distinguish between exonuclease and endonuclease.


Answer the following question.
Write the use of restriction endonuclease in the formation of recombinant DNA.


Give a reason why :
Single cloning site is preferred in a vector.


Which of the following radioisotope is not suitable for DNA labeling based studies?


DNA fragments separate according to size through?


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 ______


'Restriction' in Restriction enzyme refers to ______.


In agarose gel electrophoresis, DNA molecules are separated on the basis of their ______.


Which of the following bacteria is not a source of restriction endonuclease?


Which of the following statements does not hold true for restriction enzyme?


Would you choose an exonuclease while producing a recombinant DNA molecule?


Restriction enzymes that are used in the construction of recombinant DNA are endonucleases which cut the DNA at ‘specific-recognition sequence’. What would be the disadvantage if they do not cut the DNA at specific-recognition sequence?


A plasmid DNA and a linear DNA (both are of the same size) have one site for a restriction endonuclease. When cut and separated on agarose gel electrophoresis, plasmid shows one DNA band while linear DNA shows two fragments. Explain.


How does one visualise DNA on an agarose gel?


A mixture of fragmented DNA was electrophoresed in an agarose gel. After staining the gel with ethidium bromide, no DNA bands were observed. What could be the reason?


CTTAAG
GAATTC

  1. What are such sequences called? Name the enzyme used that recognizes such nucleotide sequences.
  2. What is their significance in biotechnology?

Carefully observe the given picture. A mixture of DNA with fragments ranging from 200 base pairs to 2500 base pairs was electrophoresed on agarose gel with the following arrangement.

(a) What result will be obtained on staining with ethidium bromide? Explain with reason.

(b) The above setup was modified and a band with 250 base pairs was obtained at X.

What change(s) were made to the previous design to obtain a band at X? Why did the band appear at position X?


'EcoRI' has played a very significant role in rDNA technology.

  1. Explain the convention for naming EcoRI.
  2. Write the recognition site and the cleavage sites of this restriction endonuclease.

State the principle involved in separation of DNA fragments using gel electrophoresis.


How are DNA fragments visualised once they are separated by gel electrophoresis?


Share
Notifications

Englishहिंदीमराठी


      Forgot password?
Use app×