हिंदी

The recognition sequence of restriction enzymes is generally ______ nucleotide long.

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प्रश्न

The recognition sequence of restriction enzymes is generally ______ nucleotide long.

विकल्प

  • 2 to 4

  • 4 to 8

  • 8 to 10

  • 14 to 18

MCQ
रिक्त स्थान भरें
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उत्तर

The recognition sequence of restriction enzymes is generally 4 to 8 nucleotides long.

Explanation:

The sequences recognized by restriction enzymes are 4 to 8 nucleotides long and characterized by a particular type of internal symmetry. Consider the specific sequence recognized by the enzyme EcoRI.

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अध्याय 12: Biotechnology - Exercises [पृष्ठ २९१]

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बालभारती Biology [English] Standard 12 Maharashtra State Board
अध्याय 12 Biotechnology
Exercises | Q 1.6 | पृष्ठ २९१

संबंधित प्रश्न

What are the restriction endonucleases? Give the rules of their nomenclature.


Identify the characterization techniques that are based on molecular weights of compounds.


Which of the following device is required for PCR?


The following identifies the major features of technology that differentiate modem biotechnology from classical biotechnology.

i. Capability of science to change the genetic material for getting new specific products through rDNA technology, polymerase chain reaction (PCR), microarrays, cell culture and fusion, and bioprocessing.

ii. Ownership of technology and its sociopolitical impact.

iii. Modem biotechnology makes use of only fermentation technology.

iv. Classical biotechnology relies only on principles of plant and animal tissue culture. 


In which of the following techniques, charged molecules (DNA, RNA and Proteins) are separated by applying the electric field?


Which of the following is NOT involved in genetic engineering technique?

i. Combining genes from two organisms

ii. Gene cloning

iii. Transfer of lipid molecules

iv. Transfer of genes to new organisms

v. Repairing or replacing the defective genes by healthy genes

vi. Artificial synthesis of new gene


Match the column I (PCR steps) and Column II (Temperature). Select the correct option.

  Column I (PCR steps)   Column II (Temperature)
i. Polymerization P. 40 - 60°C
ii. Denaturation Q. 70 - 75°C
iii. Primer annealing R. 90 - 98°C
    S. 28 - 37°C

The main reason for the presence of both a leading and a lagging strand during DNA replication is, ______ 


Which of these are most widely used in genetic engineering?


How does the concept of cloning relate to the multiplication of genetic material in biotechnology?


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