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Number of recognition sites usually pref...

Number of recognition sites usually preferred for a vector is

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Exergonic reactions are usually:

Which one of the following characteristics is generally not preferred for a cloning vector ? a) An origin of replication b) An antibiotic resistance marker c)Multiple restriction sites d) A high copy number

Read the following statements and select the correct ones. (i) Same kind of sticky ends are produced when a DNA has been cut by different restriction enzymes. (ii) Exonucleases make cuts at specific positions within the DNA. (iii) Hind ll was the first restriction endonuclease to be isolated. (iv) A bacteriophage has the ability to replicate within bacterial cells by integrating its DNA with bacterial DNA. (v) Presence of more than one recognition sites for a enzyme within the vector facilitates the gene cloning.

The number of vectors of unit length perpedicular to the vectors (hat(i)+hat(j))and(hat(j)+hat(k)) is

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NEW JOYTHI PUBLICATION-BIOTECHNOLOGY : PRINCIPLES AND PROCESSES -New Evaluation Type Questions
  1. Separation and isolation of DNA fragments is a major event in recombi-...

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  2. How are the DNA fragments separated through gel electrophoresis ex-tra...

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  3. Name two important cloning vectors .

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  4. What are the main features that are required to facilitate cloning in...

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  5. Explain the significance of origin of replication and selectable marke...

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  6. Name any three suitable 'selectable marker' for E.coli.

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  7. During genetic engineering experiments recombinants are distinguished ...

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  8. DNA is a hydrophilic molecule, so it cannot pass through cell membrane...

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  9. Number of recognition sites usually preferred for a vector is

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  10. You are provided with the mixture of transformed bacteria having recom...

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  11. Agrobacterium tumifaciens act as a natural genetic engineer , who tran...

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  12. Given below are the different steps in recombinant DNA technology. Arr...

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  13. DNA is usually intertwind with histone proteins and RNA. But in geneti...

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  14. Briefly explaing the 'cutting' and 'ligation' of DNA during recombinan...

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  15. One of the methods by which recombinant DNA can be introduced into hos...

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  16. Explain how the gene of interest is amplified invitro during biotechno...

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  17. What is the significance of thermostable DNA polymerase during PCR ? ...

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  18. Distinguish between recombinant DNA and recombinant protein.

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  19. Give the significance of using a 'bioreactor' in biotechnological expe...

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  20. Explain the importance of (a) ori, (b) amp^(R) and (c) rop in the E. c...

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