DNA Technology Flashcards

1
Q

How Recombinant DNA technique is done?

A

This is acheived by using specific restriction enzyme for cutting the DNA INTO SUITble fragments and then joining together the appropriate fragments using DNA ligase enzyme.

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2
Q

Purpose of Recombinant DNA technique?

A

1- to obtain large no. of copies of specific DNA fragments
2- to recover large quantities of the protein produced by the concerned gene
3- to integrate the gene into the chromosome of the target org.

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3
Q

What is a Restriction enzyme?

A

Is an enzyme that cuts the dsDNA at specific recognition nucleotide sequences known as restriction sites.

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4
Q

Restriction enzyme are found in_____?

A

Bacteria

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5
Q

Applications of Restriction enzyme?

A
  • Used to assist insertion of genes into plasmid vectors during gene cloning and protein expression experiments.
  • used to digest genomic DNA for gene analysis by southern blot
  • used to distinguish gene alleles
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6
Q

What is a ‘vector’?

A

Is an agent that can carry a DNA fragment into host cell.

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7
Q

What is ‘ cloning vector’?

A

If the vector is used for reproducing the DNA fragment,it is called a ‘cloning vector’

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8
Q

What is a ‘expression vector’?

A

If vector is used for expressing certain gene in the DNA fragment

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9
Q

The DNA segment,to be cloned is called_____?

A

DNA insert

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10
Q

Write steps of Recombinant DNA TECH/ gene cloning?

A

1- identification and isolation of the desired gene or DNA fragment to be cloned.
2- insertion of isolated gene in a suitable vector
3- introduction of this vector into a suitable org./ cell called host ( transformation )
4- selection of the transformed host cells
5- multiplication/ expression/ integration followed byexpression of the introduced gene in the host.

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11
Q

Explain Recombinant DNA technique?

A

Recombinant DNA technique otherwise called as gene cloning is the technique which facilitate the formation of chimeric DNA by fusing DNAs from different sources.

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