TLS Online TPP Program

#Question id: 18980


The most widely used strong regulatable promoters are those

#Part-A Aptitude & General Biotechnology
  1. E.coli lac 
  2. trp (tryptophan)
  3. pL, promoter from bacteriophage
  4. All are regulatable promoters 
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TLS Online TPP Program

#Question id: 19883

#Part-A Aptitude & General Biotechnology

Which of the following statements are true regarding rDNA technology?
a) rDNA technology is used to obtain large number of copies of specific DNA fragments
b) rDNA technology is used to obtain large quantities of the protein produced by the concerned gene
c) rDNA technology is used to integrate gene of interest into chromosomes where it express itself

TLS Online TPP Program

#Question id: 19884

#Part-A Aptitude & General Biotechnology

The first successful transformation of rDNA molecules into a bacterium was carried out by

TLS Online TPP Program

#Question id: 19885

#Part-A Aptitude & General Biotechnology

The plasmid used by Cohen and Boyer fr their transformation experiment was

TLS Online TPP Program

#Question id: 19886

#Part-A Aptitude & General Biotechnology

Gene cloning refers to the
I) Production of large number of copies of the gene being cloned
II) Production of asexual progeny from a single individual or a cell 
III) Mechanism of intake of DNA fragments from the surrounding medium by a cell

TLS Online TPP Program

#Question id: 19887

#Part-A Aptitude & General Biotechnology

Paul Berg’s gene splicing experiment created the first rDNA molecules which was a

TLS Online TPP Program

#Question id: 19888

#Part-A Aptitude & General Biotechnology

There are some typical enzyme used in the manipulation of nucleic acid;

                 

                 ENZYMES

 

USE IN NUCLEIC ACID MANIPULATION

 

A) klenow

 

i) DNA-dependent RNA polymerase

 

B) T4 DNA polymerase

 

ii) Single-strand specific nuclease

 

C) Taq DNA polymerase

 

iii) DNA pol I lacks 5’→ 3’ exonuclease activity

 

D) T7 RNA polymerase

 

iv) Thermostable DNA polymerase used in PCR

 

E) S1 nuclease

 

v) Lack  5’→ 3’ exonuclease activity