TLS Online TPP Program

#Question id: 4354


Which of the following statements correctly describes the primary difference between enhancers and proximal control elements?

#Part-A Aptitude & General Biotechnology
  1. Enhancers are transcription factors; proximal control elements are DNA sequences.

  2. Enhancers improve transcription; proximal control elements inhibit transcription.

  3. Enhancers are located considerable distances from the promoter; proximal control elements are close to the promoter.

  4. Enhancers are DNA sequences; proximal control elements are proteins.

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TLS Online TPP Program

#Question id: 19789

#Part-A Aptitude & General Biotechnology

How to determine the size of PCR product?

TLS Online TPP Program

#Question id: 19789

#Part-B Specialized Branches in Biotechnology

How to determine the size of PCR product?

TLS Online TPP Program

#Question id: 19790

#Part-A Aptitude & General Biotechnology

What will be the major difference between the PCR and replication is?

TLS Online TPP Program

#Question id: 19790

#Part-A Aptitude & General Biotechnology

What will be the major difference between the PCR and replication is?

TLS Online TPP Program

#Question id: 19791

#Part-A Aptitude & General Biotechnology

Which of the following statements about polymerase chain reaction is correct?
a) PCR denaturation temperature calculated by using Y = X (1+E)n
b) Size of the primer negatively affects the efficiency of PCR
c) Standard PCR doesn’t efficiently amplify sequence much longer than about 5kb.
d) Primer annealing of PCR at 550C for 1.5 min.
e) Time taken for each cycle of PCR considerably longer than 3 min.

TLS Online TPP Program

#Question id: 19791

#Part-A Aptitude & General Biotechnology

Which of the following statements about polymerase chain reaction is correct?
a) PCR denaturation temperature calculated by using Y = X (1+E)n
b) Size of the primer negatively affects the efficiency of PCR
c) Standard PCR doesn’t efficiently amplify sequence much longer than about 5kb.
d) Primer annealing of PCR at 550C for 1.5 min.
e) Time taken for each cycle of PCR considerably longer than 3 min.