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TLS Online TPP Program

#Question id: 2998

Which of the following statement are correct?

#Section 2: General Biology

  1. The generation time is the reciprocal of the growth rate constant.

  2. In stationary phase, there is no cell division of bacterial cell 

  3. Their rate of growth is rapidly increasing during the exponential phase

  4. The stationary phase is similar to growth in lag phase

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TLS Online TPP Program

#Question id: 12916

#Section 7: Recombinant DNA technology and Other Tools in Biotechnology

Which statement is correct for Zoo blotting?
TLS Online TPP Program

#Question id: 12917

#Section 7: Recombinant DNA technology and Other Tools in Biotechnology

Arrange the steps of stages in PCR in correct order.
1. The region to be specifically amplified is made accessible within the complex DNA.
2. The double stranded DNA is denatured by heating the reaction mixture to above 90 degree Celsius.
3. A thermal cycler is used to incrementally decrease the annealing temperature.
4. Reaction mixture is then cooled to a temperature between 40 and 60 degree celsius.
TLS Online TPP Program

#Question id: 12918

#Section 7: Recombinant DNA technology and Other Tools in Biotechnology

Name the enzyme which helps in the DNA synthesis in the PCR.
TLS Online TPP Program

#Question id: 12919

#Section 7: Recombinant DNA technology and Other Tools in Biotechnology

Which of the following statement is not correct about RT-PCR. 
TLS Online TPP Program

#Question id: 12920

#Section 7: Recombinant DNA technology and Other Tools in Biotechnology

The development of isothermal systems such as the ____ DNA amplification system do away with the need for a thermal cycler and have the advantage of being able to be used outside the laboratory.
TLS Online TPP Program

#Question id: 12921

#Section 7: Recombinant DNA technology and Other Tools in Biotechnology

Match the following:-
A. Gene probe production.              i. Novel proteins
B. Genome mapping.                       ii. PCR mutagenesis
C. Protein Engineering.                 iii. Sequence tagged sites
D. Gene Editing.                                iv. Use with blots