TLS Online TPP Program

#Question id: 14451


What is the difference between Psychrotrophs and Psychrophiles respectively?

#Section 2: General Biology
  1. Can grow at temperature ranges 20-30oC while later cannot grow.
  2. Can grow at temperature ranges 20-30oC while former cannot grow.
  3. Both cannot grow at higher temperature ranging 15- 25 oC.
  4. Both can grow at higher temperature ranging 15- 25 oC.
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TLS Online TPP Program

#Question id: 12938

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

What is the main advantage of using Yeast Artificial Chromosome based vector over other vectors?
1. It has ability to clone very large fragments of DNA.
2. YAC vectors do not contain origin of replication sites 
3. It has insert  range up to 2000 kb.
4. It help in genome mapping and sequencing projects.

TLS Online TPP Program

#Question id: 12939

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

Choose the incorrect statement for the production of site-directed mutations.

TLS Online TPP Program

#Question id: 12940

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

 Choose the correct order for the steps involve in Protein engineering.
1. Protein modelling
2. Protein crystallography
3. Site-directed mutations
4. Comparison with entries in databases of known proteins.

TLS Online TPP Program

#Question id: 12941

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

Name the therapeutic protein which has been used to successfully treat certain types of breast cancer.

TLS Online TPP Program

#Question id: 12942

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

Name a single - stranded uracil containing vector which is grown in a selectable host deficit of the enzymes.

TLS Online TPP Program

#Question id: 12943

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

Choose the correct order for the steps involve in Insitu hybridization.
1. Cell permeaabilisation
2. Detection of hybridised probe radioactive.
3. Wash excess probe from section
4. Cell fixation