TLS Online TPP Program

#Question id: 5243


Auxotroph culture (His- and Lac-) culture of E. coli was mutagenised. On what media would one spread the mutagenised cells to select prototroph for both His+  and Lac+ cells?

#SCPH06 I Botany
  1. Minimal media+Histidine

  2. Minimal media+Lactose

  3. Minimal media + Histidine + Lactose 

  4. Minimal media

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TLS Online TPP Program

#Question id: 12920

#SCPH06 I Botany

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: 12920

#SCPH28 | Zoology

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

#SCPH01 Biochemistry

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

TLS Online TPP Program

#Question id: 12921

#SCPH06 I Botany

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

TLS Online TPP Program

#Question id: 12921

#SCPH28 | Zoology

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

TLS Online TPP Program

#Question id: 12922

#SCPH01 Biochemistry

 Match the following:-
1. Ligase chain reaction.              i. Mutation detection
2. Nucleic acid sequence based   amplification.                            ii.Non isothermal                   
3. Loop mediated isothermal amplification.                      iii. Viral detection
4. Branched DNA amplification.   iv.parasitic disease