TLS Online TPP Program

#Question id: 5732


Consider a plant, such as maize, heterozygous for a paracentric inversion. The inversion is very small and a synapsed inversion loop does not occur in any of the cells. Which of the following statement is correct?

#Part-B Specialized Branches in Biotechnology
  1. All of the gametes should be euploid and consequently viable

  2. All of the recombinant gametes should be deletion and consequently nonviable

  3. All of the gametes should be deletion and consequently nonviable

  4. All of the parental gametes should be deletion and consequently nonviable

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TLS Online TPP Program

#Question id: 19844

#Part-A Aptitude & General Biotechnology

Match the following column, which correctly represent the qPCR done by three methods and measure such as;

                  COLUMN I

                    COLUMN II

A) SYBR green

i) Annealing

B) Taqman Assay

ii) Denaturation

C) Molecular beacon

iii) pH

 

iv) Amplification

 

v) Extension

TLS Online TPP Program

#Question id: 19844

#Part-A Aptitude & General Biotechnology

Match the following column, which correctly represent the qPCR done by three methods and measure such as;

                  COLUMN I

                    COLUMN II

A) SYBR green

i) Annealing

B) Taqman Assay

ii) Denaturation

C) Molecular beacon

iii) pH

 

iv) Amplification

 

v) Extension

TLS Online TPP Program

#Question id: 19845

#Part-A Aptitude & General Biotechnology

SYBR Green qPCR method is based on____I_______ with the _____II______ relationship.

TLS Online TPP Program

#Question id: 19845

#Part-A Aptitude & General Biotechnology

SYBR Green qPCR method is based on____I_______ with the _____II______ relationship.

TLS Online TPP Program

#Question id: 19846

#Part-A Aptitude & General Biotechnology

Variants of PCR has been developed on the basis of___

TLS Online TPP Program

#Question id: 19865

#Part-A Aptitude & General Biotechnology

Match the following activity of variants in Column I with their variants of PCR in Column II given below;

                     COLUMN I

                        COLUMN II

 

A) Enhance efficiency

 

i) Multiplex PCR

 

B) Sequence specific amplification

 

ii) Hot-start PCR

 

C) Mutational analysis

 

iii) Megaprimer PCR

 

 

iv) qPCR with SYBR

 

 

v) AS-PCR

 

 

vi) RLM-RACE