TLS Online TPP Program

#Question id: 11411


Vulnerability to extinction can be linked to species following characteristics. Which of the following statement are correct?

 A. Rare species are more prone to extinction than common ones.

 B. Species that are capable of migrating between fragments of habitat, such as between mainland areas and islands, may be more resistant to extinction

 C. Organisms that are specialists are more likely to go extinct

 D. Species with naturally long life spans may be more likely to become extinct

#Unit 10. Ecological Principles
  1. A, B and C
  2. A, C and D
  3. B, C and D
  4. A, B and D
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TLS Online TPP Program

#Question id: 19842

#Unit 13. Methods in Biology

Primer-Dimer leads to the formation of ___
a) Inter-complemetary primers
b) Hybrid 
c) Amplicons

TLS Online TPP Program

#Question id: 19843

#Unit 13. Methods in Biology

Real time PCR analyzed various steps such as__
a) Denaturation
b) Annealing
c) Phosphorylation
d) Amplification
e) Methylation
f) Extension
Which of the following steps are correctly analyzed by real time PCR?

TLS Online TPP Program

#Question id: 19844

#Unit 13. Methods in Biology

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

#Unit 13. Methods in Biology

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

TLS Online TPP Program

#Question id: 19846

#Unit 13. Methods in Biology

Variants of PCR has been developed on the basis of___

TLS Online TPP Program

#Question id: 19865

#Unit 13. Methods in Biology

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