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MCQs

Total Questions : 72 | Page 2 of 8 pages
Question 11. Which can be used as a precaution in order to minimize contamination?
  1.    Careful use and design of pipettes
  2.    Placing the pre-PCR and post-PCR stages in the same rooms
  3.    Extracting the DNA along with surface layers
  4.    Use of primers carefully is not very important
 Discuss Question
Answer: Option A. -> Careful use and design of pipettes
Answer: (a).Careful use and design of pipettes
Question 12. How can the specificity of primer annealing be increased?
  1.    Use of short primers
  2.    Raising temperature
  3.    Adjusting the concentration of sodium ions
  4.    Using polymerase with proof reading activity
 Discuss Question
Answer: Option B. -> Raising temperature
Answer: (b).Raising temperature
Question 13. There are basically two types of contamination, laboratory and external. If a PCR product is found to be contaminated by bacteria. It comes under laboratory contamination.
  1.    True
  2.    False
  3.    May be True or False
  4.    Can't say
 Discuss Question
Answer: Option B. -> False
Answer: (b).False
Question 14. Which of the statement holds for long-range PCR and in its relation?
  1.    It is the PCR in which longer templates are used
  2.    DNA polymerases which don’t have proof-reading activity give larger products
  3.    DNA polymerases’ processivity is not a measure to have larger products
  4.    It is PCR in which a mixture of enzymes is used to have larger products
 Discuss Question
Answer: Option D. -> It is PCR in which a mixture of enzymes is used to have larger products
Answer: (d).It is PCR in which a mixture of enzymes is used to have larger products
Question 15. Which of the following conditions don’t contribute to wrong annealing to primer?
  1.    Chance complementarity
  2.    Conditions of annealing
  3.    The original sequence of the primers
  4.    Both the conditions of annealing and the original sequence don’t play any role
 Discuss Question
Answer: Option D. -> Both the conditions of annealing and the original sequence don’t play any role
Answer: (d).Both the conditions of annealing and the original sequence don’t play any role
Question 16. The process of amplification of specific DNA sequences by an enzymatic process is termed as ____________
  1.    amplification
  2.    polymerase chain reaction (PCR)
  3.    translation
  4.    microarrays
 Discuss Question
Answer: Option A. -> amplification
Answer: (a).amplification
Question 17. These are steps taken in carrying out the PCR reaction:
i) Attaching of primers by cooling
ii) Denaturation of strands
iii) DNA synthesis
iv) Heating
Which is the correct order?
(Mentioned from starting to ending the reaction)
  1.    i)-ii)-iii)-iv)
  2.    ii)-i)-iii)-iv)
  3.    iv)-iii)-ii)-i)
  4.    iv)-ii)-i)-iii)
 Discuss Question
Answer: Option D. -> iv)-ii)-i)-iii)
Answer: (d).iv)-ii)-i)-iii)
Question 18. What are primers?
  1.    Primers are the short sequences at the end of the nucleotide sequences which are used for amplification
  2.    Primers are the short sequences which are complementary to the nucleotides at the end of the sequence which is to be amplified
  3.    Primers are the short sequences present anywhere in the nucleotide sequence to be amplified
  4.    Primers are the short sequences which are complementary to the nucleotides anywhere in the sequence to be amplified
 Discuss Question
Answer: Option B. -> Primers are the short sequences which are complementary to the nucleotides at the end of the sequence which is to be amplified
Answer: (b).Primers are the short sequences which are complementary to the nucleotides at the end of the sequence which is to be amplified
Question 19. A reaction mixture for PCR consists of ____________
  1.    heat unstable polymerase
  2.    primers in a limited amount
  3.    deoxynucleoside triphosphate (dNTPs)
  4.    a region complementary to the sequence to be amplified
 Discuss Question
Answer: Option C. -> deoxynucleoside triphosphate (dNTPs)
Answer: (c).deoxynucleoside triphosphate (dNTPs)
Question 20. Which of the following is a characteristic of Taq polymerase?
  1.    It is an RNA polymerase
  2.    It is heat stable
  3.    It is obtained from thermophilic bacterium and can be grown in the laboratory below a temperature of 75 degrees
  4.    It is used in cellular synthesis processes and the optimum temperature is at least 90 degrees
 Discuss Question
Answer: Option B. -> It is heat stable
Answer: (b).It is heat stable

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