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MCQs

Total Questions : 72 | Page 5 of 8 pages
Question 41. Primers are generally ____________
  1.    20-30 nucleotides long
  2.    40-50 nucleotides long
  3.    as long as the template is
  4.    taken according to the amount available
 Discuss Question
Answer: Option A. -> 20-30 nucleotides long
Answer: (a).20-30 nucleotides long
Question 42. Which end of the primer should be matched properly in order to carry out the amplification?
  1.    5’ end
  2.    3’ end
  3.    Both of the ends should be matched properly
  4.    Anyone of the ends should match
 Discuss Question
Answer: Option B. -> 3’ end
Answer: (b).3’ end
Question 43. Melting temperature is given by ____________
  1.    4(G+C) + 2(A+T)
  2.    2(G+C) + 4(A+T)
  3.    2(A+G) + 4(C+T)
  4.    4(A+G) + 2(C+T)
 Discuss Question
Answer: Option A. -> 4(G+C) + 2(A+T)
Answer: (a).4(G+C) + 2(A+T)
Question 44. Both the primers, the start primer and the end primer should have a nearly same melting temperature.
  1.    True
  2.    False
  3.    May be True or False
  4.    Can't say
 Discuss Question
Answer: Option A. -> True
Answer: (a).True
Question 45. Which of the following nucleotides should be there at 3’ end?
  1.    Any of A, T, G or C will work out
  2.    Either A or T
  3.    Either G or C
  4.    Specifically G
 Discuss Question
Answer: Option C. -> Either G or C
Answer: (c).Either G or C
Question 46. In the case of uncertainty, if more than one nucleotide is included at a position it is called ____________
  1.    mixed site
  2.    polynucleotide site
  3.    unique site
  4.    degenerate site
 Discuss Question
Answer: Option A. -> mixed site
Answer: (a).mixed site
Question 47. What is the property of inosine?
  1.    Having narrow range of pairing capabilities
  2.    Having a broad range of pairing capabilities
  3.    The pairing capability is the same as the normal nucleotides
  4.    It is abbreviated as A
 Discuss Question
Answer: Option B. -> Having a broad range of pairing capabilities
Answer: (b).Having a broad range of pairing capabilities
Question 48. Why internal secondary structures are not preferred for primers?
  1.    Internal structures are very bulky and thus elongation is not preferred
  2.    Because of it, primer may fold back on itself and won’t be available for template
  3.    Internal secondary structures require more amount of template
  4.    If internal structures are present, no proof reading would be observed
 Discuss Question
Answer: Option B. -> Because of it, primer may fold back on itself and won’t be available for template
Answer: (b).Because of it, primer may fold back on itself and won’t be available for template
Question 49. What will happen if the amino acid sequence is used directly for primer designing?
  1.    There would be certainty because the genetic code is unique for each amino acid
  2.    There would be uncertainty as the genetic code is degenerate and none of the amino acid is having a unique code
  3.    There would be uncertainty as the genetic code is degenerate but some of the amino acids such as methionine are having a unique codon
  4.    The amount of uncertainty or certainty is a matter of chance
 Discuss Question
Answer: Option C. -> There would be uncertainty as the genetic code is degenerate but some of the amino acids such as methionine are having a unique codon
Answer: (c).There would be uncertainty as the genetic code is degenerate but some of the amino acids such as methionine are having a unique codon
Question 50. Which of the following is favoured for primer design?
  1.    The melting temperature should be different for both the primers
  2.    Primers should be long in length
  3.    Primers should not be complementary to each other
  4.    Matching should be of whole primer to the template
 Discuss Question
Answer: Option C. -> Primers should not be complementary to each other
Answer: (c).Primers should not be complementary to each other

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