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BSc Biotechnology Sem IV ATKT 2018-19 ATKT Biotech Molecular Diagnostics Question Paper - Mumbai University | munotes

ATKT Question Paper, 2018.pdf
SEM IV · 1 May 2025

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Questions asked in this paper

  • 1) Attempt all questions
  1. Q2 All questions carry equal marks
  2. Q4 Use of log tables and non-programmable calculator is allowed
  3. Q5 For Q.2,Q.3 and attempt A and B OR Cand D
  4. Q1 Do as directed (Any fifteen) 15 marks
  5. Q1 Give significance of molecular diagnostics
  6. Q2 Give significance of using mixture of phenol and chloroform in DNA
  7. Q3 State the use of proteinase K
  8. Q4 State the significance of polyT or polyU oligomers in mRNA isolation
  9. Q5 How depurination of larger fragment of DNA is is achieved during
  10. Q6 Proteins are separated using
  11. Q7 State true or false: Enzymatical amplification of RNA is called PCR
  12. Q8 Give an application of Taq Pol
  13. Q9 What is UNG?
  14. Q10 Who is the Inventor of PCR?
  15. Q11 Define Forward primer
  16. Q12 State true or false: DNA can be found in aerosol
  17. Q13 Give an application of thermostable DNA ligase 14 State true or false: Exonuclease-I can degrade primers
  18. Q15 Give the full form of VNTR
  19. Q16 State true or false: RFLPs can be used as original molecular targets for gene mapping, human identification, and parentage testing
  20. Q17 In sickle cell anaemia valine is inserted into the polypeptide instead of
  21. Q18 Gonorrhea is caused by the microbe
  22. Q19 State true or false: Fragile X Syndrome leads to Mental Retardation
  23. Q20 Define Clinical Genetics
    • Q.P.Code: 33973
  24. Q2 A_ Explain restriction enzyme mapping. Elaborate on DNA probes and protein probes 07 Explain the initial steps in nucleic acid isolation depending on the nature 08 of the starting material 8 marks
  25. Q2 D_ Explain in detail the DNA transfer methods from gel to membrane. 7 marks
  26. Q3 A_ Explain the process of PCR. Discuss the process of synthesis of cDNA. 07 8 marks
  27. Q3 C is Real time PCR and explain it in detail. 8 marks
  28. Q3 D__ Discuss: Primer designing. Discuss molecular testing for Neisseria. 08 7 marks
  29. Q4 B is an Informed Consent? Mention all the information that should be provided in an Informed Consent Form for Clinical Genetic testing explain the application of RFLP in detection of Sickle 08 7 marks
  30. Q4 D_ Explain the classification of Genetic testing Indications. 7 marks
  31. Q5 Write Short notes on any three of the following 15 marks
    • a. Specimen requirements for HIV viral assays
    • b. Patents relating to molecular diagnostics Physical methods used for control of PCR contamination
    • e. Any one Method used for probe labelling

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