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BSc Biotechnology Sem VI 2016 17 2016-17 Biotech Pri. Of Gene Cloning Question Paper - Mumbai University | munotes

T.Y.B.Sc. Biotech Pri. Of Gene Cloning Sem VI 2016 17.pdf
SEM VI · 2016-17 · 1 May 2025

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Questions asked in this paper

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  • N.B: 1. Attempt all questions
  1. Q2 All questions carry equal marks
    • a. Give an example of the following: (any three) 3
    • i) Cofactor required for T4 ligase
    • ii) | Source of Alkaline phosphatase
    • iii) DNase
    • iv) used for probe labelling
    • v) Enzymatic reaction exhibited by Polynucleotide kinase
    • b. Answer of the following: (any two) 12
    • i) | Give an account of nature of cut ends generated by restriction endonucleases
    • ii) | What are linkers and adapters? State their role in rDNA technology
    • iii) Comment: Terminal Transferase has many applications
    • iv) Elaborate on the different applications of T4 DNA polymerase
  2. Q2 a. Explain the following terms: (any three) 3 marks
    • iv). T-DNA
    • b. Attempt the following: (any two) 12
    • i) pBR322 is an ideal cloning vector. Justify
    • ii) an account of: Lambda phage as a vector
    • iii) Explain the construction of M13 phage based vectors
    • iv) Describe binary cloning vector with the help of a neat labeled diagram
  3. Q3 a. Give the importance of the following: (any three) 3 marks
    • vi) ddNTP
    • Q.P. Code :01672
    • b. Give an account of the following: (any two) 12
    • i) | Construction of genomic DNA library
    • ii) Identification of clones in cDNA library
    • iii) fingerprinting
    • iv) Any two types of PCR
  4. Q4 a. State the significance of the following: (any three) ii) 3 marks
    • iii) Islet of Langerhans
    • b. Discuss the following: (any two) 12
    • i) Limitations of traditional methods of vaccine production
    • ii) | Attenuated vaccine for Cholera
    • iv) Diagnosis of Sickle cell anemia
  5. Q5 Write short notes of the following: (any three) 15 marks
    • i) and applications of PCR
    • ii) Features of an ideal cloning vector of reverse transcriptase in rDNA technology
    • v) Klenow fragment

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