مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Verion

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

video

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

sound

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Version

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View:

776
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

0
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

CLONING INFLUENZA M2E- VIBRIO CHOLERA CTXB FUSION FRAGMENT IN PET28A PLASMID

Pages

  29-35

Abstract

 Aim and background: The extra domain of the M2 protein of INFLUENZA is a weak immunogen, Hence this is not a suitable candidate for the vaccine development. The B subunit of the Cholera enterotoxin is nontoxic causing attachment of the holotoxin to the OMI at the surface of the epithelial intestine cells, while, CTB is highly immunogenic. So FUSION of these two genes would be very applicable in INFLUENZA vaccine development.Material and methods: using PCR with specific primers including restriction sites ctxB was amplified. Standard strain of INFLUENZA type A (AJPUERTO RICO/8/34) was prepared and M2e was amplified using RT-PCR with specific primers. The second PCR reaction was performed for the FUSION of the M2e and ctxB using the F primer of M2e and R primer of ctxB. PCR product was digested with BamHI and EcoRI and cloned into the pET28a. Verification of the cloning was performed using sequence analyzing. After analysis, the recombinant pET28a1M2e-ctxB was transferred into E. coli Top10. The final confirmation was performed using colony PCR, double digesting and sequence analysis.Results: Sequence analysis showed that M2e has been fused to ctxB in an exact frame. Moreover the fused gene was cloned into the restriction site of the BamHI and EcoR1 in pET28a.Conclusion: Despite stability of the sequence of M2e it is not immunogen but FUSION to strong immunogens such as CTB would be a new suggestion for INFLUENZA recombinant vaccine production.

Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    MIRZAEI, NIMA, & REZAEI, FARHAD. (2013). CLONING INFLUENZA M2E- VIBRIO CHOLERA CTXB FUSION FRAGMENT IN PET28A PLASMID. NEW CELLULAR & MOLECULAR BIOTECHNOLOGY JOURNAL, 3(9), 29-35. SID. https://sid.ir/paper/204526/en

    Vancouver: Copy

    MIRZAEI NIMA, REZAEI FARHAD. CLONING INFLUENZA M2E- VIBRIO CHOLERA CTXB FUSION FRAGMENT IN PET28A PLASMID. NEW CELLULAR & MOLECULAR BIOTECHNOLOGY JOURNAL[Internet]. 2013;3(9):29-35. Available from: https://sid.ir/paper/204526/en

    IEEE: Copy

    NIMA MIRZAEI, and FARHAD REZAEI, “CLONING INFLUENZA M2E- VIBRIO CHOLERA CTXB FUSION FRAGMENT IN PET28A PLASMID,” NEW CELLULAR & MOLECULAR BIOTECHNOLOGY JOURNAL, vol. 3, no. 9, pp. 29–35, 2013, [Online]. Available: https://sid.ir/paper/204526/en

    Related Journal Papers

    Related Seminar Papers

  • No record.
  • Related Plans

  • No record.
  • Recommended Workshops






    Move to top
    telegram sharing button
    whatsapp sharing button
    linkedin sharing button
    twitter sharing button
    email sharing button
    email sharing button
    email sharing button
    sharethis sharing button