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

Persian Verion

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

video

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

sound

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

Persian Version

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

View:

1,631
Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

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

Cites:

Information Journal Paper

Title

CLONING AND EXPRESSION OF HUMAN IL-11 IN E. COLI

Pages

  353-359

Abstract

 Objectives: Interleukin-11 (IL-11) is a thrombopoietic growth factor that stimulates the proliferation of hematopoietic stem cells and megakaryocytes and induces megakaryocyte maturation resulting in increased platelet production. IL-11 has recently been approved for treatment of chemotherapy induced thrombocytopenia in cancer patients. This cytokine is the first growth factor that gained FDA approval for this application. The aim of this study was cloning and RECOMBINANT EXPRESSION of HUMAN IL-11 in E. COLI. Methods: RNA was extracted from a human bone marrow sample and used for cDNA synthesis. cDNA was applied for amplification of IL-11 gene by PCR. The PCR product was cloned, sequenced and expressed in E. COLI using pET28a expression vector. Results: Amplification of HUMAN IL-11 gene using primers designed on mature full length coding region of IL-11 resulted in a 531 bp fragment as visualized by agarose gel electrophoresis. Sequencing of the cloned fragment confirmed the identity of sequence of cloned gene. Expression by pET28a vector resulted in a high level production of recombinant IL-11 which appeared as a 24 kDa protein in the SDS-PAGE analysis of induced culture. Conclusion: The result of the present study indicated that the E .coli expression system is a suitable expression system for RECOMBINANT EXPRESSION of HUMAN IL-11 and could be used for mass production of this cytokine due to high-density cell growth and fast product formation.

Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    FARAJNIA, SAFAR, HASANPOUR, R., & LOTFIPOUR, F.. (2010). CLONING AND EXPRESSION OF HUMAN IL-11 IN E. COLI. PHARMACEUTICAL SCIENCES, 15(4), 353-359. SID. https://sid.ir/paper/48538/en

    Vancouver: Copy

    FARAJNIA SAFAR, HASANPOUR R., LOTFIPOUR F.. CLONING AND EXPRESSION OF HUMAN IL-11 IN E. COLI. PHARMACEUTICAL SCIENCES[Internet]. 2010;15(4):353-359. Available from: https://sid.ir/paper/48538/en

    IEEE: Copy

    SAFAR FARAJNIA, R. HASANPOUR, and F. LOTFIPOUR, “CLONING AND EXPRESSION OF HUMAN IL-11 IN E. COLI,” PHARMACEUTICAL SCIENCES, vol. 15, no. 4, pp. 353–359, 2010, [Online]. Available: https://sid.ir/paper/48538/en

    Related Journal Papers

    Related Seminar Papers

  • No record.
  • Related Plans

  • No record.
  • Recommended Workshops






    Move to top