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:

364
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

ACTINIDIN A NEW COLLAGENASE FOR ISOLATION AND PRIMARY CULTURE OF THYMIC EPITHELIAL CELLS FROM RAT THYMUS

Pages

  109-109

Abstract

 Objective: Proteolytic enzymes, specially COLLAGENASE, are used to digest exteracellular matrix, cells isolation and primary culture. It is important to find new sources of plant or animal protease instead of bacterial or tissue COLLAGENASE. In the present research, ACTINIDIN, a plentiful protease in KIWIFRUIT (ACTINIDIN deliciosa), was used for isolation and culture of cells from THYMIC EPITHELIAL CELLS (TEC) from rat thymus.Materials and Methods: Materials and Methods: The thymus was taken out. The gland was minced into small pieces and suspended in the PBS containing 1, 2, 4, 8, or 16 mg/ml ACTINIDIN for 1, 2, 3, or 4 h with gentle shaking. The cell pellet was resuspended in William’s E culture medium. The cell suspensions were cultured in dishes precoated with collagen.Results: Rat TEC was properly isolated after digestion of thymus in 4 mg/ml ACTINIDIN for 4 h at 37oC. The isolated cells were adhered to collagen precoated dishes after washing. After 24 h of culture, the adherent cells were flattened and showed polygonal morphology with small nuclei. The viability of the cells as judged by the trypan blue test was estimated to be 90–95% in all isolations.Conclusion: The results showed that ACTINIDIN has not toxic effect on separated cells and is a novel and suitable protease for isolation of rat TEC.

Multimedia

  • No record.
  • Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    SHIRVANI FARSANI, Z., MOSTAFAEI, ALI, MANSOURI, K., & BIDMESHKIPOUR, A.. (2009). ACTINIDIN A NEW COLLAGENASE FOR ISOLATION AND PRIMARY CULTURE OF THYMIC EPITHELIAL CELLS FROM RAT THYMUS. CELL JOURNAL (YAKHTEH), 11(SUPPL. 1), 109-109. SID. https://sid.ir/paper/548079/en

    Vancouver: Copy

    SHIRVANI FARSANI Z., MOSTAFAEI ALI, MANSOURI K., BIDMESHKIPOUR A.. ACTINIDIN A NEW COLLAGENASE FOR ISOLATION AND PRIMARY CULTURE OF THYMIC EPITHELIAL CELLS FROM RAT THYMUS. CELL JOURNAL (YAKHTEH)[Internet]. 2009;11(SUPPL. 1):109-109. Available from: https://sid.ir/paper/548079/en

    IEEE: Copy

    Z. SHIRVANI FARSANI, ALI MOSTAFAEI, K. MANSOURI, and A. BIDMESHKIPOUR, “ACTINIDIN A NEW COLLAGENASE FOR ISOLATION AND PRIMARY CULTURE OF THYMIC EPITHELIAL CELLS FROM RAT THYMUS,” CELL JOURNAL (YAKHTEH), vol. 11, no. SUPPL. 1, pp. 109–109, 2009, [Online]. Available: https://sid.ir/paper/548079/en

    Related Journal Papers

  • No record.
  • Related Seminar Papers

  • No record.
  • Related Plans

  • No record.
  • Recommended Workshops






    مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources
    مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources
    مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources
    مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources
    مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources
    File Not Exists.
    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