Title of article
Cloning, Expression and Functional Characterization of In-House Prepared Human Basic Fibroblast Growth Factor -
Author/Authors
Rassouli، Hassan نويسنده , , Sharif Tabe Bordbar، Mohammad نويسنده Department of Molecular Systems Biology at Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran , , Rezaei Larijani، Mehran نويسنده Department of Stem Cells and Developmental Biology at Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehra , , Pakzad، Mohammad نويسنده Department of Stem Cells and Developmental Biology at Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehra , , Baharvand، Hossein نويسنده , , Hosseini Salekdeh، Ghasem نويسنده Department of Molecular Systems Biology at Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran ,
Issue Information
دوفصلنامه با شماره پیاپی 56 سال 2013
Pages
10
From page
282
To page
291
Abstract
Objective: Human basic fibroblast growth factor (bFGF) plays an important role in cellular proliferation, embryonic development, and angiogenesis as well as in several signaling pathways of various cell types. bFGF is an essential growth factor for the maintenance of undifferentiated human embryonic stem cells (hESCs) and human induced pluripotent stem cells (hiPSCs).
Materials and Methods: In this experimental study, we present a straightforward method
to produce biologically active recombinant human bFGF protein in E. coli that has long-term storage ability.
Results: This procedure provides a rapid, cost effective purification of a soluble human bFGF protein that is biologically active and functional as measured in hESCs and hiPSCs in vitro and in vivo.
Conclusion: The results show no significant difference in function between our in-house produced and commercialized bFGF.
Journal title
Cell Journal (Yakhteh)
Serial Year
2013
Journal title
Cell Journal (Yakhteh)
Record number
691486
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