Robust approaches to the creation of diversity, construction of yeast libraries, and library screening or selection have been elaborated, improving the quality of engineered molecules and certainty of success in an antibody engineering campaign and positioning yeast display as one of the premier antibody engineering technologies currently in use.
However, the quality of engineered myocardial tissues remains poor.
Thus, it is essential to utilize physiological stimuli to improve the quality of engineered constructs.
Benchmark reference information is necessary to assess the quality of engineered cartilage.
The characteristics of scaffolds such as pore structure, surface, and mechanical properties determine the quality of engineered tissues.
Cell morphology and the quality of engineered tissue were evaluated by scanning electron microscopy, histopathology and biochemical methods.
Findings from this study confirm that the polymerization mechanism and network structure have long-term effects on the quality of engineered cartilage, especially under mechanical loading.
In this study two methods based on atomic force microscopy (AFM) were applied to obtain information about the quality of engineered graft surfaces.
By enabling reproducible and controlled changes of specific environmental factors, bioreactor systems provide both the technological means to reveal fundamental mechanisms of cell function in a 3D environment, and the potential to improve the quality of engineered tissues.
