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HG-6-64-1 in A375, HCT-116, HT-29
HG-6-64-1 in A375, HCT-116, HT-29

... LINCS joint project: a subset of perturbations. Collaboration of LINCS centers means that these perturbations are explored in great detail. • Time-points: series instead of one single time point • Doses: saturating and (multiple) subsaturating concentration. • Cell contexts: extensively characteriz ...
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... Concept 6.5: Mitochondria and chloroplasts change energy from one form to another • Mitochondria are the sites of cellular respiration, a metabolic process that uses oxygen to generate ATP • Chloroplasts, found in plants and algae, are the sites of photosynthesis • Peroxisomes are oxidative organel ...
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... A physiological malfunction in many genetic disorders is elicited by an altered folding determinant in a protein due to a mutation in the gene leading, for example, to an intracellular block, missorting or degradation of this protein (Stein et al., 2002; Bross et al., 1999). Normally, membrane and s ...
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... B.) Your cell must be 3- dimensional with front, back and sides. C.) The model may be made out of any materials that are non-perishable D.) All parts of your cell must be labeled clearly. This can be accomplished in 2 ways: 1) Use toothpicks or straight pins and pieces of paper to make “flag” labels ...
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... how these factors and intracellular signals induce the endothelial transformation is still matter of debate2,16,29. It is known that EGF or transforming growth factor-α (TGF-α) acts by binding to EGFR leading to the receptor homo or hetero-dimerization, activation of its RTK cytosolic domain and aut ...
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Contribution of the Plasma Membrane and Central Vacuole in the
Contribution of the Plasma Membrane and Central Vacuole in the

... endosomes (Ueda et al. 2001). Most of these putative endosomes emerged far away from the perinuclear region where autolysosomes were accumulating. While these putative endosomes possessed a strong fluorescence, the autolysosomes did not show fluorescence with comparable intensity (Fig. 1B; compare f ...
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Cell encapsulation



Cell microencapsulation technology involves immobilization of the cells within a polymeric semi-permeable membrane that permits the bidirectional diffusion of molecules such as the influx of oxygen, nutrients, growth factors etc. essential for cell metabolism and the outward diffusion of waste products and therapeutic proteins. At the same time, the semi-permeable nature of the membrane prevents immune cells and antibodies from destroying the encapsulated cells regarding them as foreign invaders.The main motive of cell encapsulation technology is to overcome the existing problem of graft rejection in tissue engineering applications and thus reduce the need for long-term use of immunosuppressive drugs after an organ transplant to control side effects.
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