In this study, Hammer et al. highlight cyclic‐arginine surface engineering as a highly biocompatible, controllable, and concentration‐dependent regulator of intravitreal nanoparticle mobility in vivo in a translational large animal model. The cyclic arginine surface‐modification supports the development of next‐generation biomaterials for long‐acting ...
Maximilian Hammer +12 more
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Reply to "comment on: Vegetable peptones as a fetal bovine serum substitute in human deciduous tooth pulp stem cell culture". [PDF]
Trevizani M +6 more
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Evaluation of two human diagnostic agarose gel electrophoresis kits for bovine serum protein fractionation. [PDF]
Yamagishi N +7 more
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Reducing Foetal Bovine Serum Culture Conditions does not affect GPCR Signalling
Pearce A +8 more
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Fetal bovine serum: how to leave it behind in the pursuit of more reliable science. [PDF]
Weber T +12 more
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Effect of whey protein hydrolysate isolation as a partial replacement of fetal bovine serum on proliferation and differentiation of Hanwoo primary muscle cells. [PDF]
Lee SH, Park S, Jang S, Park G, Choi J.
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Selective colorimetric sensing of Fe<sup>3+</sup> by hesperetin-conjugated silver nanoparticles: further investigation of interaction properties with bovine serum albumin. [PDF]
Sushma, Chauhan D, Ghosh KS.
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Protein-Modulated Stimuli-Responsive Hydrogels Based on Methacrylated Bovine Serum Albumin and pNIPAm: pH- and Temperature-Dependent Drug Release Behavior. [PDF]
Sennaroglu Bostan M.
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Effects of Resin or Charcoal Treatment on Fetal Bovine Serum and Bovine Calf Serum
Endocrine Research, 2009Charcoal- or resin-stripping of fetal bovine serum (FBS) or bovine calf serum (BCS) intended for supplementation of cell culture media is widely practiced to remove a variety of endogenous compounds, including steroid, peptide, and thyroid hormones.
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Putrescine-oxidase activity in adult bovine serum and fetal bovine serum
In Vitro, 1979Putrescine-oxidase activity was found in fetal bovine serum (FBS) with a pH optimum of 8.0 and in adult bovine serum (ABS) with a pH optimum of 9.8. The crude FBS enzyme had a KM for putrescine of 2.58 x 10(-6) M and a Vmax of 0.53 nmol per hr per 50 microliter serum.
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