Category: mtx2

buffer protein, Free Radical Generation in Far-UV Synchrotron Radiation Circular Dichroism Assays-Protein and Buffer Composition Contribution

Free Radical Generation in Far-UV Synchrotron Radiation Circular Dichroism Assays-Protein and Buffer Composition ContributionFree Radical Generation in Far-UV Synchrotron Radiation Circular Dichroism Assays-Protein and Buffer Composition Contribution

A great tool to investigate the ligands and/or environmental contribution to protein stability is represented by the Synchrotron Radiation Round Dichroism UV-denaturation assay that consists within the acquisition of a

transfection pei, Large-Scale Transient Production in ExpiCHO-S™ with Enhanced N-Galactosylation-Sialylation and PEI-Based Transfection

Large-Scale Transient Production in ExpiCHO-S™ with Enhanced N-Galactosylation-Sialylation and PEI-Based TransfectionLarge-Scale Transient Production in ExpiCHO-S™ with Enhanced N-Galactosylation-Sialylation and PEI-Based Transfection

Massive-scale transient expression in Chinese language Hamster Ovary (CHO) cells offers a fast protein manufacturing methodology with a possible start-to-end alignment benefit for biotherapeutics drug discovery. On this chapter, experimental

arf1 antibody, Cell-matrix adhesion controls Golgi organization and function through Arf1 activation in anchorage-dependent cells.

Cell-matrix adhesion controls Golgi organization and function through Arf1 activation in anchorage-dependent cells.Cell-matrix adhesion controls Golgi organization and function through Arf1 activation in anchorage-dependent cells.

Cell-matrix adhesion regulates membrane trafficking controlling anchorage-dependent signaling. Whereas a dynamic Golgi advanced can contribute to this pathway, its regulation by adhesion stays unclear. Right here we report that lack

primers

Lipidation of Class IV CdiA Effector Proteins Promotes Target Cell Recognition during Contact-Dependent Growth InhibitionLipidation of Class IV CdiA Effector Proteins Promotes Target Cell Recognition during Contact-Dependent Growth Inhibition

Contact-dependent growth inhibition (CDI) systems enable the direct transfer of protein toxins between competing Gram-negative bacteria. CDI+ strains produce cell surface CdiA effector proteins that bind specific receptors on neighboring bacteria