Nanoparticles often cause receptors expressed on specific cells, but several receptors are (i) highly expressive in one cell and (ii) endocytosis involved. One unexplored alternate to manipulate an endocrinologist gene expressed in multiple cell types; The ideal gene prevents cell type delivery than the cell type B, promoting supply of cell type. This requires the supply of nanoparticles to maintain the commonly-endocated genotype, which depends on cell type depending on vivo; It may be unknown. Based on its microorganic regulation, we have taken into consideration Cave1 1 (Cav1) that promotes cell-specific effects on nanoparty supply. Fluorescence was not sensitive enough to investigate this question and, as a result, we developed a platform called QUANT to study nanoparticle biodefection. QUANT is 108It is more sensitive than fluorescence and can be a multiplex. Measurement of how the 226 lipid nanoparticles (LNPs) were seen in nucleic acids in a variety of cells in the wild type and in the Cav1 anti-mash, were characterized by CAV1 variable type specifications. Cav1 knockout has not replaced the LNP supply of lung and kidney macrophages, but significantly reduced LNP supply in Kupffer cells that are liver resident macrophages. This data shows that macrophages are expressed by a kenovically-mediated endocytosis that is tissue type. These results suggest that manipulative receptors expressed in multiple cells can be used for drug use.
Support information is free at the ACS publications website: DOI: 10.1021 / acs.nanolett.8b03149.
DDPCR belt codes, Alexa-647 fluorescence results, 8 nt barcodes and DLS outputs, common ddPCR barcode number, normal nanoptic biodistribution across two screens and QUANT results (PDF)