
SynopsisSpiderweb‐like gelatine matrices generated by electrospinning are introduced as versatile substrate for culturing animal cell monolayers destined for cryofixation and EM. Thus, non‐disruptive sampling and transfer of native cells into high‐pressure freezing devices is possible within about 30 seconds. In addition to cryosection‐ and replica‐labelling, this aproach can be applied to various complementary microscopy and biochemical methods.
palmitoyl acyl transferase, Plasmodium berghei, Cell- och molekylärbiologi, Plasmodium falciparum, Amino Acid Motifs, Cell Culture Techniques, Protozoan Proteins, Toxoplasma gondii, Acetyltransferases, 616, Humans, palmitoylation, Phylogeny, Original Articles, invasion, egress, Protein Structure, Tertiary, Protein Transport, rhoptry organelle, Apicomplexa, Genome, Protozoan, Toxoplasma, Cell and Molecular Biology, Gene Deletion, ddc: ddc:616
palmitoyl acyl transferase, Plasmodium berghei, Cell- och molekylärbiologi, Plasmodium falciparum, Amino Acid Motifs, Cell Culture Techniques, Protozoan Proteins, Toxoplasma gondii, Acetyltransferases, 616, Humans, palmitoylation, Phylogeny, Original Articles, invasion, egress, Protein Structure, Tertiary, Protein Transport, rhoptry organelle, Apicomplexa, Genome, Protozoan, Toxoplasma, Cell and Molecular Biology, Gene Deletion, ddc: ddc:616
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