{"CIL_CCDB":{"Status":{"Is_public":true,"Deleted":false,"Publish_time":1300248000},"Data_type":{"Still_image":true,"Z_stack":false,"Video":false,"Time_series":false},"CIL":{"Image_files":[{"File_type":"Jpeg","File_path":"12633.jpg","Size":4999134,"Mime_type":"image\/jpeg; charset=utf-8"},{"File_type":"Zip","File_path":"12633.zip","Size":34778274,"Mime_type":"application\/zip"},{"File_type":"OME_tif","File_path":"12633.tif","Size":31400000,"Mime_type":"image\/tif"}],"CORE":{"ATTRIBUTION":{"URLs":[{"Href":"http:\/\/www5.pbrc.hawaii.edu\/allen\/"}],"PUBLISHED":["J. Cell Sci. 101:449-461, 1992"],"Contributors":["Richard Allen (University of Hawaii)","C. Schroeder"],"PUBMED":["1629255"]},"BIOLOGICALPROCESS":[{"onto_name":"early endosome to Golgi transport","onto_id":"GO:0034498"},{"onto_name":"clathrin coating of Golgi vesicle, plasma membrane to endosome targeting","onto_id":"GO:0010785"}],"PROCESSINGHISTORY":[{"onto_name":"freeze_fracture\/freeze_etch","onto_id":"FBbi:00000419"},{"onto_name":"shadowing and plating","onto_id":"FBbi:00000398"},{"onto_name":"recorded image","onto_id":"FBbi:00000265"},{"onto_name":"film","onto_id":"FBbi:00000303"},{"onto_name":"unprocessed raw data","onto_id":"FBbi:00000582"}],"PARAMETERIMAGED":[{"onto_name":"elastic scattering of electrons","onto_id":"FBbi:00000586"},{"onto_name":"electron density","onto_id":"FBbi:00000315"},{"onto_name":"elevation","onto_id":"FBbi:00000320"}],"IMAGEDESCRIPTION":{"free_text":"A high resolution of a quick-freeze deep-etch rotary shadowed replica of a parasomal sac from which a clathrin-coated preendosomal vesicle has pinched off. The typical clathrin cage structure is preserved. Fractured trichocyst at the lower left. TEM taken on 6\/7\/88 by C. Schroeder with Zeiss 10A operating at 80kV. Neg. 31,500X. Adapted with permission from the J. Cell Sci. 101:449-461, 1992. The raw film was scanned with an Epson Perfection V750 Pro. This image is best used for quantitative analysis. Additional information available at (http:\/\/www5.pbrc.hawaii.edu\/allen\/)."},"ITEMTYPE":[{"onto_name":"transmission electron microscopy (TEM)","onto_id":"FBbi:00000258"},{"onto_name":"illumination by electrons","onto_id":"FBbi:00000273"}],"CELLULARCOMPONENT":[{"onto_name":"clathrin coat of endocytic vesicle","onto_id":"GO:0030128"},{"onto_name":"early endosome","onto_id":"GO:0005769"},{"onto_name":"integral to endosome membrane","onto_id":"GO:0031303"}],"RELATIONTOINTACTCELL":[{"onto_name":"shadowing and plating","onto_id":"FBbi:00000398"},{"onto_name":"freeze_fracture\/freeze_etch","onto_id":"FBbi:00000419"},{"onto_name":"isolated subcellular component","onto_id":"FBbi:00000579"}],"SOURCEOFCONTRAST":{"onto_name":"differences in deposition of metal shadow","onto_id":"FBbi:00000601"},"GROUP_ID":"5817","DATAQUALIFICATION":{"free_text":"RAW;spatialmeasurements"},"TERMSANDCONDITIONS":{"free_text":"attribution_nc_sa"},"IMAGINGMODE":{"onto_name":"electron density","onto_id":"FBbi:00000315"},"DIMENSION":[{"Space":{"Image_size":3732,"Pixel_size":{"unit":"nanometers","value":0.63},"axis":"X"}},{"Space":{"Image_size":4192,"Pixel_size":{"unit":"nanometers","value":0.63},"axis":"Y"}}],"NCBIORGANISMALCLASSIFICATION":{"onto_name":"Paramecium multimicronucleatum","onto_id":"NCBITaxon:44030"},"PREPARATION":{"onto_name":"freeze_fracture\/freeze_etch","onto_id":"FBbi:00000419"},"VISUALIZATIONMETHODS":{"onto_name":"transmission electron microscopy (TEM)","onto_id":"FBbi:00000258"},"CELLTYPE":[{"onto_name":"cell by organism","onto_id":"CL:0000004"},{"onto_name":"eukaryotic cell","onto_id":"CL:0000255"},{"free_text":"Eukaryotic Protist"},{"free_text":"Ciliated Protist"}]}},"Citation":{"Title":"Richard Allen (University of Hawaii), C. Schroeder (2011) CIL:12633, Paramecium multimicronucleatum, cell by organism, eukaryotic cell, Eukaryotic Protist, Ciliated Protist. CIL. Dataset","ARK":"ark:\/b7295\/w9cil12633","DOI":"doi:10.7295\/W9CIL12633"}}}