{"CIL_CCDB":{"Status":{"Is_public":true,"Deleted":false,"Publish_time":1303185600},"Data_type":{"Still_image":true,"Z_stack":false,"Video":false,"Time_series":false},"CIL":{"Image_files":[{"File_type":"OME_tif","File_path":"12639.tif","Size":34400000,"Mime_type":"image\/tif"},{"File_type":"Zip","File_path":"12639.zip","Size":34314082,"Mime_type":"application\/zip"},{"File_type":"Jpeg","File_path":"12639.jpg","Size":5600854,"Mime_type":"image\/jpeg; charset=utf-8"}],"CORE":{"ATTRIBUTION":{"URLs":[{"Href":"http:\/\/www5.pbrc.hawaii.edu\/allen\/"}],"PUBLISHED":["J. Cell Sci. 101:449-461, 1992"],"Contributors":["Richard Allen (University of Hawaii)"],"PUBMED":["1629255"]},"BIOLOGICALPROCESS":[{"onto_name":"cytoplasm organization","onto_id":"GO:0007028"},{"onto_name":"endosome organization","onto_id":"GO:0007032"},{"onto_name":"clathrin coat assembly","onto_id":"GO:0048268"},{"onto_name":"microtubule basal body organization","onto_id":"GO:0032053"}],"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":"High resolution view of an early endosome with at least two coated evaginations showing, lies next to the proximal end of a fractured basal body. Other clathrin cages may indicate other evaginations from the same early endosome or from another nearby early endosome. TEM taken on 6\/6\/91 by R. Allen with Zeiss 10A operating at 80kV. Neg. 31,500X. Adapted with permission from J. Cell Sci. 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":"cytoplasm","onto_id":"GO:0005737"},{"onto_name":"cell cortex","onto_id":"GO:0005938"},{"onto_name":"endosome membrane","onto_id":"GO:0010008"},{"onto_name":"clathrin coat","onto_id":"GO:0030118"},{"onto_name":"microtubule basal body","onto_id":"GO:0005932"}],"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":"7159","DATAQUALIFICATION":{"free_text":"RAW;spatialmeasurements"},"TERMSANDCONDITIONS":{"free_text":"public_domain"},"IMAGINGMODE":{"onto_name":"electron density","onto_id":"FBbi:00000315"},"DIMENSION":[{"Space":{"Image_size":4310,"Pixel_size":{"unit":"nanometers","value":0.63},"axis":"X"}},{"Space":{"Image_size":3980,"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) (2011) CIL:12639, Paramecium multimicronucleatum, cell by organism, eukaryotic cell, Eukaryotic Protist, Ciliated Protist. CIL. Dataset","ARK":"ark:\/b7295\/w9cil12639","DOI":"doi:10.7295\/W9CIL12639"}}}