{"database":"bioimages","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"submitter":["Naoki Tamura"],"journal":["The Journal of Cell Biology"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-JCBD-201302067"],"attach_to":["JCB"],"legend":["PpAtg18-YFP-expressing strain was shifted from synthetic dextrose medium to H<sub>2</sub>O.<br /><br />Red: Vacuole stained with FM 4-64, Green: PpAtg18-YFP, Blue: DIC. <br />","Wild-type PpAtg18-YFP-expressing strain was shifted from synthetic methanol medium to synthetic dextrose medium to induce micropexophagy.<br /> Red: Vacuole stained with FM 4-64, Green: PpAtg18-YFP, Blue: DIC. <br />","Wild-type PpAtg18-YFP-expressing strain was grown on synthetic methanol medium prior to induction of pexophagy. Red: Vacuole stained with FM 4-64, Green: PpAtg18-YFP, Blue: DIC. <br /><br />","PpAtg18-YFP-expressing strain was shifted from synthetic dextrose medium to synthetic dextrose medium.<br />Red: Vacuole stained with FM 4-64, Green: PpAtg18-YFP, Blue: DIC.  <br />","YFP-tagged PpAtg18 DD mutant was expressed.  Cells were shifted from synthetic methanol medium to synthetic dextrose medium to induce micropexophagy.  <br />Red: Vacuole stained with FM 4-64, Green: PpAtg18 DD-YFP, Blue: DIC.<br />","PpAtg18-YFP-expressing strain was shifted from synthetic dextrose medium to synthetic dextrose + 0.9 M NaCl medium.<br />Red: Vacuole stained with FM 4-64, Green: PpAtg18-YFP, Blue: DIC.  <br />","PpAtg18-YFP-expressing strain was shifted from synthetic dextrose medium to synthetic methanol (YNB + 0.8% methanol) medium.<br />Red: Vacuole stained with FM 4-64, Green: PpAtg18-YFP, Blue: DIC.  <br />","PpAtg18-YFP-expressing strain was shifted from synthetic dextrose medium to YNB + 20% glucose medium.<br /><br />Red: Vacuole stained with FM 4-64, Green: PpAtg18-YFP, Blue: DIC.","Wild-type PpAtg18-YFP-expressing strain was shifted from synthetic methanol medium to synthetic ethanol (YNB + 0.8% ethanol) medium to induce macropexophagy.<br /> Red: Vacuole stained with FM 4-64, Green: PpAtg18-YFP, Blue: DIC.","PpAtg18-YFP-expressing fab1∆ strain was shifted from synthetic methanol medium to synthetic dextrose medium to induce micropexophagy.<br />fab1∆<br />","PpAtg18-YFP-expressing strain was shifted from synthetic dextrose  (YNB + glucose) medium to YNB medium without glucose.<br />Red: Vacuole stained with FM 4-64, Green: PpAtg18-YFP, Blue: DIC.  <br />","YFP-tagged PpAtg18 AA mutant was expressed.  Cells were shifted from synthetic methanol medium to synthetic dextrose medium to induce micropexophagy.  <br />Red: Vacuole stained with FM 4-64, Green: PpAtg18 AA-YFP, Blue: DIC.<br />"],"repository":["bioimages"],"figure_sub":["Image 291985 (Figure 6 - C)","Image 291982 (Figure 4 - B)","Image 291987 (Figure 6 - E)","Image 291980 (Figure 4 - B)","Image 291983 (Figure 6 - C)","Image 291978 (Figure 4 - B)","Figure 4","Figure 4 - B","Image 291984 (Figure 6 - C)","Figure 6","Figure 6 - C","Image 291981 (Figure 4 - B)","Image 291986 (Figure 6 - C)","Image 291988 (Figure 6 - E)","Image 291977 (Figure 4 - B)","Figure 6 - E","Image 291979 (Figure 4 - B)"],"pubmed_authors":["Masahide Oku","Naoki Tamura","Fuyuhiko Inagaki","Yasuyoshi Sakai","Moemi Ito","Nobuo N. Noda"],"additional_accession":[]},"is_claimable":false,"name":"Atg18 phosphoregulation controls organellar dynamics by modulating its phosphoinositide-binding activity","description":null,"dates":{"release":"2013-08-12T11:24:45Z","modification":"2018-11-29T11:24:45Z","creation":"2018-11-29T11:24:45Z"},"accession":"S-JCBD-201302067","cross_references":{"doi":["10.1083/jcb.201302067"]}}