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Gene Expression Data
Assay Details
Assay
Reference: J:253968 Abdelhamed Z, et al., A mutation in Ccdc39 causes neonatal hydrocephalus with abnormal motile cilia development in mice. Development. 2018 Jan 9;145(1):dev154500
Assay type: Immunohistochemistry
MGI Accession ID: MGI:6147583
Gene symbol: Foxj1
Gene name: forkhead box J1
Antibody: anti-Foxj1
Detection system: Secondary antibody coupled to Alexa Fluor 568
Results
Specimen 4G E16.5 FOXJ1: embryonic day 16.5 (more )
Note: Triple labeled: red - Foxj1; green - Ccdc39 (assay MGI:6147580); blue - DAPI.
Structure Level Pattern Image Note
TS24: brain ventricle Present Regionally restricted 4G E16.5 , 4G E16.5 merged , 4G E16.5 FOXJ1 Co-expression with Ccdc39 in ependhymal cells on ventromedial walls as early as E16.
Specimen 4G P0 FOXJ1: postnatal day 0 (more )
Note: Triple labeled: red - Foxj1; green - Ccdc39 (assay MGI:6147580); blue - DAPI.
Structure Level Pattern Image Note
TS27: ependyma Present Regionally restricted 4G P0 , 4G P0 merged , 4G P0 FOXJ1 Co-expression with Ccdc39 in ependhymal cells on ventromedial walls continues through P0.
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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04/30/2024
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