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Gene Expression Data
Assay Details
Assay
Reference: J:59407 Maw MA, et al., A frameshift mutation in prominin (mouse)-like 1 causes human retinal degeneration. Hum Mol Genet. 2000 Jan 1;9(1):27-34
Assay type: Immunohistochemistry
MGI Accession ID: MGI:5644463
Gene symbol: Prom1
Gene name: prominin 1
Antibody: mAb 13A4
Detection system: Secondary antibody coupled to colloidal gold
Results
Specimen 5a: postnatal adult (more )
Structure Level Pattern Image Note
TS28: photoreceptor layer outer segment Present Regionally restricted 5a Expression was highest over the membrane evaginations (17.4 fold hogher). The more distal region of the rod outer segment containing the disks was sparsely labeled.
Specimen 5b: postnatal adult (more )
Structure Level Pattern Image Note
TS28: photoreceptor layer outer segment Present Regionally restricted 5b Expression was highest over the membrane evaginations (17.4 fold hogher). The more distal region of the rod outer segment containing the disks was sparsely labeled.
Specimen 5c: postnatal adult (more )
Structure Level Pattern Image Note
TS28: photoreceptor layer outer segment Present Regionally restricted 5c Expression was highest over the membrane evaginations (17.4 fold hogher). The more distal region of the rod outer segment containing the disks was sparsely labeled.
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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04/16/2024
MGI 6.23 		The Jackson Laboratory