About   Help   FAQ
Gene Expression Data
Assay Details
Assay
Reference: J:223046 Rieusset A, et al., Stochastic loss of silencing of the imprinted Ndn/NDN allele, in a mouse model and humans with prader-willi syndrome, has functional consequences. PLoS Genet. 2013;9(9):e1003752
Assay type: Western blot
MGI Accession ID: MGI:6450153
Gene symbol: Ndn
Gene name: necdin, MAGE family member
Antibody: anti-Necdin
Detection system: Secondary antibody coupled to horseradish peroxidase
Results
Image: S1A ©

 Sample Information Bands Other Sample Information
Lane AgeStructure 37 kDa Genetic BackgroundMutant Allele(s)Sex Note
WT P1 TS27: brain Present C57BL/6J Not Specified
Ndn+m/-p P1 TS27: brain Weak (a) involves: 129S2/SvPas * C57BL/6J Ndntm1.1Mus/Ndn+Not Specified Maternally derived allele.
Ndn+m/-p P1 TS27: brain Weak (a) involves: 129S2/SvPas * C57BL/6J Ndntm1.1Mus/Ndn+Not Specified Maternally derived allele.
Ndn+m/-p P1 TS27: brain Absent involves: 129S2/SvPas * C57BL/6J Ndntm1.1Mus/Ndn+Not Specified Maternally derived allele.
Ndn+m/-p P1 TS27: brain Absent involves: 129S2/SvPas * C57BL/6J Ndntm1.1Mus/Ndn+Not Specified Maternally derived allele.
-/- P1 TS27: brain Absent B6.129S2-Ndntm1.1Mus Ndntm1.1Mus/Ndntm1.1MusNot Specified
Notes:
(a) Four out of eight mice exhibited a faint signal (10-20-fold less intense compared to WT).
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
03/25/2025
MGI 6.24 		The Jackson Laboratory