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NDN
Necdin, MAGE family memberHsT16328, PWCR
This intronless gene is located in the Prader-Willi syndrome deletion region. It is an imprinted gene and is expressed exclusively from the paternal allele. Studies in mouse suggest that the protein encoded by this gene may suppress growth in postmitotic neurons. [provided by RefSeq, Jul 2008]
Top validated antibodies |
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| Novus Biologicals |  H00004692-M02 |
2 references | Monoclonal |
WB
EL
ICC
IHC
BN
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| antibodies-online | ABIN393245 |
5 references | Monoclonal |
WB
EL
ICC
IHC
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| Abnova Corporation | H00004692-M02 |
1 references | Monoclonal |
WB
EL
ICC
IHC
|
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| OriGene | AM31803PU-N |
Monoclonal |
WB
EL
ICC
IHC
|
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| Acris Antibodies GmbH | AM31803PU-N |
Monoclonal |
WB
EL
ICC
IHC
|
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