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Description
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
Specifications
Specifications
| Antigen | necdin homolog (mouse) |
| Applications | ELISA, Western Blot |
| Classification | Monoclonal |
| Clone | 2D11 |
| Conjugate | Unconjugated |
| Description | Mouse monoclonal antibody raised against a partial recombinant NDN. |
| Formulation | PBS with no preservative; pH 7.4 |
| Gene | NDN |
| Gene Accession No. | NM_002487 |
| Gene Alias | HsT16328/PWCR |
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