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Rabbit Anti-NPAP1/FITC Conjugated antibody
background:
This gene is located in the Prader-Willi syndrome region on chromosome 15. This gene is biallelically expressed in adult testis and brain but is paternally imprinted in fetal brain. Defects in this gene may be associated with Prader-Willi syndrome. [provided by RefSeq, Aug 2012]
Function:
May be involved in spermatogenesis.
Subunit:
Associates with the nuclear pore complex (NPC).
Subcellular Location:
Nucleus, nucleoplasm. Nucleus inner membrane. Note=Colocalizes with the NPC and nuclear lamins at the nuclear periphery.
Tissue Specificity:
Testis-specific in adults. In fetal brain expressed only from the paternal allele.
Database links:
Entrez Gene: 23742 Human
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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