NPAP1 抗体
(Nuclear Pore Associated Protein 1 (NPAP1))
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.
| Catalog no. | 产品 | 适用 | 宿主 / 克隆类型 | 应用 | 价格和交货时间 |
|---|---|---|---|---|---|
| NPAP1 抗体 (Alexa Fluor 647) | 人 | 兔 Polyclonal |
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| NPAP1 抗体 (Alexa Fluor 594) | 人 | 兔 Polyclonal |
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| NPAP1 抗体 (Alexa Fluor 488) | 人 | 兔 Polyclonal |
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| NPAP1 抗体 | 人 | 兔 Polyclonal |
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Latest Publications for our NPAP1 抗体
: "The imprinted NPAP1/C15orf2 gene in the Prader-Willi syndrome region encodes a nuclear pore complex associated protein." in: Human molecular genetics, Vol. 21, Issue 18, pp. 4038-48, (2013) (PubMed).
Aliases for NPAP1 抗体
nuclear pore associated protein 1 (NPAP1) 抗体C15orf2 抗体
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