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NPAP1 产品

(Nuclear Pore Associated Protein 1 (NPAP1))

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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.

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Featured NPAP1 Categories

NPAP1 抗体

High quality antibodies with extensive validation data.

Recommended NPAP1 抗体

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Reactivity
Application
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Datasheet
Reactivity Human
Application WB, IHC (p), FACS
Validations
  • (1)
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Cat. No. ABIN6244208
Quantity 400 μL
Datasheet Datasheet
Reactivity Human
Application IHC, ELISA
Validations
  • (2)
Cat. No. ABIN7238615
Quantity 200 μL
Datasheet Datasheet
Reactivity Human
Application WB, IF (p), IHC (p)
Validations
Cat. No. ABIN1385442
Quantity 100 μL
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Recommended NPAP1 蛋白

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Reactivity
Source
Validations
Cat. No.
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Datasheet
Reactivity Human
Source Tobacco (Nicotiana tabacum)
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  • (1)
Cat. No. ABIN3094224
Quantity 1 mg
Datasheet Datasheet

Latest Publications for our NPAP1 Products

Neumann, Markaki, Mladenov, Hoffmann, Buiting, Horsthemke: "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).

Synonyms and alternative names related to NPAP1

nuclear pore associated protein 1 (NPAP1), C15orf2

Protein level used designations for NPAP1

  • nuclear pore-associated protein 1
  • protein C15orf2
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