NPAP1 产品
(Nuclear Pore Associated Protein 1 (NPAP1))
Categories
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
Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Application
WB, IHC (p), FACS
Validations
- (1)
- (3)
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
Datasheet
Datasheet
Recommended NPAP1 蛋白
Product
Reactivity
Source
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Source
HEK-293 Cells
Validations
- (3)
Cat. No.
ABIN7554784
Quantity
1 mg
Datasheet
Datasheet
Latest Publications for our NPAP1 Products
: "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), C15orf2Protein level used designations for NPAP1
- nuclear pore-associated protein 1
- protein C15orf2
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