NPAP1 rabbit pAb

Sizes: 50μL, 100μL

Catalogue Numbers: ES14464-50, ES14464-100

Citations, Manuals and MSDS Available upon request.

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],

Source: Rabbit

Applications: WB

Dilution: WB 1: 500-2000

Reactivity: Human; Rat; Mouse;

Immunogen: Synthesized peptide derived from human NPAP1 AA range: 960-1010

Storage and Stability: -20°C/1 year

Clonality: Polyclonal

Isotype: IgG

Concentration: 1 mg/ml

Human Gene ID: 23742

Human SWISS Prot NO: Q9NZP6

Subcellular Location: Nucleus, nucleoplasm. Nucleus inner membrane. Colocalizes with the NPC and nuclear lamins at the nuclear periphery.

Research Use Only