NPAP1 Antibodies

AND NPAP1 ELISA kits, NPAP1 Proteins

Many biological assays use antibodies to detect NPAP1, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with NPAP1 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop NPAP1 antibodies...

We validate the specificity of these antibodies to NPAP1 by testing them on tissues known to express NPAP1 positively and negatively. Browse below to find the NPAP1 antibody that suites your experiment. We have 1 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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NPAP1 Infographic by Boster Bio

All NPAP1 Products

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NPAP1 (NM_018958) Human Over-expression Lysate

Human

$960
Cat # LS023742
20 µg, 100 µg

NPAP1 Overview

Facts about Nuclear pore-associated protein 1.

NPAP1 3D structure. Source: alphafold

Nuclear pore-associated protein 1 (NPAP1)

May be involved in spermatogenesis. .

Gene Information

Human
Gene Name:	NPAP1
Uniprot:	Q9NZP6
Entrez:	23742

Family

Belongs to:

No superfamily

Alternative Names

C15orf2; chromosome 15 open reading frame 2; protein C15orf2

Molecular Weight

Mass (kDA):
120.954 kDA

Genomic Context


Human

Location:	15q11.2
Sequence:	15; NC_000015.10 (24675775..24683393)

Subcellular Localizations

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

Diseases

Prader-willi Syndrome

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/NPAP1

References

PMID: 10783265 by Faerber C., et al. Identification of a testis-specific gene (c15orf2) in the Prader- Willi syndrome region on chromosome 15.

PMID: 17337158 by Buiting K., et al. C15orf2 and a novel noncoding transcript from the Prader- Willi/Angelman syndrome region show monoallelic expression in fetal brain.