渲染靶标:SSR
Render Timestamp: 2025-03-11T12:18:36.530Z
Commit: cb76efb1e1bf27d454180ac9a5e8c179c097b4c4
XML generation date: 2024-04-05 20:46:28.262
Product last modified at: 2025-02-06T12:30:13.109Z
1% for the Planet 标识
PDP - Template Name: Polyclonal Antibody
PDP - Template ID: *******59c6464

NUP62 Antibody #86980

Filter:
  • WB
  • IP
Western Blotting Image 1: NUP62 Antibody
Western blot analysis of extracts from various cell lines using NUP62 Antibody.

To Purchase # 86980

Supporting Data

REACTIVITY H
SENSITIVITY Endogenous
MW (kDa) 62
SOURCE Rabbit
Application Key:
  • WB-Western Blotting 
  • IP-Immunoprecipitation 
Species Cross-Reactivity Key:
  • H-Human 
  • Related Products

Product Information

Product Usage Information

Application Dilution
Western Blotting 1:1000
Immunoprecipitation 1:50

Storage

Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/ml BSA and 50% glycerol. Store at –20°C. Do not aliquot the antibody.

Protocol

Specificity / Sensitivity

NUP62 Antibody recognizes endogenous levels of total NUP62 protein.

Species Reactivity:

Human

Source / Purification

Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Gly170 of human NUP62 protein. Antibodies are purified by peptide affinity chromatography.

Background

The nuclear pore complex (NPC) is a multi-subunit protein channel that spans the nuclear envelope and is responsible for the nucleocytoplasmic trafficking of RNA, proteins, and ribonucleoproteins (1,2). Nucleoporin p62 (NUP62) is a ubiquitously-expressed 62 kDa protein that is an essential component of the NPC (3). NUP62 expression is increased in aggressive, lethal prostate cancer, and knockdown of NUP62 expression reduces cancer cell proliferation and colony formation in soft agar (4). NUP62 is also highly expressed in squamous cell carcinomas (SCCs), and depletion of NUP62 in SCC cells results in reduced proliferation and enhanced differentiation via regulation of p63 nucleo-cytoplasmic transport (5). Interestingly, NUP62 also plays a role in mitotic cell cycle progression after disassembly of the nuclear envelope and NPCs. Indeed, knockdown of NUP62 induces G2/M phase arrest, mitotic cell death, and abnormal centrosome assembly (6). A missense mutation of Q391P in NUP62 is believed to cause infantile bilateral striatal necrosis (IBSN), a rare and fatal autosomal recessive disease (7).
For Research Use Only. Not For Use In Diagnostic Procedures.
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