R Recombinant
Recombinant: Superior lot-to-lot consistency, continuous supply, and animal-free manufacturing.
NUP62 (E4Y5P) Rabbit mAb #24588
Filter:
- WB
- IF
Supporting Data
REACTIVITY | H |
SENSITIVITY | Endogenous |
MW (kDa) | 62 |
Source/Isotype | Rabbit IgG |
Application Key:
- WB-Western Blotting
- IF-Immunofluorescence
Species Cross-Reactivity Key:
- H-Human
Product Information
Product Usage Information
Application | Dilution |
---|---|
Western Blotting | 1:1000 |
Immunofluorescence (Immunocytochemistry) | 1:100 - 1:400 |
Storage
Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/mL BSA, 50% glycerol, and less than 0.02% sodium azide. Store at –20°C. Do not aliquot the antibody.
Protocol
Specificity / Sensitivity
NUP62 (E4Y5P) Rabbit mAb recognizes endogenous levels of total NUP62 protein.
Species Reactivity:
Human
Source / Purification
Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Gly170 of human NUP62 protein.
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).
- Raices, M. and D'Angelo, M.A. (2017) Curr Opin Cell Biol 46, 26-32.
- Xu, S. and Powers, M.A. (2009) Semin Cell Dev Biol 20, 620-30.
- Carmo-Fonseca, M. et al. (1991) Eur J Cell Biol 55, 17-30.
- Rodriguez-Bravo, V. et al. (2018) Cell 174, 1200-1215.e20.
- Hazawa, M. et al. (2018) EMBO Rep 19, 73-88.
- Hashizume, C. et al. (2013) Cell Cycle 12, 3804-16.
- Basel-Vanagaite, L. et al. (2006) Ann Neurol 60, 214-22.
限制使用
除非 CST 的合法授书代表以书面形式书行明确同意,否书以下条款适用于 CST、其关书方或分书商提供的书品。 任何书充本条款或与本条款不同的客书条款和条件,除非书 CST 的合法授书代表以书面形式书独接受, 否书均被拒书,并且无效。
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For Research Use Only. Not For Use In Diagnostic Procedures.
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