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Role for NUP62 depletion and PYK2 (show PTK2B ELISA Kits) redistribution in dendritic retraction resulting from chronic stress
Nup62 depletion leads to the appearance of multinucleated cells and induces the formation of multipolar centrosomes, centriole synthesis defects, dramatic spindle orientation defects, and centrosome component rearrangements that impair cell bi-polarity.
ORP8 (show OSBPL8 ELISA Kits) was shown to compete with Exo70 (show EXOC7 ELISA Kits) for interaction with NUP62, and NUP62 knockdown abolished the migration enhancement of ORP8 (show OSBPL8 ELISA Kits)-silenced cells, suggesting that the endogenous ORP8 (show OSBPL8 ELISA Kits) suppresses migration via binding to NUP62.
Dtaa show that importin beta and the integral nuclear pore glycoprotein Nup62 interact with hsp90, hsp70, p23, and the TPR domain proteins FKBP52 and PP5 during nuclear transport.
it was revealed that a fraction of Nup62 was associated with mitotic spindle microtubule instead of spindle matrix, and the localization of Nup62 in the mitotic spindle depended on its three coiled-coil domains rather than Crm1 (show XPO1 ELISA Kits), although Nup62 strongly interacted with Crm1 (show XPO1 ELISA Kits) during mitosis. Moreover, depletion of Nup62 by small interference of RNA seriously induced the defects of chromosome alignment and spindle assembly
Knockdown of Nup62 (and CaMKK2 (show CAMKK2 ELISA Kits)) reduced androgen receptor (show AR ELISA Kits) transcriptional activity in castrate resistant prostate cancer cells.
The data presented here suggest that BGLF4 interferes with the normal functions of Nup62 and Nup153 (show NUP153 ELISA Kits) and preferentially helps the nuclear import of viral proteins for viral DNA replication and assembly.
These data reveal an emergent Kap (show CDKN3 ELISA Kits)-centric barrier mechanism that may underlie mechanistic and kinetic control in the nuclear pore complex.
Loss of presenilin (PS)1 function propagates tau accumulation through impairment of cargo-receptor protein p62-dependent tau degradation.
A hydrophobic patch 65LRLFV69 within the zinc-binding domain is essential for the nuclear import and localization of HPV8 E7 via hydrophobic interactions with Nup62 and Nup153 (show NUP153 ELISA Kits).
Nup62 and Nup88 protein levels were significantly decreased upon knockdown of O-GlcNAc transferase.
that a patch of hydrophobic residues, 65LRLCV69, within the zinc-binding domain of HPV16 E7 mediates its nuclear import via hydrophobic interactions with the FG domain of the central channel nucleoporin Nup62.
Nucleoporin p62 (NUP62) and nucleoporin 214 (NUP214 (show NUP214 ELISA Kits)) are differentially distributed between nuclear pore complexes.
The nuclear pore complex is a massive structure that extends across the nuclear envelope, forming a gateway that regulates the flow of macromolecules between the nucleus and the cytoplasm. Nucleoporins are the main components of the nuclear pore complex in eukaryotic cells. The protein encoded by this gene is a member of the FG-repeat containing nucleoporins and is localized to the nuclear pore central plug. This protein associates with the importin alpha/beta complex which is involved in the import of proteins containing nuclear localization signals. Multiple transcript variants of this gene encode a single protein isoform.
, nuclear pore glycoprotein p62
, 62 kDa nucleoporin
, nuclear pore glycoprotein 62
, nucleoporin Nup62
, nuclear pore complex 1