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The transport of protein and large RNAs through the nuclear pore complexes (NPC) is an energy-dependent and regulated process. Additionally we are shipping and many more products for this protein.
Showing 10 out of 36 products:
Human Polyclonal XPO7 Primary Antibody for ELISA, WB - ABIN185164
Kutay, Hartmann, Treichel, Calado, Carmo-Fonseca, Prehn, Kraft, Gorlich, Bischoff: Identification of two novel RanGTP-binding proteins belonging to the importin beta superfamily. in The Journal of biological chemistry 2001
Knockdown of exportins 4, 5, and 7 altered thyroid hormone receptor (show THRA Antibodies) shuttling dynamics, and when exportins 5 and 7 were overexpressed, TR distribution shifted toward the cytosol.
Human oligodendrogliomas cells stably expressing mutant XPO7 showed altered cell proliferation.
RAN nucleo-cytoplasmic transport and mitotic spindle assembly partners XPO7 and TPX2 (show TPX2 Antibodies) have roles in serous epithelial ovarian cancer
Knockdown of XPO7 reduced the amount of nuclear p65 (show GORASP1 Antibodies) following TNF (show TNF Antibodies) stimulation. XPO7 binding to p65 (show GORASP1 Antibodies) is NLS (show ALDH1A2 Antibodies) independent
These biochemical and functional data reveal RANBP16 and RANBP17 (show RANBP17 Antibodies) as novel regulators of E2A (show TCF3 Antibodies) protein action, and demonstrate specific interaction of E12 (show ELSPBP1 Antibodies) with RANBP17 (show RANBP17 Antibodies).
Exportin 7-dependent nuclear export signals differ fundamentally from the leucine-rich, CRM1 (show XPO1 Antibodies)-dependent ones
STRADalpha facilitates nuclear export of LKB1 (show STK11 Antibodies) by serving as an adaptor between LKB1 (show STK11 Antibodies) and exportins CRM1 (show XPO1 Antibodies) and exportin7.
Knockdown of Xpo7 in primary fetal liver erythroblasts resulted in severe inhibition of chromatin condensation and enucleation but otherwise had little effect on erythroid differentiation, including hemoglobin accumulation.
This study demonstrateg that exportin-7 responds to ischemia in astrocytes.
The transport of protein and large RNAs through the nuclear pore complexes (NPC) is an energy-dependent and regulated process. The import of proteins with a nuclear localization signal (NLS) is accomplished by recognition of one or more clusters of basic amino acids by the importin-alpha/beta complex\; see MIM 600685 and MIM 602738. The small GTPase RAN (MIM 601179) plays a key role in NLS-dependent protein import. RAN-binding protein-16 is a member of the importin-beta superfamily of nuclear transport receptors.
, exportin 7
, RAN binding protein 16
, ran-binding protein 16