Approx 120kDa band observed in lysates of cell lines A431, Daudi and HeLa (calculated MW of 120kDa according to NP_006382.1). An additional band of unknown identity was also consistently observed at 26-28kDa. This band was successfully blocked by incubation with the immunising peptide.
Use a concentration of 1 µg/ml.
Use at an assay dependent concentration. PubMed: 21419860
Functions in nuclear protein import, either by acting as autonomous nuclear transport receptor or as an adapter-like protein in association with the importin-beta subunit KPNB1. Acting autonomously, is thought to serve itself as receptor for nuclear localization signals (NLS) and to promote translocation of import substrates through the nuclear pore complex (NPC) by an energy requiring, Ran-dependent mechanism. At the nucleoplasmic side of the NPC, Ran binds to importin, the importin/substrate complex dissociates and importin is re-exported from the nucleus to the cytoplasm where GTP hydrolysis releases Ran. The directionality of nuclear import is thought to be conferred by an asymmetric distribution of the GTP- and GDP-bound forms of Ran between the cytoplasm and nucleus. Mediates autonomously the nuclear import of ribosomal proteins RPL23A, RPS7 and RPL5. Binds to a beta-like import receptor binding (BIB) domain of RPL23A. In association with KPNB1 mediates the nuclear import of H1 histone and the Ran-binding site of IPO7 is not required but synergizes with that of KPNB1 in importin/substrate complex dissociation. In vitro, mediates nuclear import of H2A, H2B, H3 and H4 histones. In vitro, mediates the nuclear import of HIV-1 reverse transcription complex (RTC) integrase. In case of HIV-1 infection, binds and mediates the nuclear import of HIV-1 Rev.
Belongs to the importin beta family. Contains 1 importin N-terminal domain.
ab15840 stained SW480 cells. The cells were 100% methanol fixed for 5 minutes at room temperature and then incubated in 1%BSA / 0.3M glycine in 0.1% PBS-Tween for 1hour at room temperature to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab15840 at 1µg/ml) overnight at +4°C. The secondary antibody (pseudo-colored green) was ab150133 used at a 1/1000 dilution for 1hour at room temperature. Alexa Fluor® 594 WGA was used to label plasma membranes (pseudo-colored red) at a 1/200 dilution for 1hour at room temperature. DAPI was used to stain the cell nuclei (pseudo-colored blue) at a concentration of 1.43µM for 1hour at room temperature.
Western blot - Anti-Importin 7 antibody (ab15840)
Anti-Importin 7 antibody (ab15840) at 1 µg/ml + Daudi lysate at 35 µg
Predicted band size: 119 kDa Additional bands at: 30 kDa. We are unsure as to the identity of these extra bands.
Detected by chemiluminescence. Please note that an approx 30kDa band of unknown identity is also consistently observed.
Chen J et al. Nuclear Import of Early Growth Response-1 Involves Importin-7 and the Novel Nuclear Localization Signal Serine-Proline-Serine. Int J Biochem Cell Biol : (2011).
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