Consensus outcome revealed that 98.71% OsMYB and all AtMYB proteins were found to be nuclear localized and confirmed by the presence of nuclear localization signal (NLS).
Unexpectedly, all eEF1H subunits were found to be present in both cytoplasmic and nuclear fractions of A549 cells which contradicted the data on the cancer tissues where eEF1A and eEF1Bα were not found in nucleus.
Nucleoplasmin, a nuclear protein implicated in ribosomal export, was found to be bound to some miRNAs but not all [ 30].
EZH2, H3K27me3, H2A.Z and nuclear longPolyA, reflecting nuclear transcription levels, were found to be significantly different between subjects and escapes across all three examined genomic sections.
They were all found to direct nuclear export in a Leptomycin B sensitive manner, suggesting that the reverse peptides function as active NESs in cells.
PBX3, PU1, POL2, YY1, and nuclear factor κB have all been found to bind here in ENCODE ChIP-seq experiments.
We found endogenous LAMR to be both cytosolic and nuclear in all cell lines.
Moreover, they found a translocation of S100A11 expression from exclusively nuclear location in normal tissues to cytoplasmic and nuclear in all common cancers.
The important DNA damage signaling protein, namely, PARP-1, is most abundantly found nuclear protein almost in all eukaryotes other than yeast.
FABP7 expression can be found in all grades of astrocytoma, but neoplastic cells with nuclear FABP7 were only seen in infiltrative types of tumors.
