Nucleolar Protein 1 抗体
(Nucleolar Protein 1 (NOL1))
This gene encodes a member of the evolutionarily conserved NOL1/NOP2/Sun domain family. The encoded protein may function as a DNA methyltransferase in the nucleus. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2009].
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Latest Publications for our Nucleolar Protein 1 抗体
: "Telomerase activates transcription of cyclin D1 gene through an interaction with NOL1." in: Journal of cell science, Vol. 129, Issue 8, pp. 1566-79, (2016) (PubMed).
: "Probing Functional Changes in Exocyst Configuration with Monoclonal Antibodies." in: Frontiers in cell and developmental biology, Vol. 4, pp. 51, (2016) (PubMed).
: "Probing Functional Changes in Exocyst Configuration with Monoclonal Antibodies." in: Frontiers in cell and developmental biology, Vol. 4, pp. 51, (2016) (PubMed).
Aliases for Nucleolar Protein 1 抗体
NOP2 nucleolar protein (Nop2) 抗体NOP2 nucleolar protein (NOP2) 抗体
NOP2 nucleolar protein homolog (yeast) (nop2) 抗体
120kDa 抗体
A530002O17 抗体
cb164 抗体
im:6893299 抗体
Nol1 抗体
NOL1 抗体
NOP120 抗体
NSUN1 抗体
p120 抗体
sb:cb164 抗体
si:dkey-91i17.1 抗体
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