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NOL1 encodes a member of the evolutionarily conserved NOL1/NOP2/Sun domain family. Additionally we are shipping Nucleolar Protein 1 Proteins (2) and many more products for this protein.
Showing 10 out of 28 products:
Human Polyclonal NOL1 Primary Antibody for ICC, IF - ABIN4340305
Hong, Lee, Chung: Telomerase activates transcription of cyclin D1 gene through an interaction with NOL1. in Journal of cell science 2016
Show all 2 references for ABIN4340305
results demonstrate that Nop2 is an essential gene for blastocyst formation, and is required for RNA processing and/or stability in vivo during preimplantation embryo development in the mouse.
Findings suggest a newly discovered role of Nop2 in both mature neurons and in cells possibly involved in the regeneration of nervous tissue
Analysis of the Localization of Fibrillarin (show FBL Antibodies) and Sites of Pre-rRNA Synthesis in the Nucleolus-Like Bodies of Mouse GV Oocytes after Mild Treatment with Proteinase K
SUV39h1 (show SUV39H1 Antibodies) associated with HP1 beta (show CBX1 Antibodies) in fibrillarin (show FBL Antibodies)-positive nucleolar regions.
Inappropriate expression of the p120 (show CTNND1 Antibodies) gene can result in aberrant neutrophil maturation.
Results suggest that proteasome-dependent processing of fibrillarin (show FBL Antibodies) occurs upon mercury induction.
This splicing factor (show SLU7 Antibodies) was more abundant in hepatocyte nuclei of mice fed genetically-modified soybeans than in control mice.
massive apoptosis was observed in early Fibrillarin (show FBL Antibodies)(-/-) embryos, showing that fibrillarin (show FBL Antibodies) is essential for development
NOL1 represents a new route by which telomerase activates transcription of cyclin D1 (show CCND1 Antibodies) gene, thus maintaining cell proliferation capacity
p120 (show HNRNPU Antibodies) has an rRNA:5-Methylcytosine-Methyltransferase activity.
Characterization of two novel genes, WBSCR20 (show NSUN5 Antibodies) and WBSCR22 (show WBSCR22 Antibodies), deleted in Williams-Beuren syndrome
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.
nucleolar protein 1
, rRNA 2'-O-methyltransferase fibrillarin
, NOL1/NOP2/Sun domain family, member 1
, NOP2 nucleolar protein homolog
, nucleolar protein 1, 120kDa
, nucleolar protein 2 homolog
, proliferating-cell nucleolar antigen p120
, proliferation-associated nucleolar protein p120
, putative ribosomal RNA methyltransferase NOP2
, nucleolar protein 1, 120 kDa
, NOL1-related protein
, NOL1/NOP2/Sun domain family member 5
, NOP2/Sun domain family, member 5A
, Williams Beuren syndrome chromosome region 20A
, Williams-Beuren syndrome chromosomal region 20A protein
, Williams-Beuren syndrome critical region protein 20 copy A
, putative methyltransferase NSUN5