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NSUN5 Rabbit anti-Human, Mouse, Rat, Polyclonal, Proteintech
Rabbit Polyclonal Antibody
Supplier: Proteintech Group Inc 154491AP150UL
Description
NSUN5 is a member of the evolutionarily conserved NOL1/NOP2/Sun domain family. The encoded protein may function as a DNA methyltransferase in the nucleus. The 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.Specifications
| NSUN5 | |
| Polyclonal | |
| Unconjugated | |
| NSUN5 | |
| NOL1, NOL1 related protein, NOL1R, NSUN5, NSUN5A, p120, WBSCR20, WBSCR20A, Ynl022cL | |
| Rabbit | |
| Antigen Affinity Chromatography | |
| RUO | |
| 100609, 288595, 55695 | |
| -20°C | |
| Liquid |
| Immunocytochemistry, Immunofluorescence, Immunohistochemistry (Paraffin), Western Blot | |
| 0.21 mg/mL | |
| PBS with 50% glycerol and 0.02% sodium azide; pH 7.3 | |
| Q8K4F6, Q96P11 | |
| Nsun5 | |
| NSUN5 Fusion Protein Ag7711 | |
| 150 μL | |
| Primary | |
| Human, Mouse, Rat | |
| Antibody | |
| IgG |
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