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Invitrogen™ NSUN5 Recombinant Rabbit Monoclonal Antibody (PSH05-07)

Rabbit Recombinant Monoclonal Antibody
Brand: Invitrogen™ MA556490
This item is not returnable.
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Description
NSUN5 Recombinant Monoclonal Antibody for Western Blot
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 | |
| Recombinant Monoclonal | |
| 1 mg/mL | |
| PBS with 0.1% BSA, 40% glycerol and 0.05% sodium azide; pH 7.4 | |
| Q8K4F6, Q96P11 | |
| Nsun5 | |
| Synthetic peptide within human NSUN5 aa 51-100/429. | |
| 100 μL | |
| Primary | |
| Human, Mouse, Rat | |
| Antibody | |
| IgG |
| Western Blot | |
| PSH05-07 | |
| Unconjugated | |
| Nsun5 | |
| 9830109N13Rik; AI326939; FLJ10267; MGC986; NOL1; NOL1/NOP2/Sun domain family member 5; NOL1/NOP2/Sun domain family, member 5; NOL1R; NOL1-related protein; NOP2/Sun domain family, member 5; NOP2/Sun domain family, member 5A; NOP2/Sun RNA methyltransferase family member 5; Nsun5; NSUN5A; p120; p120(NOL1); Probable 28S rRNA (cytosine-C(5))-methyltransferase; putative methyltransferase NSUN5; RGD1309268; WBSCR20; Wbscr20a; Williams Beuren syndrome chromosome region 20A; Williams Beuren syndrome chromosome region 20A homolog; Williams-Beuren syndrome chromosomal region 20A protein; Williams-Beuren syndrome chromosomal region 20A protein homolog; Williams-Beuren syndrome critical region protein 20; Williams-Beuren syndrome critical region protein 20 copy A | |
| Rabbit | |
| Protein A | |
| RUO | |
| 100609, 288595, 55695 | |
| Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. | |
| Liquid |
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