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Invitrogen™ Human NSUN5 (aa 133-210) Control Fragment Recombinant Protein
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Quantity:
100 μL
Unit Size:
100µL
Description
Highest antigen sequence indentity to the following orthologs: Mouse (88%), Rat (88%). This recombinant protein control fragment may be used for blocking experiments with the corresponding antibody, PA5-54228 (PA5-54228. In IHC/ICC and WB experiments, we recommend a 100x molar excess of the protein fragment control based on the concentration and the molecular weight. Pre-incubate the antibody-protein control fragment mixture for 30 min at room temperature.
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
Specifications
| Accession Number | Q96P11 |
| Concentration | ≥5.0 mg/mL |
| For Use With (Application) | Blocking Assay, Control |
| Formulation | 1 M urea, PBS with no preservative; pH 7.4 |
| Gene ID (Entrez) | 55695 |
| Name | Human NSUN5 (aa 133-210) Control Fragment |
| Quantity | 100 μL |
| Regulatory Status | RUO |
| Gene Alias | 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 5 A; NOP2/Sun RNA methyltransferase family member 5; Nsun5; NSUN5A; p120; p120(NOL1); Probable 28 S rRNA (cytosine-C(5))-methyltransferase; putative methyltransferase NSUN5; RGD1309268; WBSCR20; Wbscr20a; Williams Beuren syndrome chromosome region 20 A; Williams Beuren syndrome chromosome region 20 A homolog; Williams-Beuren syndrome chromosomal region 20 A protein; Williams-Beuren syndrome chromosomal region 20 A protein homolog; Williams-Beuren syndrome critical region protein 20; Williams-Beuren syndrome critical region protein 20 copy A |
| Common Name | NSUN5 |
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