NOP2/Sun Domain Family, Member 5 (NSUN5) (C-Term) Peptide
NSUN5
Reactivité: Humain
Hôte: Synthetic
BP, WB
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- Antigène Tous les produits NSUN5
- NSUN5 (NOP2/Sun Domain Family, Member 5 (NSUN5))
- Protein Region
- C-Term
- Origine
- Humain
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB)
- Séquence
- ASPETTLSSG FFVAVIERVE VPSSASQAKA SAPERTPSPA PKRKKRQQRA
- Attributs du produit
- This is a synthetic peptide designed for use in combination with anti-NSUN5 Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
- Purification
- Purified
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- Indications d'application
- Each Investigator should determine their own optimal working dilution for specific applications.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Concentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Conseil sur la manipulation
- Avoid repeated freeze-thaw cycles.
- Stock
- -20 °C
- Stockage commentaire
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Antigène
- NSUN5 (NOP2/Sun Domain Family, Member 5 (NSUN5))
- Synonymes
- RGD1309268 Peptide, wu:fc49f12 Peptide, zgc:66176 Peptide, zgc:77183 Peptide, 9830109N13Rik Peptide, AI326939 Peptide, Nol1r Peptide, Wbscr20 Peptide, Wbscr20a Peptide, NOL1 Peptide, NOL1R Peptide, NSUN5A Peptide, WBSCR20 Peptide, WBSCR20A Peptide, p120 Peptide, NOP2/Sun RNA methyltransferase family member 5 Peptide, NOP2/Sun domain family, member 5 Peptide, NOL1/NOP2/Sun domain family, member 5 Peptide, Nsun5 Peptide, nsun5 Peptide, NSUN5 Peptide
- Sujet
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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.
Alias Symbols: FLJ10267, MGC986, NOL1, NOL1R, NSUN5A, WBSCR20, WBSCR20A, p120
Protein Size: 466 - Poids moléculaire
- 50 kDa
- ID gène
- 55695
- NCBI Accession
- NM_148956, NP_683759
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