NSUN5 Rabbit anti-Human, Polyclonal, Bioss

Rabbit Polyclonal Antibody

Supplier:  Bioss BS19480R

Catalog No. 50-198-9875

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

• Antigen: NSUN5
• Classification: Polyclonal
• Conjugate: Unconjugated
• Gene: Nsun5
• 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 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
• Host Species: Rabbit
• Purification Method: Protein A
• Regulatory Status: RUO
• Gene ID (Entrez): 55695
• Content And Storage: -20°C
• Form: Liquid

• Applications: Western Blot
• Concentration: 1 μg/mL
• Formulation: TBS with 1% BSA, 50% glycerol and 0.03% Proclin 300; pH
• Gene Accession No.: Q96P11
• Gene Symbols: Nsun5
• Immunogen: KLH conjugated synthetic peptide derived from human NSUN5.
• Quantity: 100 μL
• Primary or Secondary: Primary
• Target Species: Human
• Product Type: Antibody
• Isotype: IgG