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Invitrogen™ NSUN5 Polyclonal Antibody

Rabbit Polyclonal Antibody

Supplier:  Invitrogen™ PA583781

Catalog No. PIPA583781


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Description

Description

Immunogen sequence: MPSRQLEDPG AGTPSPVRLH ALAGFQQRAL CHALTFPSLQ RL.

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.
TRUSTED_SUSTAINABILITY
Specifications

Specifications

NSUN5
Polyclonal
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
Antigen Affinity Chromatography
RUO
55695
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Liquid
Immunocytochemistry, Immunofluorescence
0.05 mg/mL
PBS with 40% glycerol and 0.02% sodium azide; pH 7.2
Q96P11
Nsun5
Recombinant protein corresponding to Human NSUN5.
100 μL
Primary
Human
Antibody
IgG
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