NSUN5 产品
(NOP2/Sun Domain Family, Member 5 (NSUN5))
Categories
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. [provided by RefSeq, Dec 2009].
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Featured NSUN5 Categories
Recommended NSUN5 抗体
Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Application
WB, IHC
Validations
- (5)
Cat. No.
ABIN7268955
Quantity
100 μL
Datasheet
Datasheet
Reactivity
Human
Application
WB, ELISA, IF (cc), IF (p), IHC (fro), IHC (p), ICC
Validations
- (1)
Cat. No.
ABIN5675698
Quantity
100 μL
Datasheet
Datasheet
Reactivity
Human
Application
WB, ELISA
Validations
- (1)
Cat. No.
ABIN7164319
Quantity
100 μg
Datasheet
Datasheet
Recommended NSUN5 ELISA试剂盒
Product
Reactivity
Analytical Method
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Analytical Method
Quantitative Sandwich ELISA
Validations
Cat. No.
ABIN6234302
Quantity
96 tests
Datasheet
Datasheet
Recommended NSUN5 蛋白
Synonyms and alternative names related to NSUN5
NOP2/Sun RNA methyltransferase family member 5 (Nsun5), NOP2/Sun domain family, member 5 (nsun5), NOP2/Sun RNA methyltransferase family member 5 (NSUN5), NOP2/Sun RNA methyltransferase family member 5 (nsun5), NOL1/NOP2/Sun domain family, member 5 (Nsun5), 9830109N13Rik, AI326939, NOL1, Nol1r, NOL1R, NSUN5A, p120, RGD1309268, Wbscr20, WBSCR20, Wbscr20a, WBSCR20A, wu:fc49f12, zgc:66176, zgc:77183Protein level used designations for NSUN5
- NOL1/NOP2/Sun domain family, member 5
- NOP2/Sun domain family, member 5
- methyltransferase NSUN5
- putative methyltransferase NSUN5-like
- Williams Beuren syndrome chromosome region 20A homolog
- Williams-Beuren syndrome critical region protein 20
- putative methyltransferase NSUN5
- williams-Beuren syndrome chromosomal region 20A protein homolog
- NOL1-related protein
- NOL1/NOP2/Sun domain family member 5
- NOP2/Sun domain family, member 5A
- Williams Beuren syndrome chromosome region 20A
- Williams-Beuren syndrome chromosomal region 20A protein
- Williams-Beuren syndrome critical region protein 20 copy A
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