A5992
NSUN5 Rabbit polyclonal antibody
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£152.00
- SKU:
- A5992
- Zusätzliche Namen:
- NOL1|NOL1R|NSUN5|NSUN5A|p120|p120(NOL1)|WBSCR20|WBSCR20A
- Anwendung:
- ELISA, WB, IHC-P
- Molekulargewicht:
- 47kda
- Spezies-Reaktivität:
- Human
- Aufreinigung:
- Affinity Purified
- Lagerbedingungen:
- -20[o]C Avoid freeze/thaw cycles.
- Hersteller:
- Abclonal
- Host:
- Rabbit
- Reaktivitäten:
- Human, Mouse, Rat
- Immunogen:
- Recombinant protein (or fragment).This information is considered to be commercially sensitive.
- Formulierung:
- Unmodified
- Sequenz:
- RPGPASQLPRFVRVNTLKTCSDDVVDYFKRQGFSYQGRASSLDDLRALKGKHFLLDPLMPELLVFPAQTDLHEHPLYRAGHLILQDRASCLPAMLLDPPPGSHVIDACAAPGNKTSHLAALLKNQGKIFAFDLDAKRLASMATLLARAGVSCCELAEEDFLAVSPSDPRYHEVHYILLDPSCSGSGMPSRQLEEPGAGTPSPVRLHALAGFQQRALCHALTFPSLQRLVYSTCSLCQEENEDVVRDALQQNPGAFRLAPALPAWPHRGLSTFPGAEHCLRASPETTLSSGFFVAVIERVEVPR
- Uniprot:
- Q96P11
- Synonyme:
- 28S rRNA (cytosine-C(5))-methyltransferase;NOL1;NOL1-related protein;NOL1/NOP2/Sun domain family member 5;NOL1R;NOP2/Sun domain family, member 5;NOP2/Sun domain family, member 5A;NOP2/Sun RNA methyltransferase family member 5;NSUN5A;p120;p120(NOL1);probable 28S rRNA (cytosine-C(5))-methyltransferase;putative methyltransferase NSUN5;WBSCR20;WBSCR20A;Williams Beuren syndrome chromosome region 20A;Williams-Beuren syndrome chromosomal region 20A protein;Williams-Beuren syndrome critical region protein 20 copy A
- Weitere Details:
- This gene encodes a member of an evolutionarily conserved family of proteins that may function as methyltransferases. This gene is located in a larger region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. There are two pseudogenes for this gene located in the same region of chromosome 7. Alternative splicing results in multiple transcript variants encoding different isoforms.
- Versandbedingungen:
- Blue Ice