NOP2/Sun Domain Family, Member 5 Protéines (NSUN5)

NSUN5 encodes a member of the evolutionarily conserved NOL1/NOP2/Sun domain family. De plus, nous expédions NOP2/Sun Domain Family, Member 5 Anticorps (14) et et beaucoup plus de produits pour cette protéine.

afficher tous les protéines Gène GeneID UniProt
Rat NSUN5 NSUN5 288595  
NSUN5 100609 Q8K4F6
NSUN5 55695 Q96P11
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Top NOP2/Sun Domain Family, Member 5 Protéines sur anticorps-enligne.fr

Showing 4 out of 4 products:

Catalogue No. Origin Source Conjugué Images Quantité Livraison Prix Détails
Cellules d'insectes Humain His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg 60 Days
$9,626.73
Détails
Cellules d'insectes Souris His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg 60 Days
$9,626.73
Détails
Insect cells (Sf9) Humain DYKDDDDK Tag Validation with Western Blot 20 μg 11 Days
$518.10
Détails
Wheat germ Humain GST tag 2 μg 11 to 12 Days
$338.33
Détails

NSUN5 Protéines protéines par origine et source

Origin Exprimée danse Conjugué
Mouse (Murine)

Human , ,
, ,

Plus protéines pour NOP2/Sun Domain Family, Member 5 (NSUN5) partenaires d'interaction

Mouse (Murine) NOP2/Sun Domain Family, Member 5 (NSUN5) interaction partners

  1. The Nsun5 deficiency led to decreases in the number and neurite outgrowth of OPCs in the hippocampal CA1 and DG, with the decline in NG2 expression and OPCs proliferation

  2. mouse homologues of two novel genes, WBSCR20 and WBSCR22, deleted in Williams-Beuren syndrome (WBSCR20; WBSCR22)

Human NOP2/Sun Domain Family, Member 5 (NSUN5) interaction partners

  1. Characterization of two novel genes, WBSCR20 and WBSCR22, deleted in Williams-Beuren syndrome

Profil protéine NOP2/Sun Domain Family, Member 5 (NSUN5)

Profil protéine

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.

Gene names and symbols associated with 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 Protéine
  • AI326939 Protéine
  • NOL1 Protéine
  • NOL1R Protéine
  • NSUN5A Protéine
  • p120 Protéine
  • RGD1309268 Protéine
  • WBSCR20 Protéine
  • WBSCR20A Protéine
  • wu:fc49f12 Protéine
  • zgc:66176 Protéine
  • zgc:77183 Protéine

Protein 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

GENE ID SPECIES
288595 Rattus norvegicus
406690 Danio rerio
463460 Pan troglodytes
479720 Canis lupus familiaris
716219 Macaca mulatta
100194770 Salmo salar
100401569 Callithrix jacchus
100524245 Sus scrofa
100609 Mus musculus
55695 Homo sapiens
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