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NSUN5 anticorps (AA 277-466)

Cet anticorps anti-NSUN5 est un anticorps Lapin Polyclonal détectant NSUN5 dans WB et IHC. Adapté pour Humain.
N° du produit ABIN7268955

Aperçu rapide pour NSUN5 anticorps (AA 277-466) (ABIN7268955)

Antigène

Voir toutes NSUN5 Anticorps
NSUN5 (NOP2/Sun Domain Family, Member 5 (NSUN5))

Reactivité

  • 23
  • 2
  • 1
Humain

Hôte

  • 23
Lapin

Clonalité

  • 23
Polyclonal

Conjugué

  • 6
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp NSUN5 est non-conjugé

Application

  • 20
  • 13
  • 13
  • 9
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Épitope

    • 15
    • 4
    • 1
    • 1
    • 1
    • 1
    AA 277-466

    Fonction

    NSUN5 Rabbit pAb

    Séquence

    SCCELAEEDF LAVSPSDPRY HEVHYILLDP SCSGSGMPSR QLEEPGAGTP SPVRLHALAG FQQRALCHAL TFPSLQRLVY STCSLCQEEN EDVVRDALQQ NPGAFRLAPA LPAWPHRGLS TFPGAEHCLR ASPETTLSSG FFVAVIERVE VPSSASQAKA SAPERTPSPA PKRKKRQQRA AAGACTPPCT

     Réactivité croisée

    Humain, Souris, Rat

    Attributs du produit

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogène

    Recombinant fusion protein containing a sequence corresponding to amino acids 277-466 of human NSUN5 (NP_683759.1).

    Isotype

    IgG
  • Indications d'application

    WB,1:200 - 1:2000,IHC,1:50 - 1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    -20 °C

    Stockage commentaire

    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène

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

    Autre désignation

    NSUN5

    Sujet

    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.,NSUN5,NOL1,NOL1R,NSUN5A,WBSCR20,WBSCR20A,p120,p120(NOL1),Epigenetics & Nuclear Signaling,RNA Binding,Signal Transduction,Endocrine & Metabolism,NSUN5

    Poids moléculaire

    36kDa/42kDa/46kDa/50kDa/51kDa

    ID gène

    55695

    UniProt

    Q96P11
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