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PABPN1 anticorps

Cet anticorps Lapin Monoclonal détecte spécifiquement PABPN1 dans WB, IF et IHC. Il présente une réactivité envers Humain.
N° du produit ABIN7269445

Aperçu rapide pour PABPN1 anticorps (ABIN7269445)

Antigène

Voir toutes PABPN1 Anticorps
PABPN1 (Poly A Binding Protein Nuclear 1 (PABPN1))

Reactivité

  • 30
  • 14
  • 4
  • 4
  • 3
  • 3
  • 3
  • 3
  • 1
Humain

Hôte

  • 30
Lapin

Clonalité

  • 19
  • 11
Monoclonal

Conjugué

  • 18
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp PABPN1 est non-conjugé

Application

  • 22
  • 8
  • 6
  • 6
  • 5
  • 5
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (IHC)
  • Fonction

    PABPN1 Rabbit mAb

     Réactivité croisée

    Humain, Souris, Rat

    Attributs du produit

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogène

    A synthesized peptide derived from human PABPN1

    Isotype

    IgG
  • Indications d'application

    WB,1:500 - 1:2000, IHC,1:50 - 1:200, IF,1:50 - 1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,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

    PABPN1 (Poly A Binding Protein Nuclear 1 (PABPN1))

    Autre désignation

    PABPN1

    Sujet

    This gene encodes an abundant nuclear protein that binds with high affinity to nascent poly(A) tails. The protein is required for progressive and efficient polymerization of poly(A) tails at the 3' ends of eukaryotic transcripts and controls the size of the poly(A) tail to about 250 nt. At steady-state, this protein is localized in the nucleus whereas a different poly(A) binding protein is localized in the cytoplasm. This gene contains a GCG trinucleotide repeat at the 5' end of the coding region, and expansion of this repeat from the normal 6 copies to 8-13 copies leads to autosomal dominant oculopharyngeal muscular dystrophy (OPMD) disease. Related pseudogenes have been identified on chromosomes 19 and X. Read-through transcription also exists between this gene and the neighboring upstream BCL2-like 2 (BCL2L2) gene. [provided by RefSeq, Dec 2010],OPMD, PAB2, PABII, PABP-2, PABP2,Epigenetics & Nuclear Signaling,RNA Binding,PABPN1

    Poids moléculaire

    49kDa

    ID gène

    8106

    UniProt

    Q86U42
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