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PSPC1 anticorps

L’anticorps Lapin Polyclonal anti-PSPC1 a été validé pour ELISA et IHC. Il convient pour détecter PSPC1 dans des échantillons de Humain, Souris et Rat.
N° du produit ABIN7246601

Aperçu rapide pour PSPC1 anticorps (ABIN7246601)

Antigène

Voir toutes PSPC1 Anticorps
PSPC1 (Paraspeckle Component 1 (PSPC1))

Reactivité

  • 15
  • 7
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 15
Lapin

Clonalité

  • 15
Polyclonal

Conjugué

  • 12
  • 1
  • 1
  • 1
Cet anticorp PSPC1 est non-conjugé

Application

  • 11
  • 7
  • 6
  • 4
  • 3
  • 3
  • 1
  • 1
ELISA, Immunohistochemistry (IHC)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogène

    Fusion protein of human PSPC1

    Isotype

    IgG
  • Indications d'application

    IHC 1:30-1:150, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.54 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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

    PSPC1 (Paraspeckle Component 1 (PSPC1))

    Autre désignation

    PSPC1

    Sujet

    This gene encodes a nucleolar protein that localizes to punctate subnuclear structures that occur close to splicing speckles, known as paraspeckles. These paraspeckles are composed of RNA-protein structures that include a non-coding RNA, NEAT1/Men epsilon/beta, and the Drosophila Behavior Human Splicing family of proteins, which include the product of this gene and the P54NRB/NONO and PSF/SFPQ proteins. Paraspeckles may function in the control of gene expression via an RNA nuclear retention mechanism. The protein encoded by this gene is found in paraspeckles in transcriptionally active cells, but it localizes to unique cap structures at the nucleolar periphery when RNA polymerase II transcription is inhibited, or during telophase. Alternative splicing of this gene results in multiple transcript variants. A related pseudogene, which is also located on chromosome 13, has been identified.

    UniProt

    Q8WXF1
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