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RBM28 anticorps (AA 18-584)

L’anticorps anti-RBM28 Polyclonal Lapin est utilisé pour la détection de RBM28 dans des échantillons de Humain. Il a été validé pour WB, ELISA et FACS.
N° du produit ABIN7871430
644,88 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour RBM28 anticorps (AA 18-584) (ABIN7871430)

Antigène

Voir toutes RBM28 Anticorps
RBM28 (RNA Binding Motif Protein 28 (RBM28))

Reactivité

  • 24
  • 5
  • 5
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
Humain

Hôte

  • 24
Lapin

Clonalité

  • 24
Polyclonal

Conjugué

  • 19
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp RBM28 est non-conjugé

Application

  • 24
  • 11
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • Épitope

    • 8
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 18-584

    Fonction

    RBM28 Antibody / RNA-binding protein 28

    Purification

    Antigen affinity purified

    Immunogène

    Recombinant human protein (amino acids E18-K584) was used as the immunogen for the RBM28 antibody.

    Isotype

    IgG
  • Indications d'application

    Optimal dilution of the RBM28 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Stock

    4 °C,-20 °C

    Stockage commentaire

    After reconstitution, the RBM28 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Antigène

    RBM28 (RNA Binding Motif Protein 28 (RBM28))

    Autre désignation

    RBM28

    Sujet

    RNA-binding protein 28 is a protein that in humans is encoded by the RBM28 gene. The protein encoded by this gene is a specific nucleolar component of the spliceosomal small nuclear ribonucleoprotein (snRNP)complexes . It specifically associates with U1, U2, U4, U5, and U6 small nuclear RNAs (snRNAs), possibly coordinating their transition through the nucleolus. Mutation in this gene causes alopecia, progressive neurological defects, and endocrinopathy (ANE syndrome), a pleiotropic and clinically heterogeneous disorder. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

    UniProt

    Q9NW13

    Pathways

    SARS-CoV-2 Protein Interactome
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