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RBM17 anticorps (AA 25-75)

Cet anticorps Lapin Polyclonal détecte spécifiquement RBM17 dans WB, IP et IHC (fp). Il présente une réactivité envers Humain et Souris.
N° du produit ABIN7453552

Aperçu rapide pour RBM17 anticorps (AA 25-75) (ABIN7453552)

Antigène

Voir toutes RBM17 Anticorps
RBM17 (RNA Binding Motif Protein 17 (RBM17))

Reactivité

  • 19
  • 6
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Humain, Souris

Hôte

  • 18
  • 3
Lapin

Clonalité

  • 19
  • 2
Polyclonal

Conjugué

  • 14
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp RBM17 est non-conjugé

Application

  • 10
  • 8
  • 6
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunoprecipitation (IP), Immunohistochemistry (Formalin-fixed Paraffin-embedded Sections) (IHC (fp))
  • Épitope

    • 2
    • 2
    • 2
    • 2
    AA 25-75

    Fonction

    Rabbit anti-SPF45 Antibody, Affinity Purified

    Purification

    Affinity Purified

    Immunogène

    between AA 25 and 75

    Isotype

    IgG
  • Indications d'application

    IHC: 1:1,000 - 1:5,000. Epitope retrieval with citrate buffer pH 6.0 is recommended for FFPE tissue sections.

    IP: 2 - 10 μg/mg lysate

    WB: Not recommended. Use rabbit anti-SPF45 antibody ABIN7453790.

    Restrictions

    For Research Use only
  • Concentration

    1000 μg/mL

    Buffer

    Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % Sodium Azide

    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

    4 °C

    Date de péremption

    12 months
  • Antigène

    RBM17 (RNA Binding Motif Protein 17 (RBM17))

    Autre désignation

    SPF45

    Sujet

    Background: Splicing factor 45 (SPF45) is an RNA splicing factor that binds to the single stranded 3'AG at the exon/intron border and promotes its utilization in the second catalytic step. SPF45 is involved in the regulation of alternative splicing and the utilization of cryptic splice sites. It has been shown to promote the utilization of a cryptic splice site created by the beta-110 mutation in the human beta-thalassemia gene. The resulting frameshift leads to sickle cell anemia [taken from the Universal Protein Resource (UniProt) Q96125].

    ID gène

    84991

    NCBI Accession

    NP_116294

    UniProt

    Q96I25
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