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FRAS1 anticorps (AA 1101-1200) (HRP)

Cet anticorps anti-FRAS1 est un anticorps Lapin Polyclonal détectant FRAS1 dans ELISA, IHC (fro) et IHC (p). Adapté pour Humain.
N° du produit ABIN1711305

Aperçu rapide pour FRAS1 anticorps (AA 1101-1200) (HRP) (ABIN1711305)

Antigène

Voir toutes FRAS1 Anticorps
FRAS1 (Fraser Syndrome 1 (FRAS1))

Reactivité

  • 16
  • 1
  • 1
Humain

Hôte

  • 16
Lapin

Clonalité

  • 16
Polyclonal

Conjugué

  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp FRAS1 est conjugé à/à la HRP

Application

  • 13
  • 13
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Épitope

    • 14
    • 1
    AA 1101-1200

    Homologie

    Human,Mouse,Rat

    Purification

    Purified by Protein A.

    Immunogène

    KLH conjugated synthetic peptide derived from human FRAS1

    Isotype

    IgG
  • Indications d'application

    IHC-P 1:200-400
    IHC-F 1:100-500

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    Agent conservateur

    ProClin

    Précaution d'utilisation

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

    Conseil sur la manipulation

    Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.

    Stock

    -20 °C

    Stockage commentaire

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    Date de péremption

    12 months
  • Antigène

    FRAS1 (Fraser Syndrome 1 (FRAS1))

    Autre désignation

    FRAS1

    Sujet

    Synonyms: Extracellular matrix protein FRAS1, Fras 1, Fras1, FRAS1_HUMAN, Fraser syndrome 1.

    Background: This gene encodes an extracellular matrix protein that appears to function in the regulation of epidermal-basement membrane adhesion and organogenesis during development. Mutations in this gene cause Fraser syndrome, a multisystem malformation that can include craniofacial, urogenital and respiratory system abnormalities. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009].

    ID gène

    80144

    UniProt

    Q86XX4
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