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ACTL10 anticorps (AA 21-100) (HRP)

Cet anticorps Lapin Polyclonal détecte spécifiquement ACTL10 dans ELISA, IHC (fro) et IHC (p). Il présente une réactivité envers Rat.
N° du produit ABIN1711234

Aperçu rapide pour ACTL10 anticorps (AA 21-100) (HRP) (ABIN1711234)

Antigène

ACTL10 (Actin-Like 10 (ACTL10))

Reactivité

Rat

Hôte

  • 14
Lapin

Clonalité

  • 14
Polyclonal

Conjugué

  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp ACTL10 est conjugé à/à la HRP

Application

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

    AA 21-100

     Réactivité croisée

    Rat

    Homologie

    Human,Mouse

    Purification

    Purified by Protein A.

    Immunogène

    KLH conjugated synthetic peptide derived from human C20orf134

    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

    ACTL10 (Actin-Like 10 (ACTL10))

    Autre désignation

    C20orf134

    Sujet

    Synonyms: C20orf134, CT134_HUMAN, Putative uncharacterized actin family protein C20orf134.

    Background: C20orf134 is a 245 amino acid secreted protein that belongs to the Actin family and is encoded by a gene which maps to human chromosome 20. Comprising approximately 2 % of the human genome, chromosome 20 contains nearly 63 million bases that encode over 600 genes, some of which are associated with Creutzfeldt-Jakob disease, amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome. Additionally, chromosome 20 contains a region with numerous genes which are thought important for seminal production and may be potential targets for male contraception.

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