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FOXP2 anticorps (AA 637-715)

FOXP2 Reactivité: Humain, Souris, Rat WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN5518915
  • Antigène Voir toutes FOXP2 Anticorps
    FOXP2 (Forkhead Box P2 (FOXP2))
    Épitope
    • 11
    • 10
    • 6
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 637-715
    Reactivité
    • 46
    • 23
    • 14
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain, Souris, Rat
    Hôte
    • 35
    • 7
    • 3
    • 1
    • 1
    Lapin
    Clonalité
    • 38
    • 8
    • 1
    Polyclonal
    Conjugué
    • 29
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp FOXP2 est non-conjugé
    Application
    • 35
    • 29
    • 15
    • 7
    • 6
    • 5
    • 3
    • 3
    Western Blotting (WB)
    Fonction
    Rabbit IgG polyclonal antibody for Forkhead box protein P2(FOXP2) detection. Tested with WB in Human,Mouse,Rat.
    Réactivité croisée (Details)
    No cross reactivity with other proteins.
    Attributs du produit
    Rabbit IgG polyclonal antibody for Forkhead box protein P2(FOXP2) detection. Tested with WB in Human,Mouse,Rat.
    Gene Name: forkhead box P2
    Protein Name: Forkhead box protein P2
    Purification
    Immunogen affinity purified.
    Immunogène
    E. coli-derived human FOXP2 recombinant protein (Position: L637-E715). Human FOXP2 shares 100% amino acid (aa) sequence identity with both mouse and rat FOXP2.
    Isotype
    IgG
    Top Product
    Discover our top product FOXP2 Anticorps primaire
  • Indications d'application
    WB: Concentration: 0.1-0.5 μg/mL, Tested Species: Human, Mouse, Rat
    Notes: Tested Species: Species with positive results.
    Other applications have not been tested. Optimal dilutions should be determined by end users.
    Commentaires

    Boster recommends Enhanced Chemiluminescent Kit with anti-Rabbit IgG (ABIN921124) for Western blot.

    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.
    Concentration
    500 μg/mL
    Buffer
    Each vial contains 5 mg BSA, 0.9 mg NaCl, 0.2 mg Na2HPO4, 0.05 mg 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,-20 °C
    Stockage commentaire
    At -20°C for one year. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20 °C for a longer time. Avoid repeated freezing and thawing.
  • Antigène
    FOXP2 (Forkhead Box P2 (FOXP2))
    Autre désignation
    FOXP2 (FOXP2 Produits)
    Synonymes
    anticorps CAGH44, anticorps SPCH1, anticorps TNRC10, anticorps 2810043D05Rik, anticorps AI449000, anticorps CAG-16, anticorps D0Kist7, anticorps RGD1559697, anticorps FOXP2, anticorps spch1, anticorps cagh44, anticorps tnrc10, anticorps xlFoxP2, anticorps foxP2, anticorps foxP, anticorps Foxp2, anticorps foxP2b, anticorps foxp2a, anticorps forkhead box P2, anticorps lmw-gs, anticorps forkhead box transcription factor, anticorps forkhead box P2 L homeolog, anticorps FOXP2, anticorps Foxp2, anticorps foxp2, anticorps foxP2, anticorps foxp1c, anticorps foxp2.L
    Sujet
    Forkhead box protein P2 (FOXP2) is a protein that, in humans, is encoded by the FOXP2 gene. This gene encodes a member of the forkhead/winged-helix (FOX) family of transcription factors. It is expressed in fetal and adult brain as well as in several other organs such as the lung and gut. The protein product contains a FOX DNA-binding domain and a large polyglutamine tract and is an evolutionarily conserved transcription factor, which may bind directly to approximately 300 to 400 gene promoters in the human genome to regulate the expression of a variety of genes. This gene is required for proper development of speech and language regions of the brain during embryogenesis, and may be involved in a variety of biological pathways and cascades that may ultimately influence language development. Mutations in this gene cause speech-language disorder 1 (SPCH1), also known as autosomal dominant speech and language disorder with orofacial dyspraxia.

    Synonyms: Forkhead box protein P2, CAG repeat protein 44, Trinucleotide repeat-containing gene 10 protein, FOXP2, CAGH44, TNRC10
    ID gène
    93986
    UniProt
    O15409
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