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FOXP2 Antikörper (C-Term)

Dieses Anti-FOXP2-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von FOXP2 in . Geeignet für Human und Maus.
Produktnummer ABIN6295056

Kurzübersicht für FOXP2 Antikörper (C-Term) (ABIN6295056)

Target

Alle FOXP2 Antikörper anzeigen
FOXP2 (Forkhead Box P2 (FOXP2))

Reaktivität

  • 45
  • 23
  • 14
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Maus

Wirt

  • 33
  • 7
  • 3
  • 2
  • 1
Kaninchen

Klonalität

  • 35
  • 10
  • 1
Polyklonal

Konjugat

  • 32
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser FOXP2 Antikörper ist unkonjugiert

Applikation

Bitte anfragen
  • Bindungsspezifität

    • 10
    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 657-684, C-Term

    Verwendungszweck

    Rabbit Anti-FOXP2 (C-term) Antibody

    Immunogen

    This FOXP2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 657-684 amino acids from the C-terminal region of human FOXP2.
  • Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    2-8°C (short-term), -20°C (long-term)
  • Target

    FOXP2 (Forkhead Box P2 (FOXP2))

    Andere Bezeichnung

    FOXP2

    Hintergrund

    Target Description: FOXP2 is 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. Multiple alternative transcripts encoding different isoforms have been identified in this gene.

    Gene Symbol: FOXP2

    Gen-ID

    93986

    UniProt

    O15409
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