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FOXP2 Antikörper (AA 637-715)

FOXP2 Reaktivität: Human, Maus, Ratte WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN5518915
  • Target Alle FOXP2 Antikörper anzeigen
    FOXP2 (Forkhead Box P2 (FOXP2))
    Bindungsspezifität
    • 11
    • 10
    • 6
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 637-715
    Reaktivität
    • 46
    • 23
    • 14
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Maus, Ratte
    Wirt
    • 35
    • 7
    • 3
    • 1
    • 1
    Kaninchen
    Klonalität
    • 38
    • 8
    • 1
    Polyklonal
    Konjugat
    • 29
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser FOXP2 Antikörper ist unkonjugiert
    Applikation
    • 35
    • 29
    • 15
    • 7
    • 6
    • 5
    • 3
    • 3
    Western Blotting (WB)
    Verwendungszweck
    Rabbit IgG polyclonal antibody for Forkhead box protein P2(FOXP2) detection. Tested with WB in Human,Mouse,Rat.
    Kreuzreaktivität (Details)
    No cross reactivity with other proteins.
    Produktmerkmale
    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
    Aufreinigung
    Immunogen affinity purified.
    Immunogen
    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.
    Isotyp
    IgG
    Top Product
    Discover our top product FOXP2 Primärantikörper
  • Applikationshinweise
    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.
    Kommentare

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

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Rekonstitution
    Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.
    Konzentration
    500 μg/mL
    Buffer
    Each vial contains 5 mg BSA, 0.9 mg NaCl, 0.2 mg Na2HPO4, 0.05 mg Sodium azide.
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    4 °C,-20 °C
    Informationen zur Lagerung
    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.
  • Target
    FOXP2 (Forkhead Box P2 (FOXP2))
    Andere Bezeichnung
    FOXP2 (FOXP2 Produkte)
    Synonyme
    CAGH44 antikoerper, SPCH1 antikoerper, TNRC10 antikoerper, 2810043D05Rik antikoerper, AI449000 antikoerper, CAG-16 antikoerper, D0Kist7 antikoerper, RGD1559697 antikoerper, FOXP2 antikoerper, spch1 antikoerper, cagh44 antikoerper, tnrc10 antikoerper, xlFoxP2 antikoerper, foxP2 antikoerper, foxP antikoerper, Foxp2 antikoerper, foxP2b antikoerper, foxp2a antikoerper, forkhead box P2 antikoerper, lmw-gs antikoerper, forkhead box transcription factor antikoerper, forkhead box P2 L homeolog antikoerper, FOXP2 antikoerper, Foxp2 antikoerper, foxp2 antikoerper, foxP2 antikoerper, foxp1c antikoerper, foxp2.L antikoerper
    Hintergrund
    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
    Gen-ID
    93986
    UniProt
    O15409
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