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FOXP2 Antikörper (AA 657-684)

FOXP2 Reaktivität: Human, Maus WB, IF Wirt: Kaninchen Polyclonal RB21207 unconjugated
Produktnummer ABIN651939
  • Target Alle FOXP2 Antikörper anzeigen
    FOXP2 (Forkhead Box P2 (FOXP2))
    Bindungsspezifität
    • 10
    • 10
    • 6
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 657-684
    Reaktivität
    • 46
    • 23
    • 15
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Maus
    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
    • 14
    • 7
    • 6
    • 5
    • 3
    • 3
    Western Blotting (WB), Immunofluorescence (IF)
    Homologie
    Rat
    Aufreinigung
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    Immunogen
    This FOXP2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 657-684 amino acids of human FOXP2.
    Klon
    RB21207
    Isotyp
    IgG
    Top Product
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  • Applikationshinweise
    IF: 1:10~50. WB: 1:1000
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Buffer
    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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
    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.
    Haltbarkeit
    6 months
  • Vibulyaseck, Fujita, Luo, Tran, Oh-Nishi, Ono, Hirano, Sugihara: "Spatial rearrangement of Purkinje cell subsets forms the transverse and longitudinal compartmentalization in the mouse embryonic cerebellum." in: The Journal of comparative neurology, Vol. 525, Issue 14, pp. 2971-2990, (2018) (PubMed).

    Fujita, Morita, Furuichi, Sugihara: "Clustered fine compartmentalization of the mouse embryonic cerebellar cortex and its rearrangement into the postnatal striped configuration." in: The Journal of neuroscience : the official journal of the Society for Neuroscience, Vol. 32, Issue 45, pp. 15688-703, (2012) (PubMed).

  • 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
    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.
    Molekulargewicht
    79919
    Gen-ID
    93986
    NCBI Accession
    NP_001166237, NP_001166238, NP_055306, NP_683696, NP_683697, NP_683698
    UniProt
    O15409
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