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FOXC1 Antikörper (AA 101-200)

FOXC1 Reaktivität: Human, Maus, Ratte, Ziege WB, ELISA, IHC (p), FACS, IF (cc), IF (p), IHC (fro) Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN719291
  • Target Alle FOXC1 Antikörper anzeigen
    FOXC1 (Forkhead Box C1 (FOXC1))
    Bindungsspezifität
    • 11
    • 8
    • 5
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 101-200
    Reaktivität
    • 53
    • 32
    • 18
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human, Maus, Ratte, Ziege
    Wirt
    • 54
    • 2
    • 1
    Kaninchen
    Klonalität
    • 56
    • 1
    Polyklonal
    Konjugat
    • 27
    • 7
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    Dieser FOXC1 Antikörper ist unkonjugiert
    Applikation
    • 38
    • 25
    • 8
    • 7
    • 3
    • 3
    • 3
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
    Kreuzreaktivität
    Ziege, Human, Maus, Ratte
    Homologie
    Dog,Cow,Horse,Chicken
    Aufreinigung
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human FOXC1/FREAC3
    Isotyp
    IgG
    Top Product
    Discover our top product FOXC1 Primärantikörper
  • Applikationshinweise
    WB 1:300-5000
    ELISA 1:500-1000
    FCM 1:20-100
    IHC-P 1:200-400
    IHC-F 1:100-500
    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 μg/μL
    Buffer
    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
    Konservierungsmittel
    ProClin
    Vorsichtsmaßnahmen
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Lagerung
    4 °C,-20 °C
    Informationen zur Lagerung
    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
    Haltbarkeit
    12 months
  • Target
    FOXC1 (Forkhead Box C1 (FOXC1))
    Andere Bezeichnung
    FREAC3 (FOXC1 Produkte)
    Synonyme
    ARA antikoerper, FKHL7 antikoerper, FREAC-3 antikoerper, FREAC3 antikoerper, IGDA antikoerper, IHG1 antikoerper, IRID1 antikoerper, RIEG3 antikoerper, FoxC1 antikoerper, fkhl7 antikoerper, freac-3 antikoerper, freac3 antikoerper, igda antikoerper, ihg1 antikoerper, irid1 antikoerper, rieg3 antikoerper, xfd-11 antikoerper, ara antikoerper, FOXC1 antikoerper, foxc1 antikoerper, Fkh1 antikoerper, Mf1 antikoerper, Mf4 antikoerper, ch antikoerper, fkh-1 antikoerper, frkhda antikoerper, CFKH-1 antikoerper, XFD-11 antikoerper, foxc1.2 antikoerper, id:ibd5079 antikoerper, forkhead box C1 antikoerper, forkhead box C1 S homeolog antikoerper, forkhead box C1 L homeolog antikoerper, Forkhead box protein C1 antikoerper, winged helix transcription factor XFD-11 antikoerper, forkhead box C1b antikoerper, FOXC1 antikoerper, Foxc1 antikoerper, foxc1.S antikoerper, foxc1 antikoerper, foxc1.L antikoerper, foxc1-A antikoerper, foxc1b antikoerper
    Hintergrund

    Synonyms: ARA, FKH L7, FKHL 7, FKHL7, Forkhead Drosophila like 7, Forkhead, forkhead box C1, Forkhead box protein C1,Forkhead drosophila homolog like 7, Forkhead like 7, Forkhead related activator 3, Forkhead related protein FKHL7, Forkhead related transcription factor 3, Forkhead-related protein FKHL7, Forkhead-related transcription factor 3, FOX C1, FOXC 1, FOXC1, FOXC1_HUMAN, FREAC 3,FREAC-3, FREAC3, homolog-like 7, IGDA, IHG 1, IHG1, IRID 1, IRID1, Iridogoniodysgenesis type 1, Myeloid factor delta.

    Background: Binding of FREAC-3 and FREAC-4 to their cognate sites results in bending of the DNA at an angle of 80-90 degrees.Involvement in disease, Defects in FOXC1 are the cause of Axenfeld-Rieger syndrome type 3 (RIEG3), also known as Axenfeld-Rieger syndrome (ARS) or Axenfeld syndrome or Axenfeld anomaly. It is characterized by posterior corneal embryotoxon, prominent Schwalbe line and iris adhesion to the Schwalbe line. Other features may be hypertelorism (wide spacing of the eyes), hypoplasia of the malar bones, congenital absence of some teeth and mental retardation. When associated with tooth anomalies, the disorder is known as Rieger syndrome. Glaucoma is a progressive blinding condition that occurs in approximately half of patients with Axenfeld-Rieger malformations.

    Gen-ID
    2296
    Pathways
    Chromatin Binding, Glycosaminoglycan Metabolic Process
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