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FOXC1 anticorps (AA 101-200)

FOXC1 Reactivité: Humain, Souris, Rat, Chévre WB, ELISA, FACS, IHC (p), IF (cc), IF (p), IHC (fro) Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN719291
  • Antigène Voir toutes FOXC1 Anticorps
    FOXC1 (Forkhead Box C1 (FOXC1))
    Épitope
    • 11
    • 8
    • 5
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 101-200
    Reactivité
    • 53
    • 31
    • 18
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Humain, Souris, Rat, Chévre
    Hôte
    • 54
    • 2
    • 1
    Lapin
    Clonalité
    • 56
    • 1
    Polyclonal
    Conjugué
    • 27
    • 7
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    Cet anticorp FOXC1 est non-conjugé
    Application
    • 38
    • 24
    • 9
    • 8
    • 4
    • 3
    • 3
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB), ELISA, Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
     Réactivité croisée
    Chévre, Humain, Souris, Rat
    Homologie
    Dog,Cow,Horse,Chicken
    Purification
    Purified by Protein A.
    Immunogène
    KLH conjugated synthetic peptide derived from human FOXC1/FREAC3
    Isotype
    IgG
    Top Product
    Discover our top product FOXC1 Anticorps primaire
  • Indications d'application
    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
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 μg/μL
    Buffer
    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
    Agent conservateur
    ProClin
    Précaution d'utilisation
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Stock
    4 °C,-20 °C
    Stockage commentaire
    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
    Date de péremption
    12 months
  • Antigène
    FOXC1 (Forkhead Box C1 (FOXC1))
    Autre désignation
    FREAC3 (FOXC1 Produits)
    Synonymes
    anticorps ARA, anticorps FKHL7, anticorps FREAC-3, anticorps FREAC3, anticorps IGDA, anticorps IHG1, anticorps IRID1, anticorps RIEG3, anticorps FoxC1, anticorps fkhl7, anticorps freac-3, anticorps freac3, anticorps igda, anticorps ihg1, anticorps irid1, anticorps rieg3, anticorps xfd-11, anticorps ara, anticorps FOXC1, anticorps foxc1, anticorps Fkh1, anticorps Mf1, anticorps Mf4, anticorps ch, anticorps fkh-1, anticorps frkhda, anticorps CFKH-1, anticorps XFD-11, anticorps foxc1.2, anticorps id:ibd5079, anticorps forkhead box C1, anticorps forkhead box C1 S homeolog, anticorps forkhead box C1 L homeolog, anticorps Forkhead box protein C1, anticorps winged helix transcription factor XFD-11, anticorps forkhead box C1b, anticorps FOXC1, anticorps Foxc1, anticorps foxc1.S, anticorps foxc1, anticorps foxc1.L, anticorps foxc1-A, anticorps foxc1b
    Sujet

    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.

    ID gène
    2296
    Pathways
    Chromatin Binding, Glycosaminoglycan Metabolic Process
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