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FOXC1 antibody (AA 404-553)

FOXC1 Reactivity: Human WB, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN1679876
  • Target See all FOXC1 Antibodies
    FOXC1 (Forkhead Box C1 (FOXC1))
    Binding Specificity
    • 8
    • 6
    • 5
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 404-553
    Reactivity
    • 48
    • 32
    • 19
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 49
    • 2
    • 1
    Rabbit
    Clonality
    • 51
    • 1
    Polyclonal
    Conjugate
    • 27
    • 6
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    This FOXC1 antibody is un-conjugated
    Application
    • 33
    • 20
    • 8
    • 8
    • 4
    • 4
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC)
    Sequence
    AAGERGGHLQ GAPGGAGGSA VDDPLPDYSL PPVTSSSSSS LSHGGGGGGG GGGQEAGHHP AAHQGRLTSW YLNQAGGDLG HLASAAAAAA AAGYPGQQQN FHSVREMFES QRIGLNNSPV NGNSSCQMAF PSSQSLYRTS GAFVYDCSKF
    Cross-Reactivity
    Human, Mouse, Rat
    Characteristics
    Polyclonal Antibodies
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein containing a sequence corresponding to amino acids 404-553 of human FOXC1 (NP_001444.2).
    Isotype
    IgG
    Top Product
    Discover our top product FOXC1 Primary Antibody
  • Application Notes
    WB,1:100 - 1:1000,IHC,1:50 - 1:100
    Restrictions
    For Research Use only
  • Buffer
    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    FOXC1 (Forkhead Box C1 (FOXC1))
    Alternative Name
    FOXC1 (FOXC1 Products)
    Background
    This gene belongs to the forkhead family of transcription factors which is characterized by a distinct DNA-binding forkhead domain. The specific function of this gene has not yet been determined, however, it has been shown to play a role in the regulation of embryonic and ocular development. Mutations in this gene cause various glaucoma phenotypes including primary congenital glaucoma, autosomal dominant iridogoniodysgenesis anomaly, and Axenfeld-Rieger anomaly.,FOXC1,ARA,ASGD3,FKHL7,FREAC-3,FREAC3,IGDA,IHG1,IRID1,RIEG3,Epigenetics & Nuclear Signaling,Transcription Factors,Cell Biology & Developmental Biology,FOXC1
    Molecular Weight
    56 kDa
    Gene ID
    2296
    UniProt
    Q12948
    Pathways
    Chromatin Binding, Glycosaminoglycan Metabolic Process
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