FOXC1 Antibody

Forkhead box C1 (FOXC1) belongs to the forkhead family of transcription factors which is characterized by a distinct DNA-binding forkhead domain. The specific function of FOXC1 has not yet been determined; however, the gene has been shown to play a role in the regulation of embryonic and ocular development. Mutations in the FOXC1 gene cause various glaucoma phenotypes including primary congenital glaucoma, autosomal dominant iridogoniodysgenesis anomaly, and Axenfeld-Rieger anomaly.[taken from NCBI Entrez Gene (Gene ID: 2296)].
    Product Specifications
    Catalog # Size Price
    FOXC1 AntibodyReactivity: Human
    Applications: IP, IHC-P, IF
    Immunogen: Between 275 and 325
    A303-519A100 µl (1 mg/ml) $339Add to Cart
    A303-519A-T10 µl (1 mg/ml) $50Add to Cart
    FOXC1 AntibodyReactivity: Human
    Applications: WB, IP, IHC-P, IF
    Immunogen: Between 375 and 425
    A303-520A100 µl (0.2 mg/ml) $339Add to Cart
    A303-520A-M100 µl (10 blots) $229Add to Cart
    A303-520A-T20 µl (2 blots) $50Add to Cart

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