Anti-FGF10 / KGF2 antibody

Cat.#: 106126

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Product Information

  • Product Name
    Anti-FGF10 / KGF2 antibody
  • Documents
  • Description
    Rabbit polyclonal to FGF10 / KGF2
  • Tested applications
    WB
  • Species reactivity
    Human FGF10 / KGF2
  • Alternative names
    AEY17 antibody; Fgf-10 antibody; BB213776 antibody; Gsfaey17 antibody; BB213776 antibody; Fgf10 antibody; FGF10 antibody; Fgf-10 antibody; keratinocyte growth factor 2 antibody; produced by fibroblasts of urinary bladder lamina propria antibody
  • Immunogen
  • Isotype
    Rabbit IgG
  • Preparation
    Produced in rabbits immunized with purified, recombinant Human FGF10 / KGF2 (rh FGF10 / KGF2; NP_004456.1; Gln38-Ser208). FGF10 / KGF2 specific IgG was purified by Human FGF10 / KGF2 affinity chromatography.
  • Clonality
    Polyclonal
  • Formulation
    0.2 μm filtered solution in PBS
  • Storage instructions
    This antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -80℃. Preservative-Free.
    Sodium azide is recommended to avoid contamination (final concentration 0.05%-0.1%). It is toxic to cells and should be disposed of properly. Avoid repeated freeze-thaw cycles.
  • Applications

    WB: 5-10 μg/ml

  • Validations

    FGF10 Antibody, Rabbit PAb, Antigen Affinity Purified, Western blot

    FGF10 Antibody, Rabbit PAb, Antigen Affinity Purified, Western blot

  • Background
    Fibroblast growth factor 10 (FGF10) is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. FGF10 exhibits mitogenic activity for keratinizing epidermal cells, but essentially no activity for fibroblasts, which is similar to the biological activity of FGF7. FGF10 plays an important role in the regulation of embryonic development, cell proliferation and cell differentiation. FGF10 is required for normal branching morphogenesis. It may play a role in wound healing. Defects in FGF10 are the cause of autosomal dominant aplasia of lacrimal and salivary glands (ALSG). ALSG has variable expressivity, and affected individuals may have aplasia or hypoplasia of the lacrimal, parotid, submandibular and sublingual glands and absence of the lacrimal puncta. The disorder is characterized by irritable eyes, recurrent eye infections, epiphora (constant tearing) and xerostomia (dryness of the mouth), which increases the risk of dental erosion, dental caries, periodontal disease and oral infections.
  • References
    • Sekine K, et al. (1999) Fgf10 is essential for limb and lung formation. Nat Genet. 21(1): 138-41.
    • Ohuchi H, et al. (2000) FGF10 acts as a major ligand for FGF receptor 2 IIIb in mouse multi-organ development. Biochem Biophys Res Commun. 277(3): 643-9.
    • Bellusci S, et al. (1997) Fibroblast growth factor 10 (FGF10) and branching morphogenesis in the embryonic mouse lung. Development. 124(23): 4867-78.

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"