• Product nameAnti-FGF10 antibody
    See all FGF10 primary antibodies
  • Description
    Rabbit polyclonal to FGF10
  • Tested applicationsSuitable for: WB, Sandwich ELISAmore details
  • Species reactivity
    Reacts with: Human
    Predicted to work with: Mouse, Rat, Sheep, Cow, Non Human Primates
  • Immunogen

    Synthetic peptide conjugated to KLH derived from within residues 50 - 150 of Human FGF10.

    (Peptide available as ab90831.)

  • Positive control
    • This antibody gave a positive signal in the following lysates: Human Lung Tissue; A549 Whole Cell


Associated products


Our Abpromise guarantee covers the use of ab71794 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Application Abreviews Notes
WB Use a concentration of 1 µg/ml. Detects a band of approximately 37 kDa (predicted molecular weight: 23 kDa).
Sandwich ELISA Use a concentration of 0.5 µg/ml. Can be paired for Sandwich ELISA with Goat polyclonal to FGF10 (ab90207). For sandwich ELISA, use this antibody as Detection at 0.5µg/ml with Ab90207 as Capture.


  • FunctionCould be a growth factor active in the process of wound healing. Acts as a mitogen in the lung. May act in a manner similar to FGF-7.
  • Involvement in diseaseDefects in FGF10 are the cause of autosomal dominant aplasia of lacrimal and salivary glands (ALSG) [MIM:180920]. 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.
    Defects in FGF10 are a cause of lacrimo-auriculo-dento-digital syndrome (LADDS) [MIM:149730]; also known as Levy-Hollister syndrome. LADDS is a form of ectodermal dysplasia, a heterogeneous group of disorders due to abnormal development of two or more ectodermal structures. LADDS is an autosomal dominant syndrome characterized by aplastic/hypoplastic lacrimal and salivary glands and ducts, cup-shaped ears, hearing loss, hypodontia and enamel hypoplasia, and distal limb segments anomalies. In addition to these cardinal features, facial dysmorphism, malformations of the kidney and respiratory system and abnormal genitalia have been reported. Craniosynostosis and severe syndactyly are not observed.
  • Sequence similaritiesBelongs to the heparin-binding growth factors family.
  • Cellular localizationSecreted.
  • Information by UniProt
  • Database links
  • Alternative names
    • BB213776 antibody
    • fd11d03 antibody
    • FGF 10 antibody
    • FGF-10 antibody
    • FGF10 antibody
    • FGF10_HUMAN antibody
    • Fibroblast growth factor 10 antibody
    • Keratinocyte growth factor 2 antibody
    • KGF 2 antibody
    • Produced by fibroblasts of urinary bladder lamina propria antibody
    • wu:fd11d03 antibody
    • zgc:109774 antibody
    see all

Anti-FGF10 antibody images

  • Standard Curve for FGF10 (Analyte: ab73195) dilution range 1pg/ml to 1ug/ml using Capture Antibody Goat polyclonal to FGF10 (ab90207) at 5ug/ml and Detector Antibody Rabbit polyclonal to FGF10 (ab71794) at 0.5ug/ml
  • All lanes : Anti-FGF10 antibody (ab71794) at 1 µg/ml

    Lane 1 : Lung (Human) Tissue Lysate
    Lane 2 : A549 (Human lung adenocarcinoma epithelial cell line) Whole Cell Lysate

    Lysates/proteins at 10 µg per lane.

    Goat polyclonal to Rabbit IgG - H&L - Pre-Adsorbed (HRP) at 1/3000 dilution
    developed using the ECL technique

    Performed under reducing conditions.

    Predicted band size : 23 kDa
    Observed band size : 37 kDa (why is the actual band size different from the predicted?)
    Additional bands at : 170 kDa. We are unsure as to the identity of these extra bands.

    Exposure time : 1 minute

References for Anti-FGF10 antibody (ab71794)

ab71794 has not yet been referenced specifically in any publications.

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