• merck millipore,默克密理博,ABN44,Anti-FGF10 Antibody
  • merck millipore,默克密理博,ABN44,Anti-FGF10 Antibody

    产品名称:Anti-FGF10 Antibody
    产品型号:ABN44
    Detect FGF10 using this Anti-FGF10 Antibody validated for use in WB, IH(P).

    merck millipore,默克密理博,ABN44,Anti-FGF10 Antibody

  • 产品介绍
  • merck millipore,默克密理博,ABN44,Anti-FGF10 Antibody

    重要规格表

    品种反应性 主要应用 宿主 格式 抗体类型
    Rhesus Macaque, H, M, RWBRbAffinity PurifiedPolyclonal Antibody
    描述
    产品目录编号 ABN44
    描述 Anti-FGF10 Antibody
    Alternate Names
    • Keratinocyte growth factor 2
    • Fibroblast growth factor 10
    • FGF-10
    背景信息 Fibroblast growth factor 10 (FGF10) is a member of the fibroblast growth factor family and plays an essential role in the regulation of cell differentiation, tissue repair, tumor growth, embryonic development, and cell proliferation. Mutations in FGF10 have been associated lacrimo-auriculo-dento-digital syndrome (LADDS) which is a form of ectodermal dysplasia.
    产品信息
    格式 Affinity Purified
    控制
    • A549 cell lysate
    演示 Purified Rabbit Polyclonal in buffer containing 0.1 M Tris-Glycine (pH 7.4) and 150 mM NaCl with 0.05% sodium azide.
    应用
    应用 Detect FGF10 using this Anti-FGF10 Antibody validated for use in WB, IH(P).
    主要应用
    • Western Blotting
    应用说明 Western Blot Analysis: 0.5 µg/mL from a representative lot detected FGF10 on 10 µg of mouse embryo tissue lysate.

    Immunohistochemistry Analysis: A 1:1,000 dilution from a representative lot detected FGF10 in mouse epithelial cells, mouse liver, human brain, and human cerebellum tissues.
    生物信息
    免疫原品种 KLH-conjugated linear peptide corresponding to human FGF10.
    浓缩 Please refer to the Certificate of Analysis for the lot-specific concentration.
    宿主 Rabbit
    品种反应性 Rhesus MacaqueHumanMouseRat
    Species Reactivity Note Demonstrated to react with Human, Mouse, and Rat. Predicted to react with Rhesus Macaque based on 100% sequence homology.
    抗体类型 Polyclonal Antibody
    Entrez基因编号
    • NP_004456
    Entrez基因汇总 The protein encoded by this gene 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. This protein exhibits mitogenic activity for keratinizing epidermal cells, but essentially no activity for fibroblasts, which is similar to the biological activity of FGF7. Studies of the mouse homolog of suggested that this gene is required for embryonic epidermal morphogenesis including brain development, lung morphogenesis, and initiation of lim bud formation. This gene is also implicated to be a primary factor in the process of wound healing. [provided by RefSeq, Jul 2008].
    基因符号
    • FGF10
    纯化方法 Affinity purified
    UniProt编号
    • O15520
    UniProt汇总 FUNCTION: Plays an important role in the regulation of embryonic development, cell proliferation and cell differentiation. Required for normal branching morphogenesis. May play a role in wound healing. Ref.8

    SUBUNIT STRUCTURE: Interacts with FGFR1 and FGFR2. Interacts with FGFBP1. Ref.7 Ref.8

    SUBCELLULAR LOCATION: Secreted Potential.

    INVOLVEMENT IN DISEASE: Defects 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. Ref.11

    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. Ref.12 Ref.13

    SEQUENCE SIMILARITIES: Belongs to the heparin-binding growth factors family.
    产品使用声明
    质量保证 Evaluated by Western Blot in A549 cell lysate.

    Western Blot Analysis: 0.5 µg/mL of this antibody detected FGF10 on 10 µg of A549 cell lysate.
    使用声明
    • Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
    储存和货运信息
    存储条件 Stable for 1 year at 2-8°C from date of receipt.
    包装信息
    数量 100 µg

    merck millipore,默克密理博,ABN44,Anti-FGF10 Antibody

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