Recombinant人FGF8 protein (ab50128)

概述

描述

  • 性质Recombinant
  • 来源Escherichia coli
  • 氨基酸序列
    • 种属Human
    • 序列MQVTVQSSPN FTQHVREQSL VTDQLSRRLI RTYQLYSRTS GKHVQVLANK RINAMAEDGD PFAKLIVETD TFGSRVRVRG AETGLYICMN KKGKLIAKSN GKGKDCVFTE IVLENNYTAL QNAKYEGWYM AFTRKGRPRK GSKTRQHQRE VHFMKRLPRG HHTTEQSLRF EFLNYPPFTR SLRGSQRTWA PEPR

技术指标

Our Abpromise guarantee covers the use of ab50128 in the following tested applications.

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

  • 应用

    SDS-PAGE

    Functional Studies

  • 内毒素水平< 0.100 Eu/µg
  • 纯度> 95 % SDS-PAGE.
    Greater than 95% by SDS-PAGE.
  • 形式Lyophilised
  • Concentration information loading...

制备和贮存

  • 稳定性和存储

    Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.

    pH: 8.00
    Constituents: 0.164% Sodium phosphate, 0.44% Sodium chloride

  • 复溶Centrifuge the vial prior to opening. Reconstitute in 10 mM Tris pH 8.0 to a concentration of 0.1-1.0 mg/ml. This solution can then be diluted into other aqueous buffers and stored at 4oC for 1 week or -20oC for future use. Repeated freeze thaw cycles will result in some loss of activity.

常规信息

  • 别名
    • AIGF
    • Androgen induced growth factor
    • Androgen-induced growth factor
    • FGF 8
    • FGF-8
    • FGF8
    • FGF8_HUMAN
    • Fibroblast growth factor 8
    • Fibroblast growth factor 8 (androgen induced)
    • Fibroblast growth factor 8 precursor
    • HBGF 8
    • HBGF-8
    • HBGF8
    • Heparin-binding growth factor 8
    • HH6
    • KAL6
    see all
  • 功能Stimulates growth of the cells in an autocrine manner. Mediates hormonal action on the growth of cancer cells.
  • 疾病相关Defects in FGF8 are the cause of Kallmann syndrome type 6 (KAL6) [MIM:612702]. Kallmann syndrome is a disorder that associates hypogonadotropic hypogonadism and anosmia. Anosmia or hyposmia is related to the absence or hypoplasia of the olfactory bulbs and tracts. Hypogonadism is due to deficiency in gonadotropin-releasing hormone and probably results from a failure of embryonic migration of gonadotropin-releasing hormone-synthesizing neurons. In some patients other developmental anomalies can be present, which include renal agenesis, cleft lip and/or palate, selective tooth agenesis, and bimanual synkinesis. In some cases anosmia may be absent or inconspicuous.
    Defects in FGF8 are a cause of idiopathic hypogonadotropic hypogonadism (IHH) [MIM:146110]. IHH is defined as a deficiency of the pituitary secretion of follicle-stimulating hormone and luteinizing hormone, which results in the impairment of pubertal maturation and of reproductive function.
  • 序列相似性Belongs to the heparin-binding growth factors family.
  • 发展阶段In adults expression is restricted to the gonads.
  • 细胞定位Secreted.
  • Information by UniProt

Recombinant Human FGF8 protein (ab50128)参考文献

ab50128 has not yet been referenced specifically in any publications.

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