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Fibroblast Growth Factor 13 (FGF13) (Middle Region) Peptide

FGF13 适用: 人 宿主: 合成 BP, WB
产品编号 ABIN976828
发货至: 中国
  • 抗原 See all FGF13 products
    FGF13 (Fibroblast Growth Factor 13 (FGF13))
    蛋白结构域
    Middle Region
    宿主
    资源
    • 9
    合成
    应用范围
    Blocking Peptide (BP), Western Blotting (WB)
    产品特性
    This is a synthetic peptide designed for use in combination with anti-FGF13 antibody (Catalog #: ARP55412_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
    纯化方法
    Purified
  • 应用备注
    Each Investigator should determine their own optimal working dilution for specific applications.
    限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    浓度
    1 mg/mL
    缓冲液
    Final peptide concentration is 1 mg/mL in PBS.
    注意事项
    Avoid repeated freeze-thaw cycles.
    储存条件
    -20 °C
    储存方法
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • 抗原
    FGF13 (Fibroblast Growth Factor 13 (FGF13))
    别名
    FGF13 Peptide, fgf2 Peptide, fhf2 Peptide, fgf13 Peptide, FGF-13 Peptide, xFGF13 Peptide, FGF2 Peptide, FHF-2 Peptide, FHF2 Peptide, Fhf2 Peptide, zgc:101784 Peptide, fibroblast growth factor 13 Peptide, fibroblast growth factor 13 L homeolog Peptide, fibroblast growth factor 13a Peptide, FGF13 Peptide, fgf13 Peptide, fgf13.L Peptide, Fgf13 Peptide, fgf13a Peptide
    背景
    FGF13 is probably involved in nervous system development and function.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 gene is located to a region associated with Borjeson-Forssman-Lehmann syndrome (BFLS), a syndromal X-linked mental retardation, which suggests it may be a candidate gene for familial cases of the BFL syndrome. The function of this gene has not yet been determined. Two alternatively spliced transcripts encoding different isoforms have been described for this gene.

    Alias Symbols: FGF2, FHF2, FHF-2, FGF-13

    Protein Interaction Partner: FGF13,SCN8A,MAPK8IP2

    Protein Size: 245
    分子量
    27 kDa
    基因ID
    2258
    NCBI登录号
    NM_004114, NP_004105
    UniProt
    Q92913
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