电话:
400-7060-959
传真:
+86 10 56315212-8813
电子邮件:
orders@antibodies-online.cn

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

FGF13 适用: 人 宿主: 合成 BP, WB
产品编号 ABIN976829
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)
    序列
    PKPLKVAMYK EPSLHDLTEF SRSGSGTPTK SRSVSGVLNG GKSMSHNEST
    产品特性
    This is a synthetic peptide designed for use in combination with anti-FGF13 Antibody(ARP55413_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
    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 in a region on chromosome X, which is associated with Borjeson-Forssman-Lehmann syndrome (BFLS), making it a possible candidate gene for familial cases of the BFLS, and for other syndromal and nonspecific forms of X-linked mental retardation mapping to this region. Alternative splicing of this gene at the 5' end results in several transcript variants encoding different isoforms with different N-termini.

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

    Protein Interaction Partner: FGF13,SCN8A,MAPK8IP2

    Protein Size: 192
    分子量
    21 kDa
    基因ID
    2258
    NCBI登录号
    NM_033642, NP_378668
    UniProt
    Q92913
You are here:
客服