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FGF13 抗体

FGF13 适用: 人, 大鼠, 小鼠 WB, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN2459900
发货至: 中国
  • 抗原 See all FGF13 抗体
    FGF13 (Fibroblast Growth Factor 13 (FGF13))
    适用
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    人, 大鼠, 小鼠
    宿主
    • 45
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    克隆类型
    • 49
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    多克隆
    标记
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    This FGF13 antibody is un-conjugated
    应用范围
    • 44
    • 31
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    Western Blotting (WB), ELISA
    纯化方法
    Antibody is purified by peptide affinity chromatography method.
    免疫原
    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human FGF13.
    Top Product
    Discover our top product FGF13 Primary Antibody
  • 应用备注
    FGF13 antibody can be used for detection of FGF13 by ELISA at 1:62500. FGF13 antibody can be used for detection of FGF13 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
    限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
    浓度
    1 mg/mL
    缓冲液
    Antibody is lyophilized in PBS buffer with 2 % sucrose.
    注意事项
    As with any antibody avoid repeat freeze-thaw cycles.
    储存条件
    4 °C/-20 °C
    储存方法
    For short periods of storage (days) store at 4 °C. For longer periods of storage, store FGF13 antibody at -20 °C.
  • 抗原
    FGF13 (Fibroblast Growth Factor 13 (FGF13))
    别名
    FGF13 (FGF13 产品)
    别名
    FGF13 antibody, fgf2 antibody, fhf2 antibody, fgf13 antibody, FGF-13 antibody, xFGF13 antibody, FGF2 antibody, FHF-2 antibody, FHF2 antibody, Fhf2 antibody, zgc:101784 antibody, fibroblast growth factor 13 antibody, fibroblast growth factor 13 L homeolog antibody, fibroblast growth factor 13a antibody, FGF13 antibody, fgf13 antibody, fgf13.L antibody, Fgf13 antibody, fgf13a antibody
    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.
    分子量
    27 kDa
    基因ID
    2258
    NCBI登录号
    NP_004105
    UniProt
    Q92913
    途径
    Regulation of Cell Size
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