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FGF13 抗体

FGF13 适用: 人, 大鼠, 小鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7263929
发货至: 中国
  • 抗原 See all FGF13 抗体
    FGF13 (Fibroblast Growth Factor 13 (FGF13))
    适用
    • 58
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    • 11
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    • 3
    • 3
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    • 2
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    人, 大鼠, 小鼠
    宿主
    • 44
    • 20
    • 1
    克隆类型
    • 48
    • 17
    多克隆
    标记
    • 30
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    • 3
    • 1
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    This FGF13 antibody is un-conjugated
    应用范围
    • 43
    • 30
    • 18
    • 16
    • 14
    • 13
    • 13
    • 5
    • 5
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    • 2
    Western Blotting (WB), Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human FGF13 (NP_004105.1).
    亚型
    IgG
    Top Product
    Discover our top product FGF13 Primary Antibody
  • 应用备注
    WB 1:500-1:2000 IHC 1:50-1:200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 mg/mL
    缓冲液
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    储存液
    Sodium azide
    注意事项
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 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
    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.
    分子量

    Observed_MW: 28 kDa

    Calculated_MW: 21 kDa/22 kDa/25 kDa/27 kDa/28 kDa

    基因ID
    2258
    UniProt
    Q92913
    途径
    Regulation of Cell Size
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