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FGF13 抗体

FGF13 适用: 人, 大鼠, 小鼠 WB, IHC, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN5697729
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), Immunohistochemistry (IHC), ELISA
    免疫原
    fibroblast growth factor 13
    亚型
    IgG
    Top Product
    Discover our top product FGF13 Primary Antibody
  • 应用备注
    Optimal working dilution should be determined by the investigator.
    说明

    Transfected HEK-293 cells were subjected to SDS PAGE followed by western blot with FNab03090( FGF13 Antibody) at dilution of 1:1000

    限制
    仅限研究用
  • 缓冲液
    PBS with 0.02 % sodium azide and 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.
    注意事项
    Avoid repeated freeze / thaw cycles.
    储存条件
    -20 °C
    有效期
    12 months
  • 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
    Synonyms:FHF2 Background: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
    28-30 kDa
    基因ID
    2258
    UniProt
    Q92913
    途径
    Regulation of Cell Size
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