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FGF13 抗体

FGF13 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN2854901
发货至: 中国
  • 抗原 See all FGF13 抗体
    FGF13 (Fibroblast Growth Factor 13 (FGF13))
    适用
    • 58
    • 13
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    • 3
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    • 2
    • 1
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    宿主
    • 44
    • 20
    • 1
    克隆类型
    • 48
    • 17
    多克隆
    标记
    • 30
    • 7
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    • 1
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    This FGF13 antibody is un-conjugated
    应用范围
    • 43
    • 31
    • 18
    • 16
    • 14
    • 13
    • 13
    • 5
    • 5
    • 3
    • 3
    • 2
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    交叉反应
    人, 小鼠, 大鼠
    产品特性
    Rabbit Polyclonal antibody to FGF13 (fibroblast growth factor 13)
    FGF13 antibody
    纯化方法
    Purified by antigen-affinity chromatography.
    免疫原
    Recombinant protein encompassing a sequence within the center region of human FGF13. The exact sequence is proprietary.
    亚型
    IgG
  • 应用备注
    WB: 1:500-1:3000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
    说明

    Validation: Comparison

    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 mg/mL
    缓冲液
    1XPBS ( pH 7), 1 % BSA, 20 % Glycerol, 0.01 % Thimerosal
    储存液
    Thimerosal (Merthiolate)
    注意事项
    This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    储存条件
    4 °C,-20 °C
    储存方法
    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • 抗原
    FGF13 (Fibroblast Growth Factor 13 (FGF13))
    别名
    fibroblast growth factor 13 (FGF13 产品)
    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
    28 kDa
    基因ID
    2258
    UniProt
    Q92913
    途径
    Regulation of Cell Size
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