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FGF13 抗体

This anti-FGF13 antibody is a 兔 多克隆 antibody detecting FGF13 in IHC 和 ELISA. Suitable for 人, 大鼠 和 小鼠.
产品编号 ABIN7244969
发货至: 中国
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中国
北京 101111
No. 88 KeChuang 6th Street
Beijing Economic Technological Development Area
Room 801-803
4A Biotech Co.,Ltd.
Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for FGF13 抗体 (ABIN7244969)

抗原

See all FGF13 抗体
FGF13 (Fibroblast Growth Factor 13 (FGF13))

适用

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  • 13
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  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
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人, 大鼠, 小鼠

宿主

  • 50
  • 42
  • 1

克隆类型

  • 54
  • 39
多克隆

标记

  • 40
  • 8
  • 8
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This FGF13 antibody is un-conjugated

应用范围

  • 56
  • 37
  • 34
  • 25
  • 15
  • 13
  • 13
  • 10
  • 4
  • 3
  • 2
  • 1
Immunohistochemistry (IHC), ELISA
  • 产品特性

    Polyclonal Antibody

    纯化方法

    Antigen affinity purification

    免疫原

    Synthetic peptide of human FGF13

    亚型

    IgG
  • 应用备注

    IHC 1:40-1:200, ELISA 1:5000-1:10000

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1.26 mg/mL

    缓冲液

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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

    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.

    UniProt

    Q92913

    途径

    Regulation of Cell Size
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