电话:
+86 (0512) 65829739
传真:
+86 (010) 6788 5057
电子邮件:
orders@antibodies-online.cn

GDF6 抗体 (N-Term)

This anti-GDF6 antibody is a 兔 多克隆 antibody detecting GDF6 in WB, FACS 和 IHC (p). Suitable for 小鼠.
产品编号 ABIN655618
发货至: 中国

Quick Overview for GDF6 抗体 (N-Term) (ABIN655618)

抗原

See all GDF6 抗体
GDF6 (Growth Differentiation Factor 6 (GDF6))

适用

  • 37
  • 21
  • 15
  • 1
  • 1
小鼠

宿主

  • 40
  • 2

克隆类型

  • 40
  • 2
多克隆

标记

  • 22
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This GDF6 antibody is un-conjugated

应用范围

  • 36
  • 13
  • 13
  • 13
  • 8
  • 8
  • 6
  • 6
  • 6
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

克隆位点

RB14527
  • 抗原表位

    • 15
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 31-59, N-Term

    纯化方法

    This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.

    免疫原

    This GDF6 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 31-59 amino acids from the N-terminal region of human GDF6.

    亚型

    Ig Fraction
  • 应用备注

    WB: 1:1000. IHC-P: 1:50~100. FC: 1:10~50

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    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

    4 °C,-20 °C

    储存方法

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    有效期

    6 months
  • 抗原

    GDF6 (Growth Differentiation Factor 6 (GDF6))

    别名

    GDF6

    背景

    This gene encodes a member of the bone morphogenetic protein (BMP) family and the TGF-beta superfamily of secreted signaling molecules. It is required for normal formation of some bones and joints in the limbs, skull, and axial skeleton. Mutations in this gene result in colobomata, which are congenital abnormalities in ocular development, and in Klippel-Feil syndrome (KFS), which is a congenital disorder of spinal segmentation.

    分子量

    50662

    基因ID

    392255

    NCBI登录号

    NP_001001557

    UniProt

    Q6KF10
You are here:
Chat with us!