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NOG 抗体

This anti-NOG antibody is a 兔 多克隆 antibody detecting NOG in IHC 和 ELISA. Suitable for 人 和 小鼠.
产品编号 ABIN7244756
发货至: 中国

Quick Overview for NOG 抗体 (ABIN7244756)

抗原

See all NOG 抗体
NOG (Noggin (NOG))

适用

  • 67
  • 45
  • 32
  • 9
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  • 1
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  • 1
人, 小鼠

宿主

  • 96
  • 18
  • 1

克隆类型

  • 99
  • 16
多克隆

标记

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  • 7
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This NOG antibody is un-conjugated

应用范围

  • 96
  • 51
  • 37
  • 28
  • 26
  • 14
  • 13
  • 13
  • 6
  • 6
  • 5
  • 3
  • 1
Immunohistochemistry (IHC), ELISA
  • 产品特性

    Polyclonal Antibody

    纯化方法

    Antigen affinity purification

    免疫原

    Synthetic peptide of human NOG

    亚型

    IgG
  • 应用备注

    IHC 1:25-1:100, ELISA 1:5000-1:10000

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1.9 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

    NOG (Noggin (NOG))

    别名

    NOG

    背景

    NOG (Noggin) is a Protein Coding gene. Diseases associated with NOG include Tarsal-Carpal Coalition Syndrome and Brachydactyly, Type B2. Among its related pathways are Mesodermal Commitment Pathway and Differentiation Pathway. GO annotations related to this gene include protein homodimerization activity and cytokine binding.The secreted polypeptide, encoded by this gene, binds and inactivates members of the transforming growth factor-beta (TGF-beta) superfamily signaling proteins, such as bone morphogenetic protein-4 (BMP4). The protein appears to have pleiotropic effect, both early in development as well as in later stages. It was originally isolated from Xenopus based on its ability to restore normal dorsal-ventral body axis in embryos that had been artificially ventralized by UV treatment. The results of the mouse knockout of the ortholog suggest that it is involved in numerous developmental processes, such as neural tube fusion and joint formation. Recently, several dominant human NOG mutations in unrelated families with proximal symphalangism (SYM1) and multiple synostoses syndrome (SYNS1) were identified, both SYM1 and SYNS1 have multiple joint fusion as their principal feature, and map to the same region (17q22) as this gene.

    UniProt

    Q13253

    途径

    Stem Cell Maintenance, Tube Formation
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