- ￥2050 - 3180
- immunoclone、ABCAM、BD、SANTA
- 中国/美国/德国
- IC233335
- 2025年07月11日
- WB,
- Mouse
- Human,
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- 详细信息
- 文献和实验
- 技术资料
- 亚型：
IgG
- 形态：
Lyophilized or Liquid
- 保存条件：
-20℃
- 克隆性：
多克隆
- 适应物种：
Human,
- 宿主：
Mouse
- 应用范围：
WB,
- 浓度：
1mg/1ml
- 抗体英文名：
FMR1 Antibody
- 抗体名：
FMR1 Antibody
- 规格：
100ug
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文献和实验The CGG Repeat and the FMR1 Gene
This review intends to provide the different DNA methods for diagnosis of the repeat in the FMR1 gene. The two DNA methods to determine the CGG repeat size are Southern blot hybridization and the polymerase chain reaction (PCR), including
Epigenetic Modifications of the FMR1 Gene
The fragile X syndrome (FXS), the most common cause of heritable intellectual disability, is caused by expansion of a CGG repeat located at the 5′ UTR of the FMR1 gene and subsequent epigenetic modifications of its promoter. Epigenetic
Development and Characterization of Antibodies that Immunoprecipitate the FMR1 Protein
The ability to generate antibodies that recognize a given protein relies on that protein’s “antigenicity”, i.e., its ability to appear foreign to the host immune system. Thus, proteins that are highly conserved among species are often poor
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