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- PVT10261
- 2025年07月16日
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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
负20摄氏度
- 保质期：
3个月
- 英文名：
pDsRed2-FMR1
- 库存：
50
- 供应商：
LSMBIO
- 规格：
2ug
pDsRed2-FMR1/ pDsRed2-FMR1璐ㄧ矑
pDsRed2-FMR1
Catalog No. PVT10261
Packing 2ug
Function ORF expression plasmid
Resistance Kan
Screen /
Strain DH5alpha
Culture temperature 37degrees centigrade
Replicon
Copy
Promoter
Induction
Forward primer
Reverse primer
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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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