FXR2抗体FXR2一抗抗体Human fragile X
mental retardation syndrome related protein FXR2 mRNA complete cds antibody抗体FXR2 Antibody抗体- ￥3900
- CUSABIO
- CN
- CSB-PA009088GA01HU
- 2025年07月10日
- ELISA,WB
- Rabbit
- Human,Mouse,Rat
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
Human FXR2
- 亚型：
IgG
- 形态：
Liquid
- 保存条件：
Upon receipt, store at -20℃ or -80℃. Avoid repeated freeze.
- 克隆性：
/
- 标记物：
/
- 适应物种：
Human,Mouse,Rat
- 保质期：
6个月
- 抗原来源：
Homo sapiens (Human)
- 目录编号：
P51116
- 级别：
优
- 库存：
200
- 供应商：
武汉华美生物工程有限公司
- 宿主：
Rabbit
- 应用范围：
ELISA,WB
- 浓度：
>95%,Antigen Affinity Purified
- 靶点：
FXR2
- 抗体英文名：
FXR2 Antibody
- 抗体名：
Human fragile X mental retardation syndrome related protein FXR2 mRNA complete cds antibody
- 规格：
100μl
保存缓冲液
PBS with 0.1% Sodium Azide, 50% Glycerol, pH 7.3. -20℃, Avoid freeze / thaw cycles.功能
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文献和实验Identification of Messenger RNAs and MicroRNAs Associated With Fragile X Mental Retardation Protein
Fragile X syndrome, a common form of inherited mental retardation, is caused by the loss of the Fragile X mental retardation protein (FMRP). FMRP, which may regulate translation in neurons, not only associates with specific messenger RNAs
Protein Components of the microRNA Pathway and Human Diseases
, Exportin-5 (Exp-5), TAR RNA binding protein (TRBP) and fragile X mental retardation protein (FMRP), are each related, in various ways, to specific genetic diseases.
Detection of FMR1 Trinucleotide Repeat Expansion Mutations Using Southern Blot and PCR Methodologies
Fragile X syndrome, caused by the loss or diminution of the FMR1 (FRAXA - chromosomal locus Xq27.3) encoded protein, FMRP, results in mild to moderate mental retardation as its hallmark. Patients with the syndrome often vary dramatically
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