- ￥2500 - 3600
- CUSABIO
- 3.9pg/mL
- 武汉
- CSB-EL008756HU
- 2025年12月31日
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- 详细信息
- 文献和实验
- 技术资料
- 供应商：
武汉益普生物科技有限公司
- 检测范围：
3.9pg/mL
- 检测方法：
Sandwich
- 应用：
Signal Transduction
- 适应物种：
Homo sapiens (Human)
- 样本：
serum, plasma, tissue homogenates
- 规格：
96T/48T
| 规格： | 96T | 产品价格： | ￥3600.0 |
|---|---|---|---|
| 规格： | 48T | 产品价格： | ￥2500.0 |
| Product Name |
Human Fragile X mental retardation 1 protein(FMR1) ELISA Kit |
| Chinese Name |
人脆性X智力低下蛋白1（FMR1）ELISA Kit |
| Code |
CSB-EL008756HU |
| Alternative Names |
FMR 1 ELISA Kit; Fmr1 ELISA Kit; Fmr1 gene ELISA Kit; FMR1_HUMAN ELISA Kit; FMRP ELISA Kit; Fragile X mental retardation 1 ELISA Kit; Fragile X mental retardation 1 protein ELISA Kit; Fragile X mental retardation protein 1 ELISA Kit; Fragile X mental retardation protein ELISA Kit; fragile X mental retardation syndrome-related protein 1 ELISA Kit; fragile X mental retardation; autosomal homolog 1 ELISA Kit; FRAXA ELISA Kit; fxr1 ELISA Kit; MGC87458 ELISA Kit; POF ELISA Kit; POF1 ELISA Kit; Protein FMR-1 ELISA Kit; Protein FMR1 ELISA Kit; wu:fb16f11 ELISA Kit; wu:fd18c10 ELISA Kit; zgc:66226 ELISA Kit |
| Target Name |
fragile X mental retardation 1 |
| Abbreviation |
FMR1 |
| Uniprot No. |
Q06787 |
| Species |
Homo sapiens (Human) |
| Sample Types |
serum, plasma, tissue homogenates |
| Detection Range |
15.6pg/mL-1000pg/mL |
| Sensitivity |
3.9pg/mL |
| Assay Principle |
quantitative |
| Measurement |
Sandwich |
| Assay Time |
1-5h |
| Sample Volume |
50-100ul |
| Detection Wavelength |
450nm |
| Research Area |
Signal Transduction |
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文献和实验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
Characterizing Social Behavior in Genetically Targeted Mouse Models of Brain Disorders
Fragile X syndrome, the leading inherited cause of mental retardation and autism spectrum disorders worldwide, is caused by a tandem repeat expansion in the FMR1 (fragile X mental retardation 1) gene. It presents
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