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- 爱必信(absin)
- abs158141
- 上海
- 2025年07月14日
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- 详细信息
- 文献和实验
- 技术资料
- 抗体名：
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- 抗体英文名：
,FOXP3; IPEX; JM2; Forkhead box protein P3; Scurfin
- 靶点：
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- 浓度：
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- 应用范围：
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- 宿主：
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- 适应物种：
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- 保质期：
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- 抗原来源：
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- 目录编号：
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- 级别：
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- 库存：
99
- 供应商：
爱必信(上海)生物科技有限公司
- 标记物：
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- 克隆性：
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- 保存条件：
Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
- 形态：
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- 亚型：
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- 免疫原：
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- 规格：
100ul
| 概述 | |
| 别名 | FOXP3; IPEX; JM2; Forkhead box protein P3; Scurfin |
| 宿主 | Mouse |
| 反应种属 | Transfected |
| 应用 | WB: 1/500-1/1000, IF: 1/50-1/200 |
| 分子量 | Detects a band of approximately 47 kD(Predicted molecular weight: 47 kD) Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors. |
| 免疫原 | Purified recombinant human FOXP3 protein fragments expressed in E.coli. |
| 性能 | |
| 形式 | Monoclonal Antibody |
| 纯化方法 | Affinity Purified |
| 克隆号 | 7H9 |
| 同种型 | IgG1 |
| 储存/保存方法 | Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. |
| 存储溶液 | Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide, pH 7.3. |
| 修饰 | Unmodified |
| 靶标 | |
| 背景说明 | Defects in FOXP3 are the cause of immunodeficiency polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) [MIM:304790]; also known as X-linked autoimmunity-immunodeficiency syndrome. IPEX is characterized by neonatal onset insulin-dependent diabetes mellitus, infections, secretory diarrhea, trombocytopenia, anemia and eczema. It is usually lethal in infancy. |
| UniProt | Q9BZS1 |
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文献和实验(adjust pH to 7.8 with Binding buffer; red color) to the Protein A column.Mouse antibodies of the IgG1 subclass do not have a high affinity for protein A. Purification on protein A beads using standard conditions will yield approximately 1/10
In Vivo Depletion of FoxP3+ Tregs Using the DEREG Mouse Model
was precluded due to the lack of appropriate markers. Only after the discovery of Foxp3 as a Treg-specific transcription factor, was the development of Treg-specific mouse models feasible. We generated DEREG mice (DEpletion of REGulatory T cells), a BAC
. Mice and human with Foxp3 mutations are severely impaired in Treg cell generation and develop lethal autoimmune diseases. We combined chromatin immuno-precipitation and mouse whole genome tiling array profiling (ChIP-on-Chip) to identify the direct
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