- ￥2300
- AntibodySystem
- FMK16410
- 2025年07月14日
- FCM, IF, IHC
- Armenian Hamster
- Mouse
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- 详细信息
- 文献和实验
- 技术资料
- 抗体名：
Anti-Mouse TCR γ/δ Antibody (UC7-13D5)
- 抗体英文名：
Anti-Mouse TCR γ/δ Antibody (UC7-13D5)
- 浓度：
1 mg/ml
- 应用范围：
FCM, IF, IHC
- 宿主：
Armenian Hamster
- 适应物种：
Mouse
- 保质期：
1 year
- 级别：
科研级
- 库存：
999
- 供应商：
AntibodySystem
- 克隆性：
Monoclonal
- 亚型：
IgG
- 规格：
100ug
| 宿主 | Armenian Hamster |
| 偶联物 | Unconjugated |
| 种属反应性 | Mouse |
| 状态 | Liquid |
| 保存溶液 | 0.01M PBS, pH 7.4. |
| 浓度 | 1 mg/ml |
| 纯度 | >95% as determined by SDS-PAGE. |
| 克隆类型 | Monoclonal |
| 同种型 | IgG |
| 应用 | FCM, IF, IHC |
| 靶标 | TCR-γ/δ, γ/δ TCR |
| 纯化方式 | Protein A/G purified from cell culture supernatant. |
| 内毒素水平 | Please contact with the lab for this information. |
| 稳定性和存储 | Use a manual defrost freezer and avoid repeated freeze-thaw cycles. Store at 4°C short term (1-2 weeks). Store at -20°C 12 months. Store at -80°C long term. |
| 克隆号 | UC7-13D5 |
| 备注 | For research use only. |
Our products are designed for various research areas, supporting studies on 48 types of viruses, superbugs, parasites, cancer, Alzheimer's disease, Parkinson's disease, allergic responses, immune suppression, and immune activation.
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文献和实验【进展|热点】Immunity: γδ T细胞抑制调节性T细胞
γδ T细胞抑制调节性T细胞 文章出处：γδ T Cells Enhance Autoimmunity by Restraining Regulatory T Cell Responses via an Interleukin-23-Dependent Mechanism. Immunity. 2010. 33:351-363 主要内容： T细胞根据其TCR链的不同可以分为αβ T细胞和γδ T细胞两类，前者是经典的T细胞，我们常规提到的T细胞指的就是αβ T细胞。γδ
Purification of Immature CD4+CD8+ Thymocytes by Panning with Anti-CD8 Antibody
by their expression of the coreceptor proteins CD4 and CD8 and their surface density of aβ T cell receptors (αβ TCR), ( 1 ). Three major subpopulations of T cells exist within the thymus that exemplify the progression of thymocytes along the CD4/CD8 developmental
Differentiation of Mouse Thymocytes in Fetal Thymus Organ Culture
.g., CD4+ T cells vs CD8+ T cells, and TCR-αβ+ T cells vs TCR-γδ+ T cells, 2. clonal selection, e.g., positive selection of useful T-cell clones and negative selection of harmful T-cell clones
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