重组抗小鼠CD3e单抗(KT3) | Syd Labs PA007521.r2a
体内实验级重组抗小鼠CD3e单抗(克隆号:KT3,货号:PA007521.r2a),大鼠IgG2a Kappa 是用哺乳动物细胞生产的重组抗体,适用于体外和体内研究,纯度>95%。其不变区为大鼠IgG2a kappa (rIgG2a或r2a),可与重组大鼠IgG2a同型对照抗体配套使用。样品制备条件和最佳样品稀释度应由研究人员通过实验确定。
产品参数
| 货号 | PA007521.r2a |
|---|---|
| 产品名称 | 重组抗小鼠CD3e单抗(KT3) | Syd Labs PA007521.r2a |
| 英文名 | In Vivo Grade Recombinant Anti-mouse CD3e Monoclonal Antibody (Clone: KT3), Rat IgG2a Kappa |
| 供货商名称 | Syd Labs, Inc. |
| 品牌名 | Syd Labs |
| 别称 | 分化簇3,CD3D,CD3E,CD3G |
| 概述 | Syd Labs提供重组大鼠IgG2a同型对照抗体。样品制备条件和最佳样品稀释度应由研究人员通过实验确定。 |
| 克隆号 | KT3 |
| 同种型 | 大鼠 IgG2a Kappa |
| 来源 | 抗小鼠CD3e单克隆抗体(克隆:KT3)在哺乳动物细胞中产生 |
| 特异性 | 体内实验级重组大鼠单克隆抗体(克隆:KT3)特异性结合小鼠T细胞受体CD3e |
| 抗体形式 | 0.2微米过滤溶液,pH 7.4,无稳定剂或防腐剂 |
| 内毒素 | 根据 LAL 方法,≤1 EU每1mg 蛋白质 |
| 纯度 | >95%(在还原条件下通过SDS-PAGE测定) |
| 运输 | 体内实验级重组抗小鼠CD3e单克隆抗体,大鼠IgG2a Kappa(克隆号KT3)用冰袋运输。收到后,请立即将其存放在下面建议的温度下。 |
| 稳定性与存储 | 使用手动除霜冰箱并避免重复冻融循环。 自收到之日起 1 个月,保存在2 至 8°C。 自收到之日起12个月,保存在-20 至 -70°C。 |
| 注意事项 | PA007521.r2a Syd Labs:体内实验级重组抗小鼠CD3e大鼠IgG2a单克隆抗体(克隆号KT3) 是用哺乳动物细胞生产的重组抗体,可与重组大鼠IgG2a同型对照抗体配套使用。样品制备条件和最佳样品稀释度应由研究人员通过实验确定。 |
| 产品咨询 | Syd Labs在国内只通过代理商销售其产品,不做直销。终端用户咨询价格请联系Syd Labs中国代理商。 关于Syd Labs产品如果有任何技术或其它问题,欢迎随时联系Syd Labs国内市场推广合作伙伴:武汉多找找科技有限公司,企业微信:duozhaozhao2024 联系电话:18162581039(龙经理) |
| 应用详情 | ELISA,流式细胞术(FC),中和(neutralization),功能测定如生物分析 PK 和 ADA 测定,以及那些用于研究受小鼠CD3e蛋白影响的生物学途径的测定。 |
文献
PA007521.r2a:体内实验级重组抗小鼠CD3e单克隆抗体(克隆号KT3),大鼠IgG2a Kappa
体内实验级重组抗小鼠CD3e单克隆抗体(克隆号KT3,大鼠IgG2a Kappa)是针对小鼠T细胞受体(TCR)复合物核心亚基CD3ε(CD3 epsilon)的序列明确(sequence-defined)重组单克隆抗体。CD3ε链作为T细胞信号转导的关键组分,几乎表达于所有成熟T细胞及胸腺细胞表面,在T细胞激活、增殖及细胞因子释放中发挥核心作用。该重组抗小鼠CD3e单克隆抗体(克隆号KT3)采用先进的哺乳动物细胞重组表达系统生产,完整保留了大鼠KT3克隆特异性结合表位。相比易发生基因漂移、轻链污染与批次间波动的传统杂交瘤来源试剂,重组表达技术确保了批次间的高度一致性与序列保真度,为T细胞免疫学研究提供了高可靠性的科研保障。
在体内免疫学与肿瘤免疫治疗模型研究中,体内实验级重组抗小鼠CD3e单克隆抗体(克隆号KT3)既可用于体内T细胞强效激活与免疫应答诱导,也可用于特定方案下的体内T细胞清除(In Vivo T Cell Depletion)或免疫耐受调控。凭借大鼠IgG2a Kappa格式稳定的Fc段效应功能,该抗体能够高效介导靶向免疫调节。为确保动物活体注射的安全性和实验数据的准确性,该低内毒素重组抗小鼠CD3e抗体(克隆号KT3)经过严格的纯化工艺,内毒素水平低于1 EU/mg,配方完全无叠氮化钠与防腐剂,有效规避了全身性非特异性炎症干扰,为移植排斥、自身免疫病及肿瘤免疫机制研究提供干净、符合顶级期刊发表标准的数据支持。
抗小鼠 CD3ε 单克隆抗体(克隆号:KT3)参考文献:
Thawer, S. G., et al. Mucosal Immunol. 2014 Mar;7(2):239-48. PMID: 23778354
“Rat anti-mouse CD3 (KT3) was purchased from Abcam. …Data were expressed as mean ± s.d. and analyzed using one-tailed Mann-Whitney nonparametric T test with a 95% confidence interval. …The work presented was funded by National Research Foundation, Medical Research Council (South Africa), International Centre for Genetic Engineering and Biotechnology, Worldwide Universities Network, and Claude Leon Foundation. …Whole lung was removed from individual mice, finely cut, and digested in Iscove’s modified Eagle medium (Invitrogen, Carlsbad, CA) containing 50 U ml⁻¹ collagenase type I (Invitrogen) and 13 µg ml⁻¹ DNase (Roche, Carlsbad, CA) at 37 °C for 90 min. …Lung worm burdens were quantified as previously described by finely cutting the lung, placing on sterile gauze, and suspending them in a 50-ml centrifuge tube containing phosphate-buffered saline at 37 °C for at least 3 h.”
Sathe, P., et al. Immunity. 2014 Jul 17;41(1):104-15. PMID: 25035955
“The mAb hybridoma clones used were CD2 (RM2-1), CD3 (KT3), CD8 (YTS169.4 or 53-6.7), CD19 (1D3) CD45R (RA36B2), CD11b (M1/70), TER119 (TER119), Ly6G (1A8), CD45.1 (A20.1), CD45.2 (S450-15.2), CD11c (N418), F4/80 (F4/80), CD34 (RAM34), sca-1 (E13 161-7), c-kit (ACK2), flt3 (A2F10.1), CD16/32 (2.4G2), and M-CSFR (AFS98). …Mice were 6-12 weeks of age. Unless otherwise indicated, experiments were performed using C57BL/6J Wehi (CD45.2) mice. …Mice were bred under specific-pathogen-free conditions at the Walter and Eliza Hall Institute; breeding and procedures were approved by the Animal Ethics Committee, WEHI. For analysis of precursors in FL-deficient mice, BM was extracted from C57BL/6-flt3l⁻/⁻ (FL⁻/⁻) mice from the University of Western Australia Animal Care Facility under the guidelines of the UWA Animal Ethics Office. …Erythrocytes, dead cells, and very dense cells, were eliminated from BM cell suspensions by centrifugation in Nycodenz (Nycomed Pharma) medium (1.086 g/cm³, 4°C, mouse osmolarity). …Progenitors were isolated from CX3CR1-GFP or CD45.1 BM and 5 × 10⁴-2 × 10⁵ cells transferred intravenously into lethally irradiated CD45.2 recipients.”
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