重组抗小鼠TCR gamma/delta单抗(UC7-13D5) | Syd Labs PA007541.m1

重组抗小鼠TCR gamma/delta单抗(UC7-13D5) Syd Labs PA007541.m1 - 武汉多找找科技

重组抗小鼠TCR gamma/delta单抗(UC7-13D5) | Syd Labs PA007541.m1

In stock

一键复制

体内实验级重组抗小鼠TCR gamma/delta单抗(克隆号:UC7-13D5,货号:PA007541.m1)小鼠IgG1 Kappa 是用哺乳动物细胞生产的重组抗体,纯度>95%,适用于体外和体内研究,比如体内TCRγ/δ中和。Syd Labs PA007541.m1抗小鼠TCR gamma/delta抗体不变区为小鼠Mouse IgG1 Kappa (mIgG1或m1),可与重组小鼠IgG1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 PA007541.m1
产品名称重组抗小鼠TCR gamma/delta单抗(UC7-13D5) | Syd Labs PA007541.m1
英文名 In Vivo Grade Recombinant Anti-mouse TCR gamma/delta Monoclonal Antibody (Clone: UC7-13D5), Mouse IgG1 Kappa
供货商名称 Syd Labs, Inc.
品牌名 Syd Labs
别称 TCR gamma, TCRG, TCR delta, TCRD, TCRDV1
概述 Syd Labs 重组抗小鼠TCR gamma/delta单克隆抗体(克隆:UC7-13D5) 是用哺乳动物细胞生产的重组抗体,可与重组小鼠IgG1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。
克隆号 UC7-13D5
同种型 小鼠 IgG1 Kappa
特异性 体内实验级重组小鼠单克隆抗体 (克隆:UC7-13D5) 特异性与小鼠 TCR gamma/delta 结合
抗体形式 0.2 μM过滤溶液,pH 7.4,不含稳定剂或防腐剂
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TCR gamma/delta单克隆抗体(克隆号UC7-13D5),小鼠IgG1 Kappa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 PA007541.m1 Syd Labs:抗小鼠TCR gamma/delta单克隆抗体是用哺乳动物细胞生产的,可与重组小鼠IgG1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、中和、功能测定,如生物分析PK和ADA测定,以及用于研究受小鼠TCR gamma/delta蛋白影响的生物途径的测定

文献

PA007541.m1: Syd Labs体内实验级重组抗小鼠TCR gamma/delta单克隆抗体(克隆号UC7-13D5),小鼠IgG1Kappa(In Vivo Grade Recombinant Anti-mouse TCR gamma/delta Monoclonal Antibody (Clone: UC7-13D5), Mouse IgG1 Kappa)

体内实验级重组抗小鼠TCR gamma/delta单克隆抗体(克隆号UC7-13D5)是专为阻断和检测小鼠γδ T细胞表面TCR γ/δ受体复合体设计的特异性免疫试剂。γδ T细胞作为连接固有免疫与适应性免疫的关键淋巴细胞,在早期抗感染、肿瘤免疫监视及黏膜免疫屏障维护中扮演重要角色。克隆号UC7-13D5抗体能特异性识别小鼠TCR γ/δ异二聚体,被广泛应用于流式细胞术(FC)、免疫组化(IHC)、体外激活以及体内(In Vivo)γδ T细胞功能耗竭/清除(Depletion)与免疫调节机制研究。

作为高品质的体内实验级重组抗小鼠TCR gamma/delta单克隆抗体(克隆号UC7-13D5),该产品采用重组表达技术和小鼠IgG1 Kappa(或IgG2a Kappa工程化亚型)优化构建,彻底消除了传统杂交瘤表达中的批次间差异,并具备极高的特异性与结合活性。产品严格执行低内毒素(<1 EU/mg)与无叠氮化钠防腐剂标准,可有效避免动物体内非特异性炎症反应与细胞毒性,完全满足长期动物体内实验(In Vivo)、肿瘤免疫疗法开发及自身免疫性疾病模型探究的高标准要求。

抗小鼠TCR gamma/delta抗体(UC7-13D5)部分参考文献:

1. IL17 Promotes Mammary Tumor Progression by Changing the Behavior of Tumor Cells and Eliciting Tumorigenic Neutrophils Recruitment.

Benevides, L., et al. Cancer Res. 2015. PMID: 26208902

“We found that CD3+CD4+, CD3+CD8+, and CD3+γδ+ T cells produced IL17A and IFN-γ at all assessed points. …In particular, we observed an increase in the number of IL17A-producing CD3+CD4+ and TCRγδ+ T cells at 25 and 35 dpi. …For T-cell analysis, antibodies to the following mouse proteins were obtained: CD3 (145-2C11), CD4 (RM4-5), CD8 (53-6.7), TCR γδ (UC7-13D5), IL17A (TC11-18H10), and IFN-γ (XMG1.2).”

2. Thy1+ NK cells from vaccinia virus-primed mice confer protection against vaccinia virus challenge in the absence of adaptive lymphocytes.

Gillard, G. O., et al. PLoS Pathog. 2011. PMID: 21829360

“Ten days prior to a secondary vaccinia virus challenge we began administering isotype control antibodies or a cocktail of T cell-depleting monoclonal antibodies (clones GK1.5 (αCD4), H57-597 (αTCRαβ), and UC7-13D5 (αTCRγδ) ip) to groups of naïve and primed animals. …The efficiency of T cell depletion was monitored by flow cytometric analysis of peripheral blood stained with a panel of monoclonal antibodies, including antibodies specific for CD3, TCRαβ, TCRγδ, and NK1.1. …Very few of those cells that fall within the CD3+ gate in the depleted mice showed staining for TCRαβ, TCRγδ, or CD8α.”

3. Murine and bovine γδ T cells enhance innate immunity against Brucella abortus infections.

Skyberg, J. A., et al. PLoS One. 2011. PMID: 21765931

“Third panel from top, cells were gated on γδ T cells (CD3+/TCRγδ+) and assayed for IFN-γ production. …γδ T cells were found to be the major producer of IL-17 during infection and were also found to produce IFN-γ. …Neutralization of γδ T cells enhanced the susceptibility of both wt and IL-17R-/- γδ-/- mice, and IL-17 receptor deficiency did not impact splenomegaly, nor tissue colonization by B. abortus. …Deficiency of either IFN-γ or γδ T cells enhanced susceptibility to colonization by ~10-fold at one-week post-infection.”