抗小鼠CD8b单克隆抗体(克隆号YTS 156.7),体内实验级重组,大鼠IgG2b Kappa | Syd Labs PA007382.r2b

抗小鼠CD8b单克隆抗体(克隆号YTS 156.7),大鼠IgG2b Kappa,体内实验级重组 | Syd Labs PA007382.r2b

抗小鼠CD8b单克隆抗体(克隆号YTS 156.7),体内实验级重组,大鼠IgG2b Kappa | Syd Labs PA007382.r2b

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体内实验级重组抗小鼠CD8b单克隆抗体,大鼠IgG2b Kappa(克隆号:YTS 156.7,货号:PA007382.r2b)是用哺乳动物细胞生产的重组抗体,从大鼠抗小鼠CD8b单克隆抗体(克隆号:YTS 156.7)可变区序列中提取,可用于蛋白质印迹、免疫组织化学 (IHC)、流式细胞术 (FC) 和体内CD8+T细胞耗竭(清除)等研究。Syd Labs PA007382.r2b不变区为大鼠IgG2b kappa (rIgG2b或r2b),可与重组大鼠IgG2b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。

货号 PA007382.r2b
产品名称抗小鼠CD8b单克隆抗体(克隆号YTS 156.7),体内实验级重组,大鼠IgG2b Kappa | Syd Labs PA007382.r2b
英文名 In vivo Grade Recombinant Anti-mouse CD8b Monoclonal Antibody, Rat IgG2b Kappa (Clone: YTS 156.7)
供货商名称 Syd Labs, Inc.
品牌名 Syd Labs
别称 CD8β,T细胞表面糖蛋白CD8β链,CD_抗原CD8b
概述 重组抗小鼠CD8b单克隆抗体是用哺乳动物细胞生产的重组抗体,从大鼠抗小鼠CD8b单克隆抗体(克隆号:YTS 156.7)可变区序列中提取的,适合体外和体内研究。
克隆号 YTS 156.7
同种型 大鼠IgG2b, kappa
特异性 CD8b
应用 蛋白质印迹、免疫组织化学(IHC)、流式细胞术(FC)和体内CD8+T细胞耗竭(清除)。
抗体形式 0.2 μM过滤溶液,1x PBS
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CD8b单克隆抗体,大鼠IgG2b Kappa(克隆号YTS 156.7)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。 如果保存在2 至 8°C,自收到之日起可保存1个月。 如果保存在-20 至 -70°C,自收到之日起可保存 12个月。
注意事项 PA007382.r2b Syd Labs重组抗小鼠CD8b单克隆抗体是用哺乳动物细胞生产的重组抗体,从大鼠抗小鼠CD8b单克隆抗体(克隆号:YTS 156.7)可变区序列中提取的,适合体外和体内研究。
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描述

PA007382.r2b: Syd Labs体内实验级重组抗小鼠CD8b单克隆抗体(克隆号YTS 156.7),大鼠IgG2b Kappa(In vivo Grade Recombinant Anti-mouse CD8b Monoclonal Antibody, Rat IgG2b Kappa (Clone: YTS 156.7)))

抗小鼠CD8b单抗(YTS 156.7)部分参考文献:

1. Structure, function, and immunomodulation of the CD8 co-receptor
Shreyaa Srinivasan,et al.Front Immunol. 2024.PMCID: PMC11381289
“Expressed on the surface of CD8+ T cells, the CD8 co-receptor is a key component of the T cells that contributes to antigen recognition, immune cell maturation, and immune cell signaling. While CD8 is widely recognized as a co-stimulatory molecule for conventional CD8+ αβ T cells, recent reports highlight its multifaceted role in both adaptive and innate immune responses. In this review, we discuss the utility of CD8 in relation to its immunomodulatory properties. We outline the unique structure and function of different CD8 domains (ectodomain, hinge, transmembrane, cytoplasmic tail) in the context of the distinct properties of CD8αα homodimers and CD8αβ heterodimers. We discuss CD8 features commonly used to construct chimeric antigen receptors for immunotherapy. We describe the molecular interactions of CD8 with classical MHC-I, non-classical MHCs, and Lck partners involved in T cell signaling. Engineered and naturally occurring CD8 mutations that alter immune responses are discussed. The applications of anti-CD8 monoclonal antibodies (mABs) that target CD8 are summarized. Finally, we examine the unique structure and function of several CD8/mAB complexes. Collectively, these findings reveal the promising immunomodulatory properties of CD8 and CD8 binding partners, not only to uncover basic immune system function, but to advance efforts towards translational research for targeted immunotherapy.”
2. Genetic and commensal induction of IL-18 drive intestinal epithelial MHCII via IFNγ
L. A. Van Der Kraak,et al.Mucosal Immunol. 2021.PMCID: PMC8562907
“Major Histocompatibility Complex Class II (MHCII) is dynamically expressed on intestinal epithelial cells (IECs) throughout the intestine, but its regulation remains poorly understood. We observed that spontaneous upregulation of IEC MHCII in locally-bred Rag1−/− mice correlated with serum Interleukin (IL)-18, was transferrable via cohousing to commercially-bred immunodeficient mice and could be inhibited by both IL-12 and IL-18 blockade. Overproduction of intestinal IL-18 due to an activating Nlrc4 mutation upregulated IEC MHCII via classical inflammasome machinery independently of immunodeficiency or dysbiosis. Immunodeficient dysbiosis increased Il18 transcription, which synergized with NLRC4 inflammasome activity to drive elevations in serum IL-18. This IL-18-MHCII axis was confirmed in several other models of intestinal and systemic inflammation. Elevated IL-18 reliably preceded MHCII upregulation, suggesting an indirect effect on IECs, and mice with IL-18 overproduction showed activation or expansion of type 1 lymphocytes. Interferon Gamma (IFNg) was uniquely able to upregulate IEC MHCII in enteroid cultures and was required for MHCII upregulation in several in vivo systems. Thus, we have linked intestinal dysbiosis, systemic inflammation, and inflammasome activity to IEC MHCII upregulation via an intestinal IL-18-IFNg axis. Understanding this process may be crucial for determining the contribution of IEC MHCII to intestinal homeostasis, host defense, and tolerance.”
3. Multiplex Screening Assay for Identifying Cytotoxic CD8+ T Cell Epitopes
Chek Meng Poh,et al.Front Immunol. 2020.PMCID: PMC7078160
“The cytotoxicity of epitope-specific CD8+ T cells is usually measured indirectly through IFNγ production. Existing assays that directly measure this activity are limited mainly to measurements of up to two specificities in a single reaction. Here, we develop a multiplex cytotoxicity assay that allows direct, simultaneous measurement of up to 23 different specificities of CD8+ T cells in a single reaction. This can greatly reduce the amount of starting clinical materials for a systematic screening of CD8+ T cell epitopes. In addition, this greatly enhanced capacity enables the incorporation of irrelevant epitopes for determining the non-specific killing activity of CD8+ T cells, thereby allowing to measure the actual epitope-specific cytotoxicity activities. This technique is shown to be useful to study both human and mouse CD8+ T cells. Besides, our results from human PBMCs and three independent infectious animal models (MERS, influenza and malaria) further reveal that IFNγ expression by epitope-specific CD8+ T cells does not always correlate with their cell-killing potential, highlighting the need for using cytotoxicity assays in specific contexts (e.g., evaluating vaccine candidates). Overall, our approach opens up new possibilities for comprehensive analyses of CD8+ T cell cytotoxicity in a practical manner.”

了解更多抗小鼠CD8b单克隆抗体(clone:YTS 156.7)参考文献,请查看:抗小鼠CD8b抗体(克隆号YTS 156.7)参考文献

Syd Labs抗小鼠CD8b重组抗体(克隆号YTS 156.7),大鼠IgG2b Kappa(货号:PA007382.r2b)推荐同型对照抗体:

重组大鼠IgG2b同型对照抗体,体内实验级(In Vivo Grade Recombinant Rat IgG2b Isotype Control Antibody)

Syd Labs提供以下体内实验级重组抗小鼠CD8a单克隆抗体:

体内实验级重组抗小鼠CD8a单克隆抗体(克隆号2.43),大鼠IgG2b Kappa
体内实验级重组抗小鼠CD8a单克隆抗体(克隆号YTS 169.4),大鼠IgG2b Kappa
体内实验级重组抗小鼠CD8a单克隆抗体(克隆号YTS 105.18),大鼠IgG2b Kappa
体内实验级重组抗小鼠CD8a单克隆抗体(克隆号53-6.72),大鼠IgG2a Kappa
体内实验级重组抗小鼠CD8 (Lyt 2.1) 单克隆抗体(克隆号116-13.1),小鼠IgG2a Kappa

背景知识

The rat anti-mouse CD8b monoclonal antibody YTS 156.7 (大鼠抗小鼠CD8b单克隆抗体)(rat IgG2b kappa) reacts with the mouse CD8b protein (T-cell surface glycoprotein CD8 beta chain, Lyt-3 or Ly-3) encoded by the mouse cd8b gene that encodes the CD8b chain of the dimeric CD8 protein. The mouse CD8 protein is primarily responsible for cell-mediated immune defense and T-cell development.

Our recombinant YTS 156.7 antibodies(重组抗小鼠CD8b单克隆抗体) have a part (variable regions) or complete amino acid sequences of the rat anti-mouse CD8b monoclonal antibody(大鼠抗小鼠CD8b抗体)(hybridoma clone name or number: YTS 156.7).

请记住我们的产品信息: 体内实验级重组抗小鼠CD8b单克隆抗体,大鼠IgG2b Kappa(克隆号YTS 156.7): PA007382.r2b Syd Labs In vivo Grade Recombinant Anti-mouse CD8b Monoclonal Antibody, Rat IgG2b Kappa (Clone: YTS 156.7)

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