重组抗小鼠CD16 / CD32单克隆抗体(克隆号2.4G2) ,大鼠IgG2b Kappa | Syd Labs PA007389.r2b

重组抗小鼠CD16 / CD32单克隆抗体(克隆号2.4G2) ,体内实验级,大鼠IgG2b Kappa | Syd Labs PA007389.r2b

重组抗小鼠CD16 / CD32单克隆抗体(克隆号2.4G2) ,大鼠IgG2b Kappa | Syd Labs PA007389.r2b

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体内实验级重组抗小鼠CD16 / CD32单克隆抗体,大鼠IgG2b Kappa(克隆号:2.4G2,货号:PA007389.r2b)是用哺乳动物细胞生产的重组抗体,纯度>95%,适用于体内和体外研究,比如体内 Fc 受体阻断、流式细胞术Fc受体阻断等。Syd Labs PA007389.r2b不变区为大鼠Rat 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。

产品参数

货号 PA007389.r2b
产品名称重组抗小鼠CD16 / CD32单克隆抗体(克隆号2.4G2) ,大鼠IgG2b Kappa | Syd Labs PA007389.r2b
英文名 In Vivo Grade Recombinant Anti-mouse CD16/CD32 Monoclonal Antibody, Rat IgG2b Kappa (Clone: 2.4G2)
供货商名称 Syd Labs, Inc.
品牌名 Syd Labs
别称 小鼠Fc受体阻断抗体,小鼠2.4G2 Fc区,小鼠 CD16/CD32 Fc 阻断
概述 小鼠 CD16/CD32 Fc 阻断抗体 (2.4 G2 Fc 阻断抗体) 是一种用于小鼠 FcR 阻断试剂的抗小鼠 Fc 受体抗体。Syd Labs提供不同的同种型用于某些应用。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 2.4G2
同种型 大鼠 IgG2b kappa
应用 ELISA、流式细胞术、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CD16和CD32蛋白影响的生物途径的测定。小鼠Fc受体阻断剂和小鼠Fc受体阻断抗体。
免疫源 抗小鼠CD16/CD32单克隆抗体(克隆:2.4G2)在哺乳动物细胞中产生
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CD16 / CD32单克隆抗体,大鼠IgG2b Kappa(克隆号2.4G2) 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 PA007389.r2b Syd Labs抗小鼠CD16/CD32(克隆2.4G2):用于流式细胞术、免疫组织化学(IHC)和免疫沉淀(IP)。它对FcγRII(CD32)和FcγRIII(CD16)具有高度特异性,并可减少背景染色;它可能不会阻断所有Fc受体。克隆X54-5/7.1是流式细胞术和功能检测中用于Fc阻断的最广泛的抗小鼠FcγRI(CD64)克隆。它可以阻止非特异性 Fc 受体与单核细胞、巨噬细胞和树突状细胞结合,提高抗体特异性。
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、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CD16和CD32蛋白影响的生物途径的测定。小鼠Fc受体阻断剂和小鼠Fc受体阻断抗体。

文献

PA007389.r2b: Syd Labs体内实验级重组抗小鼠CD16/CD32单克隆抗体(克隆号2.4G2),大鼠IgG2b Kappa(In vivo Grade Recombinant Anti-mouse CD16/CD32 Monoclonal Antibody, Rat IgG2b Kappa (Clone: 2.4G2))

抗小鼠CD16 / CD32单抗(2.4G2)部分参考文献:

1. Signaling through the inhibitory Fc receptor FcγRIIB induces CD8 T cell apoptosis to limit T cell immunity
Anna B. Morris,et al.Immunity. 2020.PMCID: PMC7326381
“Effector CD8+ T cells are important mediators of adaptive immunity, and receptor-ligand interactions that regulate their survival may have therapeutic potential. Here, we identified a subset of effector CD8+ T cells that expressed the inhibitory Fc receptor FcγRIIB following activation and multiple rounds of division. CD8+ T cell-intrinsic genetic deletion of Fcgr2b increased CD8+ effector T cell accumulation, resulting in accelerated graft rejection and decreased tumor volume in mouse models. IgG antibody was not required for FcγRIIB-mediated control of CD8+ T cell immunity, and instead, the immunosuppressive cytokine Fgl2 was a functional ligand for FcγRIIB on CD8+ T cells, in that Fgl2 induced caspase 3/7-mediated apoptosis in Fcgr2b+ but not Fcgr2b−/− CD8+ T cells. Moreover, Increased expression of FcγRIIB correlated with freedom from rejection following withdrawal from immunosuppression in a clinical trial of kidney transplant recipients. Together, these findings demonstrate a cell-intrinsic coinhibitory function of FcγRIIB in regulating CD8+ T cell immunity.”
标签:小鼠 Fc 阻断试剂;2.4 G2抗体体内 Fc 受体阻断
2. Accelerated clearance and degradation of cell free HIV by neutralizing antibodies occurs via FcγRIIb on liver sinusoidal endothelial cells by endocytosis
James M. Turman,et al.J Immunol. 2021.PMCID: PMC7946731
“Neutralizing antibodies suppress HIV infection by accelerating viral clearance from blood circulation, in addition to neutralization. The elimination mechanism is largely unknown. We determined that human liver sinusoidal endothelial cells (LSEC) express FcγRIIb as the lone Fc gamma receptor, and, using humanized FcγRIIb mouse, we found that antibody-opsonized HIV pseudoviruses (Ab-HIV) were cleared considerably faster from circulation than HIV by LSEC FcγRIIb. Compared to humanized FcγRIIb expressing mice, HIV clearance was significantly slower in FcγRIIb KO mice. Interestingly, pentamix of neutralizing antibodies cleared HIV faster compared to polyclonal HIVIG, though the HIV antibody-antigen ratio was higher in immune complexes made of HIVIG and HIV than pentamix and HIV. The effector mechanism of LSEC FcγRIIb was identified to be endocytosis. Once endocytosed, both Ab-HIV and HIV localized to lysosomes. This suggests that clearance of HIV, endocytosis and lysosomal trafficking within LSEC occur sequentially, and that the clearance rate may influence downstream events. Most importantly, we have identified LSEC FcγRIIb-mediated endocytosis to be the Fc effector mechanism to eliminate cell free HIV by antibodies, which could inform development of HIV vaccine and antibody therapy.”
标签:抗小鼠CD16 / CD32单抗2.4G2;2.4 G2 Fc 阻断抗体
3. Plasmacytoid Dendritic Cells Take Up Opsonized Antigen Leading to CD4+ and CD8+ T Cell Activation In Vivo
Pia Björck,et al.J Immunol. 2008.PMCID: PMC2884144
“Plasmacytoid dendritic cells (pDC) are the body’s main source of IFN-α, but, unlike classical myeloid DC (myDC), they lack phagocytic activity and are generally perceived as playing only a minor role in Ag processing and presentation. We show that murine pDC, as well as myDC, express Fcγ receptors (CD16/CD32) and can use these receptors to acquire Ag from immune complexes (IC), resulting in the induction of robust Ag-specific CD4+ and CD8+ T cell responses. IC-loaded pDC stimulate CD4 + T cells to proliferate and secrete a mixture of IL-4 and IFN-γ, and they induce CD8+ T cells to secrete IL-10 as well as IFN-γ. In contrast, IC-loaded myDC induce both CD4+ and CD8+ T cells to secrete mainly IFN-γ. These results indicate that pDC can shape an immune response by acquiring and processing opsonized Ag, leading to a predominantly Th2 response.”
标签:Fcγ受体;小鼠 CD16/CD32 Fc 阻断抗体

了解更多抗小鼠CD16 / CD32单克隆抗体(clone:2.4G2)参考文献,请查看:抗小鼠CD16 / CD32抗体(克隆号2.4G2)参考文献

Syd Labs抗小鼠CD16 / CD32单克隆抗体(克隆号2.4G2),大鼠IgG2b Kappa(货号:PA007389.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人CD16、CD32和CD64单克隆抗体:

Recombinant Anti-human CD16 monoclonal antibody (Clone: 3G8)
Recombinant Anti-human CD32 monoclonal antibody (Clone: IV.3)
Recombinant Anti-human CD64 monoclonal antibody (Clone: H22)

Syd Labs提供以下体内实验级重组抗小鼠CD16、CD32单克隆抗体:

Recombinant Anti-mouse CD16/CD32 monoclonal antibody (Clone: 2.4G2)

Syd Labs提供以下重组抗人CD16、CD32和CD64单克隆抗体(流式细胞术用):

Recombinant Anti-human CD16 monoclonal antibody (Clone: 3G8) for flow cytometry
Recombinant Anti-human CD32 monoclonal antibody (Clone: IV.3) for flow cytometry
Recombinant Anti-human CD64 monoclonal antibody (Clone: H22) for flow cytometry

Syd Labs提供以下重组抗小鼠CD16、CD32单克隆抗体(流式细胞术用):

Recombinant Anti-mouse CD16/CD32 monoclonal antibody (Clone: 2.4G2) for flow cytometry

关于PA007389.r2b Syd Labs抗小鼠CD16/CD32抗体您可能还会搜索:

PA007389.r2b Syd Labs抗小鼠CD16/CD32抗体
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PA007389.m2aLA Syd Labs
PA007389.mf 小鼠Fc受体阻断抗体
PA007389.h1 小鼠 CD16/CD32 Fc阻断
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be0307 bioxcell

背景知识

重组2.4G2抗体(2.4G2抗体、抗小鼠CD16 / CD32单抗2.4G2)与小鼠CD16(FcγIII)和CD32(FcγII)受体蛋白结合。一些商业Fc封闭试剂的主要成分即为2.4G2抗体。大鼠、小鼠和人IgG Fc可与小鼠CD64(FcγI)结合。因此,重组2.4G2抗体可用于在流式细胞术、免疫组化、免疫沉淀和封闭实验中阻断IgG与小鼠Fc受体的非特异性结合。客户可根据自身应用选择不同的IgG同型。

最常用的小鼠Fc封闭试剂包括:

抗小鼠CD16/CD32(克隆2.4G2):用于流式细胞术、免疫组化(IHC)和免疫沉淀(IP)。它对FcγRII(CD32)和FcγRIII(CD16)具有高度特异性,可降低背景染色;但可能无法封闭所有Fc受体。克隆X54-5/7.1是流式细胞术和功能实验中最广泛使用的抗小鼠FcγRI(CD64)克隆,可防止单核细胞、巨噬细胞和树突状细胞上的非特异性Fc受体结合,提高抗体特异性。

正常小鼠血清、从小鼠血清中纯化的小鼠IgG或小鼠同型对照混合物:用于IHC和免疫荧光(IF)中的一般Fc封闭。价格便宜、使用方便,但特异性较低,甚至可能引入不需要的免疫球蛋白。我们的重组小鼠IgG抗体混合物价格实惠;各种IgG的比例经过优化且可调整,不含任何不需要的免疫球蛋白。

纯化的大鼠IgG或同型对照:用于流式细胞术。可作为封闭Fc受体的对照,但对Fc受体无特异性。悉得(Syd Labs)提供多种大鼠IgG同型对照。

牛血清白蛋白(BSA)或胎牛血清(FBS):用于Western Blot(WB)和IHC中的一般封闭。易于获得,可减少非特异性结合,但对Fc受体封闭效果较差。

商业Fc封闭溶液:用于流式细胞术、IHC和功能实验。通常经过预优化,效果显著,但比自制溶液更昂贵。

根据应用推荐的最佳小鼠Fc封闭试剂选择:

流式细胞术:抗小鼠CD16/CD32(克隆2.4G2)。

免疫组化(IHC)和免疫荧光(IF):正常小鼠血清、纯化的小鼠或大鼠IgG或同型对照,或商业Fc封闭试剂盒。我们的重组小鼠IgG抗体混合物和重组大鼠IgG同型对照价格实惠;各种IgG的比例经过优化且可调整,不含任何不需要的免疫球蛋白。

Western Blot和ELISA:BSA或FBS。

功能实验(例如封闭Fc介导的效应):商业Fc封闭试剂。

请记住我们的产品信息: 体内实验级重组抗小鼠CD16 / CD32单克隆抗体(克隆号2.4G2),大鼠IgG2b Kappa: PA007389.r2b Syd Labs In Vivo Grade Recombinant Anti-mouse CD16/CD32 Monoclonal Antibody, Rat IgG2b Kappa (Clone: 2.4G2)。