重组29F.1A12抗体(CD279抗体、抗小鼠PD1单抗)流式 | Syd Labs PA007505.r2a

重组抗小鼠PD-1单抗流式(29F.1A12.1) Syd Labs PA007505.r2a - 武汉多找找科技

重组29F.1A12抗体(CD279抗体、抗小鼠PD1单抗)流式 | Syd Labs PA007505.r2a

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Syd Labs重组抗小鼠PD-1单克隆抗体(克隆号29F.1A12.1) ,大鼠IgG2a Kappa(货号:PA007505.r2a)是用哺乳动物细胞生产的重组抗体,可用于流式细胞术和免疫组织化学-冷冻等研究,纯度>95%。其不变区为大鼠Rat 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。

SKU: PA007505.r2a 分类: ,

产品参数

货号 PA007505.r2a
产品名称重组29F.1A12抗体(CD279抗体、抗小鼠PD1单抗)流式 | Syd Labs PA007505.r2a
英文名 Recombinant Anti-mouse PD-1 Monoclonal Antibody (Clone: 29F.1A12.1), Rat IgG2a Kappa
供货商名称 Syd Labs, Inc.
品牌名 Syd Labs
别称 抗小鼠PD 1抗体,抗小鼠pd-1单抗,小鼠PD-1单抗,小鼠CD279抗体,29F.1A12抗体,细胞程序性死亡蛋白 1
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 29F.1A12.1
同种型 大鼠 IgG2a Kappa
特异性 该重组 29F.1A12 抗体与小鼠 PD1 蛋白特异性结合
免疫源 重组抗小鼠PD1单克隆抗体 (克隆:29F.1A12)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,含0.09%叠氮化钠
偶联 非偶联
纯度 >95%(在还原条件下通过SDS-PAGE测定)
运输 重组抗小鼠PD-1单克隆抗体(克隆号29F.1A12.1) ,大鼠IgG2a 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 12个月,保存在2 至 8°C。 请勿冻结。
注意事项 PA007505.r2a 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。
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 流式细胞术(FC)和免疫组织化学-冷冻(IHC-F)。

文献

重组抗小鼠PD-1单克隆抗体(克隆号29F.1A12.1) ,大鼠IgG2a Kappa(Recombinant Anti-mouse PD-1 Monoclonal Antibody (Clone: 29F.1A12.1), Rat IgG2a Kappa,货号:PA007505.r2a Syd Labs)

大鼠抗小鼠PD-1单克隆抗体29F.1A12(大鼠IgG2a kappa)可与由小鼠Pdcd1基因编码的小鼠PD-1蛋白(程序性死亡-1或CD279)发生反应,该蛋白是免疫球蛋白超家族CD28家族的成员。PD-1有两个配体即PD-L1和PD-L2,二者均属于B7家族。研究表明,在黑色素瘤小鼠模型中,通过抗小鼠PD-1和抗小鼠PD-L1抗体进行治疗可以阻断PD-L1蛋白与其受体PD-1蛋白之间的相互作用,从而使肿瘤生长得到暂时性抑制。29F.1A12单克隆抗体能够阻断小鼠PD-L1蛋白和小鼠PD-L2蛋白与小鼠PD-1蛋白的结合。我们的重组29F.1A12抗体包含大鼠抗小鼠PD-1单克隆抗体(杂交瘤克隆名称或编号:29F.1A12)的部分(可变区)或完整的氨基酸序列。

29F.1A12抗体(CD279抗体、抗小鼠PD1单抗)流式部分参考文献:

1. Anti-PD-1 therapy triggers Tfh cell–dependent IL-4 release to boost CD8 T cell responses in tumor-draining lymph nodes.
Ruggiu, M., et al. J Exp Med. 2024;221(4):e20232104. PMID: 38417020
“Lymph node cells were stained ex vivo with a different anti-PD-1 mAb clone that did not interfere with the injected mAb (Polesso et al., 2021) to link in vivo labeling with PD-1 surface expression levels. …(B) Representative FACS dot plot showing in vivo labeling by AF594-labeled anti-PD-1 mAb (clone RMP1-14) and ex vivo staining by anti-PD-1 antibody (clone 29F.1A12). …anti-mouse PD1-BX036 (purified clone 29F.1A12 from…”

2. Distinct antibody clones detect PD-1 checkpoint expression and block PD-L1 interactions on live murine melanoma cells.
Martins, C., et al. Sci Rep. 2022;12(1):12491. PMID: 35864188
“Similarly, in preclinical cancer models, several PD-1 blocking ab clones, including 29F.1A12 (anti-mouse PD-1 antibody), thwart tumor progression 4 , 5 , 6 , 7 , 8. …For example, TME-infiltrating macrophages and natural killer (NK) cells both express PD-1, the blockade of which by 29F.1A12 (anti-mouse PD-1 mAb) contributes to tumor growth suppression and prolonged survival 10 , 11. …29F.1A12 antibody recognizes PD-1 on B16-F10 and other murine tumor lines, suppresses cancer cell-intrinsic PD-1 receptor signaling, and inhibits resultant tumor growth in three-dimensional (3D) culture and tumor-bearing mice 5 , 7…”

3. Dying cells expose a nuclear antigen cross-reacting with anti-PD-1 monoclonal antibodies.
Metzger, P., et al. Sci Rep. 2018;8(1):9040. PMID: 29892077
“In addition, PD-1 staining (clone 29F1A12) uncovered a FSC-H low population predominantly positive for PD-1. …PD-1 (clone 29F.1A12) and fixable viability dye (FVD) staining was assessed by flow cytometry. …PD-1 staining (clone 29F.1A12) in these cells could be due to binding of an intracellular PD-1 pool that becomes accessible in cells with leaky membranes…Again, PD-1 mAb staining (clone 29F.1A12) was found in both PD-1 wild-type and knock-out cells in the dead cell fraction, indicative of unspecific binding. …We assessed PD-1 expression by flow cytometry and compared the two mainly used antibody clones (29F.1A12 and RMP1-14), which were also included in the above-mentioned study.”

4. Adaptive resistance to therapeutic PD-1 blockade is associated with upregulation of alternative immune checkpoints.
Koyama, S., et al. Nat Commun. 2016;7:10501. PMID: 26883990
“Fluorescent conjugated anti-PD-1 antibody is the same clone (29F.1A12) as the therapeutic antibody. …PD-1-blocking antibody (clone 29F.1A12), TIM-3-blocking antibody (clone RMT3-23) and their isotype controls (clone 2A3) were injected intraperitoneally into the mice for therapeutic treatment (three times a week, 200 µg for PD1 and 100 µg for TIM-3 per dose).”

5. The PD-1 Pathway Regulates Development and Function of Memory CD8+ T Cells following Respiratory Viral Infection.
Pauken, K. E., et al. Cell Rep. 2020;31(13):107827. PMID: 32610128
“WT B6 mice were treated with anti-PD-1 antibody (clone 29F.1A12) or isotype control antibody (rat IgG2a) on days -1, 2, and 5 and harvested on day 8 p.i., or treated on days -1, 2, 5, and 8 and harvested on day 60+ p.i. PD-L1/L2 DKO mice were included as a control. …For in vivo antibody blockade experiments, WT C57BL/6 mice were given 200 µg per mouse per injection of rat anti-PD-1 antibody (clone 29F.1A12) or isotype control antibody (Rat IgG2a, clone 2A3) on days -1, 2, and 5 p.i. and analyzed at day 8 p.i., or on days -1, 2, 5, and 8 p.i. and analyzed at day 60+ p.i…”