重组抗小鼠GITR单抗(DTA-1)流式 | Syd Labs PA007502.r2b

重组抗小鼠GITR单抗流式(DTA-1) Syd Labs PA007502.r2b - 武汉多找找科技

重组抗小鼠GITR单抗(DTA-1)流式 | Syd Labs PA007502.r2b

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Syd Labs重组抗小鼠GITR单克隆抗体(克隆号DTA-1) ,大鼠IgG2b Lambda(货号:PA007502.r2b)是用哺乳动物细胞生产的重组抗体,其可变区序列是从大鼠抗小鼠GITR单克隆抗体(克隆号:DTA-1)中提取的,可用于流式细胞术和免疫组织化学-冷冻等研究,纯度>95%。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: PA007502.r2b 分类: ,

产品参数

货号 PA007502.r2b
产品名称重组抗小鼠GITR单抗(DTA-1)流式 | Syd Labs PA007502.r2b
英文名 Recombinant Anti-mouse GITR Monoclonal Antibody (Clone: DTA-1), Rat IgG2b Lambda
供货商名称 Syd Labs, Inc.
品牌名 Syd Labs
别称 糖皮质激素诱导的 TNFR 相关蛋白 TNFRSF18; 肿瘤坏死因子受体超家族成员 18
概述 重组抗小鼠GITR单克隆抗体是用哺乳动物细胞生产的,其可变区序列是从大鼠抗小鼠GITR单克隆抗体(克隆号:DTA-1)中提取的,适合体外和体内研究。
克隆号 DTA-1
同种型 大鼠 IgG2b, lambda
特异性 该重组 DTA-1抗体与小鼠 GITR 蛋白特异性结合
免疫源 重组抗小鼠GITR单克隆抗体 (克隆:DTA-1)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GITR单克隆抗体(克隆号DTA-1) ,大鼠IgG2b Lambda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 PA007502.r2b Syd Labs重组抗小鼠GITR单克隆抗体是用哺乳动物细胞生产的,其可变区序列是从大鼠抗小鼠GITR单克隆抗体(克隆号:DTA-1)中提取的,适合体外和体内研究。
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GITR单克隆抗体(克隆号DTA-1) ,大鼠IgG2b Lambda(Recombinant Anti-mouse GITR Monoclonal Antibody (Clone: DTA-1), Rat IgG2b Lambda,货号:PA007502.r2b Syd Labs)

大鼠抗小鼠GITR单克隆抗体DTA-1(大鼠IgG2b lambda)可与小鼠GITR蛋白(糖皮质激素诱导的TNFR相关蛋白或肿瘤坏死因子受体超家族18,TNFRSF 18)发生反应。DTA-1单克隆抗体可与主要由CD4+CD25+调节性T细胞(Treg)以及CD25+ CD4+ CD8-胸腺细胞表达的小鼠GITR反应。

我们的重组DTA-1抗体包含大鼠抗小鼠GITR单克隆抗体(杂交瘤克隆名称或编号:DTA-1)的部分(可变区)或完整氨基酸序列。

抗小鼠GITR单抗(DTA-1)流式部分参考文献:

1. A Comparison of Murine PD-1 and PD-L1 Monoclonal Antibodies
Bu, M. T., et al. Monoclon Antib Immunodiagn Immunother. 2022 Aug;41(4):202-209. PMID: 35925787
“Unconjugated and fluorophore-conjugated PD-1 mAbs (1A12, rat IgG2a; RMP1-14, rat IgG2a; and RMP1-30, rat IgG2b) and PD-L1 mAbs (10F.9G2, rat IgG2b; MIH6, rat IgG2a) were purchased from…Owing to the widespread use of both PD-1 mAbs 1A12 and RMP1-14 in experimental mouse models, we compared the avidities of these two mAbs. …The 1A12 antimouse PD-1 mAb bound to mPD-1–transfected Jurkat cells in a dose-dependent manner with an apparent affinity of 0.42 nM, while RMP1-14 antibody bound with a much weaker apparent affinity of 28.8 nM. …This result was also seen with 1A12 and RMP1-14 mAbs from a different vendor (Fig. S1). …In case the lower avidity of RMP-1-14 (anti-mouse CD279 antibody) was a consequence of transfection, we assayed the antibody binding to exhausted murine CD8 T cells naturally expressing PD-1…”

2. Dying cells expose a nuclear antigen cross-reacting with anti-PD-1 monoclonal antibodies
Metzger, P., et al. Sci Rep. 2018 Jun 11;8(1):8810. PMID: 29892077
“We assessed PD-1 expression by flow cytometry and compared the two mainly used antibody clones (29 F.1A12 and RMP1-14 antibodies), which were also included in the above-mentioned study. …We observed PD-1 staining exclusively in the dead cell fraction for both clones 29 F.1A12 and RMP1-14 mAb, respectively…”

3. The Antitumor Activity of Combinations of Cytotoxic Chemotherapy and Immune Checkpoint Inhibitors Is Model-Dependent
Grasselly, C., et al. Front Immunol. 2018 Oct 9;9:2100. PMID: 30356816
“Anti-PD1 antibody(clone RMP1-14) or anti-PDL1 (clone 10F.9G2) mAb (12,5 mg/kg, ip, q1wk) were administered in combination with (A,C) methotrexate (1 mg/kg, ip, q1wk), vinblastine (0.1 mg/kg, ip, q1wk), doxorubicin(1 mg/kg, ip, q1wk) and cisplatin(1 mg/kg,ip, q1wk, MVAC) in SC bladder cancer MB49 and MBT-2, and with (B) cyclophosphamide (CTX, 100 mg/kg, ip, q1wk) and doxorubicin (DOX, 2 mg/kg, ip, q1wk) in SC metastatic breast cancer 4T1, and with (D) capecitabine (CAPE, 250 mg/kg, po 5 days a week) and oxaliplatin (OXA, 5 mg/kg, ip, q1wk) in SC colorectal cancer MC38. …Effect of anti-PD1 antibody (clone RMP1-14) or anti-PDL1 (clone 10F.9G2) antibody, 12,5 mg/kg, i.p., q1wk, in combination with cyclophosphamide (CTX) 100 mg/kg, i.p, q1wk and doxorubicin (DOX) 2 mg/kg, i.p, q1wk in SC metastatic breast cancer 4T1 (A), methotrexate 1mg/kg, i.p, q1wk and vinblastine 0,1 mg/kg, i.p, q1wk and doxorubicin 1 mg/kg, i.p, q1wk and cisplatin 1 mg/kg i.p, q1wk (MVAC) in SC bladder cancer MB49 (B), Data are shown as Mean + SEM, n = 5 to 6 (A), n = 6 (B).”

4. Type I MET inhibitors cooperate with PD-1 blockade to promote rejection of hepatocellular carcinoma
DeAzevedo, R., et al. J Immunother Cancer. 2024 Oct 30;12(10):e009690. PMID: 39477243
“On days 7, 11, 15, and 19, mice received 250 ug anti-PD-1 antibody RMP1-14 i.p. or isotype control antibody. …On days 7, 11, 15, and 19, mice received 250 ug anti-PD-1 mAb RMP1-14 i.p. or isotype control antibody. …In this system, mice were treated when measurable tumors emerged with 10 doses of c-Met inhibitor and 5 doses of the PD-1 antibody RMP1-14. …On days 2, 4, 6, 8, and 10 post-palpation, mice received 250 ug anti-PD-1 RMP1-14 antibody i.p. or isotype control antibody. …On days 2, 4, 6, 8, and 10 post-palpation, mice received 250 ug anti-PD-1 RMP1-14 mAb i.p. or isotype control antibody.”

5. Impact of mouse model tumor implantation site on acquired resistance to anti-PD-1 immune checkpoint therapy
Denis, M., et al. Front Immunol. 2023 Jan 10;13:1011943. PMID: 36703964
“When the tumor volume reached 150 mm3, mice were randomized and received first treatment of anti-PD-1 antibody (RMP1-14, 12.5 mg/kg per week, intraperitoneal (IP)). …The mice are randomized based on their weight and receive 48 hours after the operation their first anti-PD-1 treatments (RMP1-14, 12.5 mg/kg per week, IP)…”