重组抗人HLA class II DR/DQ单抗(9.3F10) | Syd Labs PA007478

重组抗人HLA class II DR/DQ单抗(9.3F10) Syd Labs PA007478 - 武汉多找找科技

重组抗人HLA class II DR/DQ单抗(9.3F10) | Syd Labs PA007478

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体内实验级重组抗人HLA class II DR/DQ单克隆抗体,小鼠IgG2a Kappa(克隆号:9.3F10,Syd Labs货号:PA007478),适用于体外和体内研究,纯度>95%。其不变区为小鼠Mouse IgG2a Kappa (mIgG2a或m2a),可与重组小鼠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。

产品参数

货号 PA007478
产品名称重组抗人HLA class II DR/DQ单抗(9.3F10) | Syd Labs PA007478
英文名 In vivo Grade Recombinant Anti-Human HLA class II DR/DQ Monoclonal Antibody, Mouse IgG2a Kappa (Clone: 9.3F10)
供货商名称 Syd Labs, Inc.
品牌名 Syd Labs
别称 beta1 domain MHC class II HLA DPB, CELIAC1, class II HLA beta chain, MHC class II HLA-DR, DP, DQ
概述 Syd Labs提供重组小鼠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 9.3F10
同种型 小鼠 IgG2a 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,以及用于研究受人HLA class II DR/DQ蛋白影响的生物途径的测定。
免疫源 抗人HLA class II DR/DQ单克隆抗体(克隆:9.3F10)在哺乳动物细胞中产生
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 体内实验级重组抗人HLA class II DR/DQ单克隆抗体 ,小鼠IgG2a Kappa(克隆号9.3F10)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 PA007478 Syd Labs提供重组小鼠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。
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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,以及用于研究受人HLA class II DR/DQ蛋白影响的生物途径的测定。

文献

抗人HLA class II DR/DQ单克隆抗体,体内实验级重组,小鼠IgG2a Kappa(克隆号9.3F10)(In vivo Grade Recombinant Anti-Human HLA class II DR/DQ Monoclonal Antibody, Mouse IgG2a Kappa (Clone: 9.3F10),货号:PA007478 Syd Labs)

人类主要组织相容性复合体 II 类分子(MHC-II,即 HLA II 类分子)在提呈外源性抗原并激活 CD4+ T 细胞介导的体液与细胞免疫应答中占据核心地位。其中,HLA-DR、HLA-DP 和 HLA-DQ 是三种主要的抗原递呈异二聚体蛋白。对于免疫学研究而言,具备广谱识别特性的抗人HLA-DR/DP/DQ单抗(如广为人知的 F3.3抗体 克隆及结合特定表型的 9.3F10 克隆)是解析免疫激活机制的重磅工具。这类抗体能够特异性结合转运与表达于专业抗原提呈细胞(APC)及活化 T 细胞表面的 HLA-II 类分子,在肿瘤免疫微环境检测、自身免疫性疾病发病机制研究以及器官移植排斥反应监测等领域中扮演着不可替代的角色。
为了保障基础研究与药物前沿探索的准确性,Syd Labs 与同类品牌(如 BioXCell 等)共同为全球科研机构提供高规格的体内实验级重组抗体。Syd Labs 提供的重组抗人HLA-DR/DP/DQ单抗(如 F3.3抗体 与 9.3F10 克隆等规格)采用严谨的哺乳动物细胞重组表达平台打造,具备极高的靶向特异性与批间稳定性。产品针对体内(in vivo)动物模型及敏感的体外细胞功能分析进行了深度优化,严格把控内毒素水平(Low Endotoxin),且不含任何影响细胞活性或带来非特异性干扰的载体蛋白与化学防腐剂,可有效配合小鼠 IgG2a 同型对照抗体使用,为移植免疫、肿瘤免疫疗法开发及免疫检查点相关实验提供高度严谨、可重复的数据保障。

抗人HLA class II DR/DQ单抗(9.3F10)部分引用文献:

1. Crossreactivity of a human autoimmune TCR is dominated by a single human leukocyte antigen residue
Newell, E., et al. J Clin Invest. 2014 Oct;124(10):4277-89. PMID: 25225671
“The study utilized anti-HLA-DR/DQ antibody (9.3F10) and anti-HLA-A2 (BB7.2) to assess the crossreactivity of the Ob.1A12 TCR in Jurkat cells stained with peptide/MHC tetramers and analyzed by flow cytometry. …The Ob.1A12 TCR recognized multiple self-peptides presented by HLA-DR, with a single HLA residue playing a dominant role in this crossreactivity. …In vivo experiments in HLA-DR-transgenic mice confirmed the autoimmune potential of the Ob.1A12 TCR, with TCR-transduced Jurkat cells co-cultured with antigen-presenting cells to measure activation.”

2. Self-reactive human CD4 T cell clones form unusual immunological synapses
Singh, R., et al. J Exp Med. 2012 Feb 13;209(2):335-52. PMID: 22291028
“The study used anti-HLA-DR/DQ antibody (9.3F10) and anti-HLA-DR (L243) to block MHC class II and investigate synapse formation in self-reactive CD4 T cell clones in a humanized mouse model. …Two-photon microscopy visualized synapse formation in lymph nodes, showing that 9.3F10 significantly reduced synapse stability and T cell activation. …T cell receptor signaling was assessed by measuring calcium flux upon antigen recognition.”

3. Interleukin 2-Antibody and Tumor Necrosis Factor-Antibody Fusion Proteins Induce Different Antitumor Immune Responses In Vivo
Christ, O., et al. Clin Cancer Res. 2001 May;7(5):1385-97. PMID: 11350943
“The study employed anti-HLA-DR/DQ antibody (clone 9.3F10), anti-CD80 (clone BB1), and anti-CD86 (clone IT2.2) for blocking experiments in SCID mice bearing human tumor xenografts. …IL-2 and TNF fusion proteins were administered intravenously, with tumor growth monitored over 21 days. …Flow cytometry confirmed HLA-DR/DQ expression on tumor cells, and the combination of IL-2 and TNF fusion proteins enhanced CD8+ T cell infiltration into tumors.”

4. CD4-Positive and CD8-Positive Cytotoxic T Lymphocytes Contribute to the Control of Cryptococcus neoformans in the Lungs of Mice
Kawakami, H., et al. Clin Diagn Lab Immunol. 1999 Mar;6(2):236-41. PMID: 10092809
“C57BL/6 mice were injected intraperitoneally with 0.5 mg of anti-HLA-DR/DQ mAb (9.3F10) 1 day before and 2 days after Cryptococcus neoformans infection. …The role of CD4+ and CD8+ T cells in controlling pulmonary infection was assessed, with flow cytometry quantifying T cell populations in lung tissues. …Depletion of CD4+ or CD8+ T cells increased fungal burden, demonstrating their contribution to host defense against Cryptococcus neoformans.”

5. Human Mycobacterium tuberculosis-reactive CD4+ T-cell clones from healthy, latently infected individuals
Demkowicz, A., et al. Infect Immun. 1991 Aug;59(8):2737-43. PMID: 1879230
“The study used 25 microg/mL of anti-HLA-DR/DQ antibody (9.3F10) or anti-HLA class I (W6/32) to preincubate B cells, confirming MHC class II-restricted antigen presentation. …CD4+ T cell clones from healthy individuals with latent Mycobacterium tuberculosis infection were isolated, and proliferation assays verified their specificity to mycobacterial antigens. …Flow cytometry confirmed MHC class II expression on antigen-presenting B cells, establishing that CD4+ T cell responses were restricted by HLA-DR/DQ molecules.”