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BioXCell熱銷產(chǎn)品--RecombiMAb anti-mouse CTLA-4 (CD152) (LALA-PG)
產(chǎn)品描述:
9D9-CP008單克隆抗體是原始9D9單克隆抗體的重組嵌合型抗體。可變結構域序列與原始9D9克隆號相同,但是恒定區(qū)序列已經(jīng)從小鼠IgG2b變?yōu)樾∈驣gG2a。9D9-CP008單克隆抗體在Fc片段中也含有LALA-PG突變,使其無法與內(nèi)源性Fcγ受體結合。
9D9-CP008單克隆抗體能與小鼠CTLA-4(細胞毒性T淋巴細胞抗原-4)反應,CTLA-4也稱為CD152。CTLA-4是一種33 kDa的細胞表面受體,由屬于免疫球蛋白超家族CD28家族的Ctla4基因編碼。CTLA-4在活化的T淋巴細胞和B淋巴細胞上表達。CTLA-4在結構上類似于T細胞共刺激蛋白CD28,兩種分子都與B7家族成員B7-1 (CD80)和B7-2 (CD86)結合。在與配體結合時,CTLA-4負調(diào)節(jié)細胞介導的免疫反應。CTLA-4在誘導和/或維持免疫耐受、胸腺細胞發(fā)育和保護性免疫調(diào)節(jié)中起作用。CTLA-4在免疫下調(diào)中的關鍵作用已經(jīng)在CTLA-4缺陷小鼠中得到證實,這些小鼠在3-5周齡時由于淋巴增生性疾病的發(fā)展而死亡。CTLA-4目前是腫瘤免疫治療中的熱門免疫檢查點靶點之一。
產(chǎn)品詳情:
產(chǎn)品名稱 | RecombiMAb anti-mouse CTLA-4 (CD152) (LALA-PG)/欣博盛生物 |
產(chǎn)品貨號 | CP008 |
產(chǎn)品規(guī)格 | 1mg |
反應種屬 | Mouse |
克隆號 | 9D9-CP008 |
同種型 | Mouse IgG2b(switched from mouse IgG2a) |
免疫原 | Not available or unknown |
實驗應用 | in vivo CTLA-4 neutralization* Western blot* *Reported for the original mouse IgG2b 9D9 antibody |
產(chǎn)品形式 | PBS, pH 7.0,Contains no stabilizers or preservatives |
純度 | >95%, Determined by SDS-PAGE |
聚合 | <5%, Determined by SEC |
無菌處理 | 0.2 µm filtration |
純化方式 | Protein A |
分子量 | 150 kDa |
小鼠病原檢測 | Ectromelia/Mousepox Virus: Negative Hantavirus: Negative K Virus: Negative Lactate Dehydrogenase-Elevating Virus: Negative Lymphocytic Choriomeningitis virus: Negative Mouse Adenovirus: Negative Mouse Cytomegalovirus: Negative Mouse Hepatitis Virus: Negative Mouse Minute Virus: Negative Mouse Norovirus: Negative Mouse Parvovirus: Negative Mouse Rotavirus: Negative Mycoplasma Pulmonis: Negative Pneumonia Virus of Mice: Negative Polyoma Virus: Negative Reovirus Screen: Negative Sendai Virus: Negative Theiler’s Murine Encephalomyelitis: Negative |
保存條件 | 抗體原液保存在4°C,不能冷凍保存。 |
推薦抗體稀釋液 | InVivoPure pH 7.0 Dilution Buffer(貨號IP0070) |
該產(chǎn)品自上市已被多篇SCI文獻引用,品質(zhì)有保證,以下是部分已發(fā)表的文獻引用:
應用 | 文章 |
體內(nèi)CTLA-4中和 (in vivo CTLA-4 neutralization) | 1. Dai, M., et al. (2015). 'Curing mice with large tumors by locally delivering combinations of immunomodulatory antibodies' Clin Cancer Res 21(5): 1127-1138. 2. Zippelius, A., et al. (2015). 'Induced PD-L1 expression mediates acquired resistance to agonistic anti-CD40 treatment' Cancer Immunol Res 3(3): 236-244. 3. Redmond, W. L., et al. (2014). 'Combined targeting of costimulatory (OX40) and coinhibitory (CTLA-4) pathways elicits potent effector T cells capable of driving robust antitumor immunity' Cancer Immunol Res 2(2): 142-153. 4. Condamine, T., et al. (2014). 'ER stress regulates myeloid-derived suppressor cell fate through TRAIL-R-mediated apoptosis' J Clin Invest 124(6): 2626-2639. 5. Muller, P., et al. (2014). 'Microtubule-depolymerizing agents used in antibody-drug conjugates induce antitumor immunity by stimulation of dendritic cells' Cancer Immunol Res 2(8): 741-755. 6. Bulliard, Y., et al. (2013). 'Activating Fc gamma receptors contribute to the antitumor activities of immunoregulatory receptor-targeting antibodies' J Exp Med 210(9): 1685-1693. |
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