BioXCell--RecombiMAb anti-mouse CTLA-4 (CD152) (LALA-PG)

9D9-CP008单克隆抗体是原始9D9单克隆抗体的重组嵌合型抗体。可变结构域序列与原始9D9克隆号相同，但是恒定区序列已经从小鼠IgG2b变为小鼠IgG2a。9D9-CP008单克隆抗体在Fc片段中也含有LALA-PG突变，使其无法与内源性Fcγ受体结合。

9D9-CP008单克隆抗体能与小鼠CTLA-4(细胞毒性T淋巴细胞抗原-4)反应，CTLA-4也称为CD152。CTLA-4是一种33 kDa的细胞表面受体，由属于免疫球蛋白超家族CD28家族的Ctla4基因编码。CTLA-4在活化的T淋巴细胞和B淋巴细胞上表达。CTLA-4在结构上类似于T细胞共刺激蛋白CD28，两种分子都与B7家族成员B7-1 (CD80)和B7-2 (CD86)结合。在与配体结合时，CTLA-4负调节细胞介导的免疫反应。CTLA-4在诱导和/或维持免疫耐受、胸腺细胞发育和保护性免疫调节中起作用。CTLA-4在免疫下调中的关键作用已经在CTLA-4缺陷小鼠中得到证实，这些小鼠在3-5周龄时由于淋巴增生性疾病的发展而死亡。CTLA-4目前是肿瘤免疫治疗中的热门免疫检查点靶点之一。

产品详情：

产品名称	RecombiMAb anti-mouse CTLA-4 (CD152) (LALA-PG)/欣博盛生物
产品货号	CP008
产品规格	1mg
反应种属	Mouse
克隆号	9D9-CP008
同种型	Mouse IgG2b(switched from mouse IgG2a)
免疫原	Not available or unknown
实验应用	in vivo CTLA-4 neutralization* Western blot* *Reported for the original mouse IgG2b 9D9 antibody
产品形式	PBS, pH 7.0,Contains no stabilizers or preservatives
纯度	>95%, Determined by SDS-PAGE
聚合	<5%, Determined by SEC
无菌处理	0.2 µm filtration
纯化方式	Protein A
分子量	150 kDa
小鼠病原检测	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
保存条件	抗体原液保存在4°C，不能冷冻保存。
推荐抗体稀释液	InVivoPure pH 7.0 Dilution Buffer（货号IP0070）/欣博盛生物

该产品自上市已被多篇SCI文献引用，品质有保证，以下是部分已发表的文献引用：

应用

文章

体内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.