BioXcell熱銷產(chǎn)品推薦--InVivoPlus anti-mouse PD-L1 (B7-H1)
產(chǎn)品描述:
BioXcell InVivoPlus anti-mouse PD-L1 10F.9G2單克隆抗體與小鼠PD-L1(也稱為B7-H1或CD274)反應(yīng)。PD-L1是屬于Ig超家族的B7家族的I型跨膜蛋白,分子量為40kDa。PD-L1在T淋巴細(xì)胞、B淋巴細(xì)胞、NK細(xì)胞、樹(shù)突狀細(xì)胞以及IFNγ刺激的單核細(xì)胞、上皮細(xì)胞和內(nèi)皮細(xì)胞上表達(dá)。PD-L1與CD4和CD8胸腺細(xì)胞以及活化的T和B淋巴細(xì)胞和骨髓細(xì)胞上的受體PD-1結(jié)合。PD-L1與PD-1的結(jié)合導(dǎo)致抑制TCR介導(dǎo)的T細(xì)胞增殖和細(xì)胞因子產(chǎn)生。PD-L1被認(rèn)為在腫瘤免疫逃逸中起著重要作用。誘導(dǎo)的PD-L1表達(dá)在許多腫瘤中很常見(jiàn),并導(dǎo)致腫瘤細(xì)胞對(duì)CD8 T細(xì)胞介導(dǎo)的裂解的抗性增加。在黑色素瘤的小鼠模型中,可以通過(guò)用阻斷PD-L1和PD-1之間相互作用的抗體進(jìn)行治療,暫時(shí)抑制腫瘤生長(zhǎng)。10F.9G2抗體已被證明可以阻斷PD-L1和PD-1之間以及PD-L1和B7-1之間的相互作用(CD80)。
產(chǎn)品詳情:
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產(chǎn)品名稱 |
InVivoPlus anti-mouse PD-L1 (B7-H1) |
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產(chǎn)品貨號(hào) |
BP0101 |
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產(chǎn)品規(guī)格 |
5/25/50/100mg |
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反應(yīng)種屬 |
Mouse |
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克隆號(hào) |
10F.9G2 |
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同種型 |
Rat IgG2b, κ |
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免疫原 |
Mouse CD274 |
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實(shí)驗(yàn)應(yīng)用 |
in vivo PD-L1 blockade |
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產(chǎn)品形式 |
PBS, pH 6.5,Contains no stabilizers or preservatives |
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純度 |
>95%, Determined by SDS-PAGE |
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聚合 |
<5%, Determined by SEC |
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無(wú)菌處理 |
0.2 μm filtration |
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純化方式 |
Protein G |
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RRID |
AB_10949073 |
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分子量 |
150 kDa |
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小鼠病原檢測(cè) |
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 |
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保存條件 |
抗體原液保存在4°C,不能冷凍保存。 |
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推薦同型對(duì)照 |
InVivoPlus rat IgG2b isotype control, anti-keyhole limpet hemocyanin(貨號(hào)BP0090) |
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推薦抗體稀釋液 |
InVivoPure pH 6.5 Dilution Buffer(貨號(hào)IP0065) |
為什么選擇InVivoPlus抗體?
InVivoPlus級(jí)別的產(chǎn)品內(nèi)毒素含量更低,經(jīng)過(guò)多種實(shí)驗(yàn)驗(yàn)證,更適合用于體內(nèi)實(shí)驗(yàn)研究

該產(chǎn)品自上市已被多篇SCI文獻(xiàn)引用,品質(zhì)有保證,以下是部分已發(fā)表的文獻(xiàn)引用:
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應(yīng)用 |
文章 |
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體內(nèi)PD-L1阻斷 (in vivo PD-L1 blockade) |
1. Grasselly, C., et al. (2018). 'The Antitumor Activity of Combinations of Cytotoxic Chemotherapy and Immune Checkpoint Inhibitors Is Model-Dependent' Front Immunol 9: 2100. 2. Stathopoulou, C., et al. (2018). 'PD-1 Inhibitory Receptor Downregulates Asparaginyl Endopeptidase and Maintains Foxp3 Transcription Factor Stability in Induced Regulatory T Cells' Immunity 49(2): 247-263 e247. 3. Kim, J., et al. (2015). 'Memory programming in CD8(+) T-cell differentiation is intrinsic and is not determined by CD4 help' Nat Commun 6: 7994. |
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體內(nèi)PD-L1阻斷,流式細(xì)胞術(shù) (in vivo PD-L1 blockade, Flow Cytometry) |
1. Aloulou, M., et al. (2016). 'Follicular regulatory T cells can be specific for the immunizing antigen and derive from naive T cells' Nat Commun 7: 10579. 2. Ngiow, S. F., et al. (2015). 'A Threshold Level of Intratumor CD8+ T-cell PD1 Expression Dictates Therapeutic Response to Anti-PD1' Cancer Res 75(18): 3800-3811. 3. Rutigliano, J. A., et al. (2014). 'Highly pathological influenza A virus infection is associated with augmented expression of PD-1 by functionally compromised virus-specific CD8+ T cells' J Virol 88(3): 1636-1651. |
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