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          1. 華拓生物可供應幾萬種生物試劑
            專業提供抗體抗原、多肽、蛋白、細胞等試劑以及相關定制服務
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            IVD診斷抗體抗原系列
            程序性死亡配體1抗體/PD-L1 Antibody
            產品名稱 : 程序性死亡配體1抗體/PD-L1 Antibody
            產品類別 : IVD診斷抗體原料
            品  牌 : GenomeMe
            貨  號 : IHC411
            規  格 : 0.1ml/1ml
            詳細信息
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            產品說明
            背景描述Description:
            程序性死亡配體1(PD-L1)又稱CD274或B7同源物1(B7-H1),是一種跨膜蛋白,通過與程序性死亡-1(PD-1)受體的結合,抑制免疫系統,使腫瘤細胞抵抗CD8+T細胞介導的殺傷。PD-L1的過度表達可能使癌細胞逃避宿主免疫系統的作用。在腎細胞癌中,PD-L1的表達上調與腫瘤侵襲性和死亡風險增加有關,而在卵巢癌中,PD-L1的高表達會導致明顯的不良預后。PD-L1還與系統性紅斑狼瘡和皮膚黑色素瘤有關。當與CD8+腫瘤浸潤淋巴細胞密度聯合考慮時,PD-L1的表達水平可能是預測多種癌癥類型的有用指標,包括III期非小細胞肺癌、激素受體陰性乳腺癌和前哨淋巴結黑色素瘤。
            Programmed Death-Ligand 1 (PD-L1), also known as CD274 or B7 Homolog 1 (B7-H1), is a transmembrane protein involved in suppressing the immune system and rendering tumor cells resistant to CD8+ T cell-mediated lysis through binding of the Programmed Death-1 (PD-1) receptor. Overexpression of PD-L1 may allow cancer cells to evade the actions of the host immune system. In renal cell carcinoma, upregulation of PD-L1 has been linked to increased tumor aggressiveness and risk of death, and, in ovarian cancer, higher expression of this protein has lead to significantly poorer prognosis. PD-L1 has also been linked to systemic lupus erythematosus and cutaneous melanoma. When considered in adjunct with CD8+ tumor-infiltrating lymphocyte density, expression levels of PD-L1 may be a useful predictor of multiple cancer types, including stage III non-small cell lung cancer, hormone receptor negative breast cancer, and sentinel lymph node melanoma.
             
            Specifications:
            Clone IHC411
            Source Rabbit Monoclonal
            Positive Control Tonsil, Lung Adenocarcinoma
            Dilution Range 1:50-1:200
             
            參考文獻References:
            Ostrand-Rosenberg S, et al. J Immunol. 2014; 193:3835-41.
            Tokito T, et al. Eur J Cancer. 2016; 55:7-14.
            Park IH, et al. Clin Breast Cancer. 2016; 16:51-8.
            Kakavand H, et al. Mod Pathol. 2015; 28: 1535-44.
            Xia B, et al. Immunotherapy. 2016; 8:279-98.
            Patel SP, et al. Mol Cancer Ther. 2015; 14:847-56.
            Singh BP, et al. Cancers (Basel). 2016; 8.
            Chemnitz JM, et al. J Immunol. 2004; 173:945–54.
            Thompson RH, et al. Proc Natl Acad Sci USA. 2004; 101:17174–9.
            Hamanishi J, et al. Proc Natl Acad Sci USA. 2007; 104:3360–5.
            Mozaffarian N, et al. Rheumatology, 2008; 47:1335–41.
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