用户验证的应用
经验证应用
| 项目 | 详情 |
|---|---|
| Positive WB detected in | human placenta tissue, A375 cells, IFN gamma treated A549 cells, HepG2 cells, K-562 cells, mouse heart tissue, mouse skeletal muscle tissue, rat kidney tissue |
| Positive IP detected in | mouse heart tissue |
| Positive IHC detected in | human tonsillitis tissue, human stomach cancer tissue, mouse heart tissue Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0 |
| Positive IF-P detected in | human tonsillitis tissue |
推荐稀释说明
It is recommended that this reagent should be titrated in each testing system to obtain optimal results. Sample-dependent, Check data in validation data gallery.
详细信息
背景信息
PD-L1, also known as CD274 or B7H1, stands for programmed cell death ligand 1. It is a type I transmembrane protein that is thought to repress immune responses by binding to its receptor (PD1), thus inhibiting T-cell activation, proliferation, and cytokine production. It contains V-like and C-like immunoglobulin domains. PD-L1 expression is regulated by various cytokines, such as TNF-α or LPS (ISSN: 1848-7718). Increased expression of this protein in certain types of cancers, e.g., renal cell carcinoma or colon cancer, correlates with poor prognosis. What is the molecular weight of PD-L1? Depending on the isoform, the calculated molecular weight of the protein varies between 20 and 33 kDa (176-290 aa). What are the isoforms of PD-L1? According to NCBI, three different isoforms have been identified. There are significant differences in the untranslated and protein coding regions. What is the subcellular localization and tissue specificity of PD-L1? It is predicted to localize in the plasma membrane of various cell types, with a particularly high expression in placental trophoblast and subsets of immune cells. High levels of PD-L1 protein have also been detected in lung and colon tissues. What is the function of PD-L1 in immune responses? PD-L1 is critical for the induction and maintenance of immune self-tolerance during infection or inflammation in normal tissues. The interaction of PD-L1 and its receptors is responsible for preventing auto-immune phenotypes and balancing the overall immune response in situations such as pregnancy or tissue allografts. The interaction between PD-L1 and PD-1 or B7.1 starts an inhibitory signaling cascade, which results in the decreased proliferation of antigen-specific T-cells and increased survival of regulatory T-cells (PMID: 15240681). How can PD-L1's implication in cancer be used as a drug target? In certain tumors, high expression of PD-L1 serves as a stop-sign to inhibit the recognition of cancer cells by T-cells (PMID: 23087408). The interaction between PD-L1 and its receptors (PD1 and B7.1) is a mechanism for the tumor to evade the host immune response (PMID: 29357948). Several mAbs have been developed to target that interaction and thus prevent the inactivation of cytotoxic T-cells by the tumor (PMIDs: 23890059, 18173375).
文献引用 (85)
Conserved spatial subtypes and cellular neighborhoods of cancer-associated fibroblasts revealed by single-cell spatial multi-omics
单细胞空间多组学揭示癌症相关成纤维细胞的保守空间亚型和细胞邻域
A covalent peptide-based lysosome-targeting protein degradation platform for cancer immunotherapy
基于共价肽的溶酶体靶向蛋白质降解平台,用于癌症免疫治疗
CuOTeDsP nanotherapeutics enhance cuproptosis-mediated immunotherapy by modulating cholesterol metabolism in bladder cancer.
CuOTeDsP纳米疗法通过调节膀胱癌中的胆固醇代谢来增强铜凋亡介导的免疫疗法
Ara-C suppresses H3 K27-altered spinal cord diffuse midline glioma growth and enhances immune checkpoint blockade sensitivity.
阿糖胞苷可抑制 H3 K27 改变的脊髓弥漫性中线胶质瘤的生长,并增强免疫检查点阻断的敏感性
Reprogramming tumor-associated macrophages and blocking PD-L1 via engineered outer membrane vesicles to enhance T cell infiltration and cytotoxic functions
通过工程化外膜囊泡重编程肿瘤相关巨噬细胞并阻断PD-L1,以增强T细胞浸润和细胞毒性功能。
Formin protein DAAM1 positively regulates PD-L1 expression via mediating the JAK1/STAT1 axis in pancreatic cancer
福明蛋白 DAAM1 通过介导胰腺癌中的 JAK1/STAT1 轴正向调节 PD-L1 表达
Cinobufagin Inhibits Invasion and Migration of Non-Small Cell Lung Cancer via Regulating Glucose Metabolism Reprogramming in Tumor-Associated Macrophages.
蟾毒灵通过调节肿瘤相关巨噬细胞的葡萄糖代谢重编程来抑制非小细胞肺癌的侵袭和迁移
HKDC1 promotes ovarian cancer progression through boosting lipid metabolism and immune escape by stabilizing G6PC/G6PC2.
HKDC1 通过稳定 G6PC/G6PC2 来促进脂质代谢和免疫逃逸,从而促进卵巢癌的进展
Cryoablation synergizes with anti-PD-1 immunotherapy induces an effective abscopal effect in murine model of cervical cancer.
冷冻消融与抗 PD-1 免疫疗法协同作用,在宫颈癌小鼠模型中诱导有效的远隔效应
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