Anti-PD-L1 antibody [28-8] (Ab205921)
CD274, B7H1, PDCD1L1, PDCD1LG1, PDL1, Programmed cell death 1 ligand 1, PD-L1, PDCD1 ligand 1, Programmed death ligand 1, hPD-L1, B7 homolog 1, B7-H1
详细信息
背景信息
Anti-PD-L1 antibody [28-8] (ab205921) was developed by Abcam using patented rabbit monoclonal antibody technology and is validated for use in Flow Cyt, ICC/IF, IHC-Fr, IHC-P, WB, mIHC in human samples. Anti-PD-L1 antibody [28-8] (ab205921) has been cited over 476 times in peer reviewed journals and is trusted by the scientific community. Abcam's high quality manufacturing and validation processes ensure Anti-PD-L1 antibody [28-8] (ab205921) has high sensitivity and specificity alongside high lot-to-lot consistency and reproducibility. The specificity of Anti-PD-L1 antibody [28-8] (ab205921) has been confirmed by testing in knockout samples. Anti-PD-L1 antibody [28-8] (ab205921) has 13 independent reviews from customers. Anti-PD-L1 antibody [28-8] (ab205921) specifically detects PD-L1 (UniProt ID: Q9NZQ7; Molecular weight: 31kDa) and is sold in a convenient trial size to enable initial testing (20 µL) and larger sizes for subsequent scaling up experiments (50 µL). Conjugation-ready, carrier free format available for antibody clone 28-8 - ab228413. Antibody clone 28-8 is also available pre-conjugated to a variety of labels for your convenience - HRP, PE, Alexa Fluor® 555, Alexa Fluor® 568, Alexa Fluor® 594, FITC ( ab209961, ab209962, ab213358, ab213359, ab213360, ab224027 ). PD-L1 (Programmed Death-Ligand 1) is a protein that plays a significant role in oncology, particularly in the immune response to cancer. It is expressed on the surface of cancer cells and interacts with the PD-1 receptor on T-cells, effectively inhibiting the immune system's ability to attack the tumor. This interaction is a key target for immunotherapy drugs, such as checkpoint inhibitors, which block the PD-1/PD-L1 pathway, allowing the immune system to recognize and destroy cancer cells. FURTHER INFORMATION ON POSITIVE CONTROLS ( Chinese version ) Tissue - Tonsil - with hyperreactive changes. Screening of hyper-reactive tonsils is recommended to find tonsil with the highest expression of PD-L1 in crypt epithelium, macrophages homing the germinal centers and interfollicular mononuclear leukocytes. - Tumor tissues - prescreened for positive tumor and inflammatory infiltrates. PD-L1 expression varies by tumor type so screening is recommended to find positive and negative tumor controls. - The following publication is useful for finding suitable tumor types for PD-L1 expression http://www.immunotherapyofcancer.org/content/1/S1/P53 - Note: Look for specimens with high numbers of inflammatory macrophages and mononuclear leukocytes. Cell Lines - Positive controls: B-CPAP (high), ES-2 (medium), HCC70 (low). Primary antibody negative control: Recombinant Rabbit IgG isotype control antibody, ab172730. Recombinant protein positive control: Recombinant human PD-L1 protein, ab167713. Immunohistochemistry usage For IHC usage on FFPE tissues, we recommend using PD-L1 IHC panel ab236676, which contains PD-L1 antibody clone 28-8 (ab205921), HIER antigen retrieval reagent ( ab208572 ) and IHC detection kit HRP/DAB ( ab209101 ). Western blot usage For clone 28-8, it is recommended to use Odyssey system. This system has the advantages of a wider dynamic range and less background than chemiluminescence. This PD-L1 antibody [28-8] has been used as detector antibody in Human PD-L1 SimpleStep ELISA ® kit: ab214565 and ab277712. To support you in your biomarker discovery and validation studies, we offer a comprehensive suite of solutions including high quality, validated recombinant antibodies and assay kits. Patented technology Our RabMAb ® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb ® patents. What are the advantages of a recombinant monoclonal antibody? This product is a recombinant monoclonal antibody, which offers several advantages including - High batch-to-batch consistency and reproducibility - Improved sensitivity and specificity - Long-term security of supply - Animal-free batch production For more information, read more on recombinant antibodies.
文献引用 (510)
Chronic ER Stress Triggers Cell-Surface Chaperones as the Therapeutic Targets of CAR Cells in Acute Myeloid Leukemia.
慢性内质网应激触发细胞表面分子伴侣作为急性髓系白血病 CAR 细胞的治疗靶点。
Engineered Akkermansia muciniphila vesicles for targeted pyroptosis and trained immunity to enhance immunotherapy in hepatocellular carcinoma.
利用工程改造的 Akkermansia muciniphila 囊泡进行靶向细胞焦亡和训练免疫,以增强肝细胞癌的免疫疗法。
Brain-targeting nanoplatform repurposing silymarin for enhanced GBM immunotherapy via synergistic mitochondrial suppression.
利用水飞蓟素靶向大脑,通过协同抑制线粒体来增强胶质母细胞瘤免疫疗法的纳米平台。
Downregulation of HLA Class I Expression through HLA-A DNA Methylation Is Associated with Reduced CD8+ T-cell Infiltration in Cervical Cancer.
HLA-A DNA甲基化导致HLA I类表达下调与宫颈癌中CD8+ T细胞浸润减少相关。
Construction of circadian clock signature for tumor microenvironment in predicting survival of esophageal squamous cell carcinoma.
构建肿瘤微环境昼夜节律时钟特征以预测食管鳞状细胞癌的生存率。
D-xylose suppresses hepatocellular carcinoma progression by regulating dihydrodiol dehydrogenase and remodeling the immune microenvironment.
D-木糖通过调节二氢二醇脱氢酶和重塑免疫微环境来抑制肝细胞癌的进展。
PEAK1 promotes prostate cancer progression and docetaxel resistance by mediating the polarization of tumor-associated macrophages.
PEAK1 通过介导肿瘤相关巨噬细胞的极化,促进前列腺癌的进展和多西他赛耐药性。
Muscle expression of PD1 and PD-L1 may predict the severity and outcomes of neuromuscular immune-related adverse events caused by immune checkpoint inhibitor treatment.
肌肉中 PD1 和 PD-L1 的表达可能预测免疫检查点抑制剂治疗引起的神经肌肉免疫相关不良事件的严重程度和结果。
Plant-nanoparticles enhance anti-PD-L1 efficacy by shaping human commensal microbiota metabolites
植物纳米颗粒通过调控人体共生微生物代谢物来增强抗PD-L1疗效
PD-L1-Targeting Biomimetic Photoresponsive Thermosensitive Liposomes for Triple-Negative Breast Cancer.
用于治疗三阴性乳腺癌的PD-L1靶向仿生光响应热敏脂质体。
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