Flow cytometric analysis of Mouse CD80 expression on C57BL/6 mouse splenocytes treated with ConA. C57BL/6 mouse splenocytes (Left panel) or treated 72h with 2.5μg/ml Concanavalin A (Right panel) were stained with Brilliant Violet 421™ Rat Anti-Mouse CD4 and SDT Biotin Rat Anti-Mouse PD-L1 Antibody at 5 μl/test followed by Sav-PE. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.
Product Details
Product Details
Product Specification
| Host | Rat |
| Antigen | PD-L1 |
| Synonyms | Programmed cell death 1 ligand 1; PDCD1 ligand 1; Programmed death ligand 1; B7 homolog 1 (B7-H1); B7h1; Pdcd1l1; Pdcd1lg1; Pdl1; Cd274 |
| Location | Endosome, Cell membrane |
| Accession | Q9EP73 |
| Clone Number | S-R072 |
| Antibody Type | Rat mAb |
| Isotype | IgG2b |
| Application | FCM |
| Reactivity | Ms |
| Positive Sample | ConA treated with C57BL/6 mouse splenocytes |
| Purification | Protein G |
| Concentration | 0.2 mg/ml |
| Conjugation | Biotin |
| Physical Appearance | Liquid |
| Storage Buffer | PBS pH7.4, 0.03% Proclin 300 |
| Stability & Storage | 12 months from date of receipt / reconstitution, 2 to 8 °C as supplied |
Dilution
| application | dilution | species |
| FCM | 5μl per million cells in 100μl volume | Ms |
Background
PD-L1 (Programmed Death-Ligand 1, CD274, B7-H1) is a ~33 kDa type I trans-membrane glycoprotein that belongs to the B7 family of immune co-signaling molecules; it is expressed constitutively at low levels on resting T, B, and myeloid-lineage cells and is strongly up-regulated by pro-inflammatory cytokines such as IFN-γ, TNF-α, IL-4, GM-CSF and by oncogenic signaling pathways (EGFR, ALK, KRAS, PI3K-AKT, STAT3, HIF-1α, NF-κB) in a wide spectrum of epithelial, hematopoietic, and mesenchymal tumors. Upon engagement with its cognate inhibitory receptor PD-1 (CD279) expressed on activated T, B, and NK cells, PD-L1 delivers a negative signal that recruits SHP-1/2 phosphatases to the immunological synapse, thereby blocking PI3K-AKT and ZAP70 signaling, suppressing T-cell proliferation, cytokine production (IL-2, IFN-γ, TNF-α, granzyme B), and survival while promoting the induction and maintenance of peripheral tolerance, tissue-resident T-cell exhaustion, and Treg expansion. Clinically, PD-L1 protein expression—detected by FDA-approved 22C3, 28-8, SP142, or SP263 IHC assays—is a predictive biomarker for anti-PD-1/PD-L1 checkpoint inhibitors used across more than 20 cancer types, with high membranous tumor and/or immune cell staining (≥1–50 % cutoff depending on tumor type) correlating with improved objective response rates and progression-free survival; conversely, PD-L1 overexpression is itself an independent adverse prognostic factor in untreated solid tumors, reflecting immune evasion and aggressive biology.
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