Flow cytometric analysis of rat CD161 expression on SD rat splenocytes. SD rat splenocytes were stained with Alexa Fluor® 488 Mouse Anti-Rat CD3 Antibody and either Alexa Fluor® 700 Mouse IgG1, κ Isotype Control (left panel) or SDT Alexa Fluor® 700 Mouse Anti-Rat CD161 Antibody (right panel) at 2 μl/test. Flow cytometry and data analysis were performed using Agilent NovoCyte Quanteon and FlowJo™ software.
Product Details
Product Details
Product Specification
| Host | Mouse |
| Antigen | CD161 |
| Synonyms | Killer cell lectin-like receptor subfamily B member 1A; Antigen 3.2.3; CD161 antigen-like family member A; Natural killer cell surface protein P1-3.2.3 (NKR-P1 3.2.3); CD161a; Nkrp1a; Klrb1a |
| Location | Membrane |
| Accession | P27471 |
| Clone Number | S-R628 |
| Antibody Type | Mouse mAb |
| Isotype | IgG1,k |
| Application | FCM |
| Reactivity | Rt |
| Positive Sample | SD rat splenocytes |
| Purification | Protein G |
| Concentration | 0.5 mg/ml |
| Conjugation | Alexa Fluor® 700 |
| Physical Appearance | Liquid |
| Storage Buffer | PBS, 1% BSA, 0.09% sodium azide |
| Stability & Storage | 12 months from date of receipt / reconstitution, 2 to 8 °C as supplied |
Dilution
| application | dilution | species |
| FCM | 1μg per million cells in 100μl volume | Rt |
Background
CD161, also known as Natural Killer Cell Receptor P1B (NKR-P1B) or CLEC2D, is a type II transmembrane glycoprotein belonging to the C-type lectin-like receptor superfamily that plays a pivotal role in modulating immune responses, particularly within the context of innate and adaptive immunity. Primarily expressed on natural killer (NK) cells, NKT cells, and specific subsets of T cells—including Th17 cells and mucosal-associated invariant T (MAIT) cells—CD161 functions by binding to its endogenous ligand, LLT1 (lectin-like transcript 1), which is often upregulated on activated antigen-presenting cells and certain tumor cells. This interaction generally delivers an inhibitory signal that dampens cytotoxicity and cytokine production, thereby serving as a critical checkpoint to prevent excessive immune activation and autoimmunity; however, depending on the cellular context and co-stimulatory signals, it can also influence cell migration and tissue retention, making CD161 a significant biomarker for identifying pro-inflammatory T cell subsets involved in autoimmune diseases such as multiple sclerosis and rheumatoid arthritis, as well as a potential therapeutic target in cancer immunotherapy where blocking this axis could enhance anti-tumor immune effector functions.
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