Alexa Fluor® 647 Mouse Anti-Rat CD161 Antibody (S-R628)
Killer cell lectin-like receptor subfamily B member 1A,NKR-P1A,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
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宿主来源
Mouse抗原名称
CD161分子别名
Killer cell lectin-like receptor subfamily B member 1A; NKR-P1A; 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细胞定位
MembraneAccession
P27471克隆号
S-R628抗体类型
Mouse mAb抗体同种型
IgG1,k反应种属 ?
Rt阳性样本
SD Rat splenocytes纯化方式
Protein G浓度
0.02mg/ml标记
Alexa Fluor® 647性状
Liquid缓冲体系
PBS, 1% BSA, 0.3% Proclin 300储存条件
12 months from date of receipt / reconstitution, 2 to 8 °C as supplied.
应用
FCM
稀释度
应用 稀释度 推荐种属 FCM 5μl per million cells in 100μl volume Rt
CD161, also known as KLRB1 or NKRP1A, is a C-type lectin-like receptor primarily expressed on the surface of natural killer (NK) cells and a subset of T cells, including mucosal-associated invariant T (MAIT) cells and some CD8+ T cells. It is particularly enriched in immune cells located in mucosal sites such as the gut and liver. CD161 binds to its ligand, lectin-like transcript 1 (LLT1, also known as CLEC2D), and this interaction can have both inhibitory and costimulatory effects on immune cells. In the context of cancer immunotherapy, CD161 has been identified as a potential inhibitory receptor in glioma-infiltrating T cells. Its activation by CLEC2D on tumor or immunosuppressive cells can dampen T cell responses against cancer cells. Recent studies suggest that blocking the CD161-CLEC2D interaction may enhance T cell-mediated antitumor activity, making CD161 a promising target for cancer immunotherapy.
流式分析
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® 647 Mouse IgG1, κ Isotype Control (Left panel) or SDT Alexa Fluor® 647 Mouse Anti-Rat CD161 Antibody (Right panel) at 5μl/test. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.







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