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宿主来源
Mouse抗原名称
CD272分子别名
B- and T-lymphocyte attenuator; B- and T-lymphocyte-associated protein; BTLA细胞定位
Cell membraneAccession
Q7Z6A9克隆号
MIH26抗体类型
Mouse mAb抗体同种型
IgG2a,k反应种属 ?
Hu阳性样本
human PBMC纯化方式
Protein A浓度
0.2 mg/ml标记
Alexa Fluor® 647性状
Liquid缓冲体系
PBS, 1% BSA, 0.09% sodium azide
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 Hu
CD272, also known as B- and T-lymphocyte attenuator (BTLA), is a member of the CD28 immunoglobulin superfamily and functions as a co-inhibitory receptor. It is a transmembrane glycoprotein with structural similarities to PD-1 and CTLA-4, consisting of an extracellular domain, a transmembrane domain, and a cytoplasmic domain that contains motifs crucial for signaling. BTLA is encoded by the BTLA gene and is broadly expressed in various immune organs and cells, including lymph nodes, thymus, spleen, T cells, B cells, dendritic cells, and NKT cells. Its expression fluctuates depending on the developmental stage of the cells. For instance, in T cells, BTLA is stably expressed in naive T cells, increases upon stimulation, and decreases after full activation. BTLA interacts with its ligand, herpes virus entry mediator (HVEM), which belongs to the tumor necrosis factor receptor superfamily. This interaction negatively regulates T cell proliferation and cytokine production through the phosphorylation of immunoreceptor tyrosine-based inhibitory motifs (ITIMs) and the binding of SHP-1/SHP-2. BTLA plays a role in maintaining immune homeostasis and has potential applications in the regulation of immune responses in diseases such as cancer and autoimmune disorders.
流式分析
Flow cytometric analysis of human CD272 expression on human PBMC (human peripheral blood mononuclear cell). Human PBMC were stained with Brilliant Violet 421™ Mouse Anti-Human CD3 Antibody and either Alexa Fluor® 647 Mouse IgG2a, k Isotype Control (left panel) or SDT Alexa Fluor® 647 Mouse Anti-Human CD272 Antibody (right panel) at 5 μl/test. Flow cytometry and data analysis were performed using Agilent NovoCyte Quanteon and FlowJo™ software.







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