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宿主来源
Rat抗原名称
Thy1 (CD90)分子别名
Thy-1 membrane glycoprotein; Thy-1 antigen; Thy-1细胞定位
Cell membraneAccession
P01831克隆号
S-4038抗体类型
Rat mAb抗体同种型
IgG2a反应种属 ?
Ms阳性样本
C57BL/6 mouse splenocytes纯化方式
Protein G浓度
0.5 mg/ml标记
Alexa Fluor® 488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 1μg per million cells in 100μl volume Ms
Thy1 (also known as CD90) is a glycosylphosphatidylinositol (GPI)-anchored glycoprotein widely expressed on the surface of various cell types and belongs to the immunoglobulin superfamily; it was originally named after its discovery in mouse thymocytes. As a critical marker for stem cells and specific differentiated cells, Thy1 is highly expressed on hematopoietic stem cells, mesenchymal stem cells (MSCs), neurons, fibroblasts, and activated T cells, with its functions varying significantly depending on the cell type: in the nervous system, it participates in axon growth, synaptic plasticity, and neural repair; in the immune system, it regulates T cell activation, adhesion, and migration; and in stem cell research, it serves as a key surface antigen for identifying and isolating MSCs (typically characterized as CD90-positive). Although its precise downstream signaling mechanisms remain not fully understood due to the lack of a transmembrane domain, Thy1 is generally believed to mediate cell-cell and cell-matrix adhesion by interacting with extracellular matrix components or other membrane proteins, thereby influencing cell proliferation, differentiation, and tissue homeostasis, making it a vital target in regenerative medicine, neurobiology, and oncology.
流式分析
Flow cytometric analysis of mouse Thy1(CD90) expression on C57BL/6 mouse splenocytes. C57BL/6 mouse splenocytes were stained with Brilliant Violet 421™ Rat Anti-Mouse CD3 Antibody and either Alexa Fluor® 488 Rat IgG2a Isotype Control (left panel) or SDT Alexa Fluor® 488 Rat Anti- Mouse Thy1(CD90) Antibody (right panel) at 2 μl/test. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.







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