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宿主来源
Mouse抗原名称
CD11a分子别名
Integrin alpha-L; CD11 antigen-like family member A; Leukocyte adhesion glycoprotein LFA-1 alpha chain (LFA-1A); Leukocyte function-associated molecule 1 alpha chain; ITGAL细胞定位
Cell membraneAccession
Q9UQ88克隆号
S-R402抗体类型
Mouse mAb抗体同种型
IgG1,k应用
FCM反应种属 ?
Hu阳性样本
Human PBMC纯化方式
Protein G浓度
0.1mg/ml标记
Pacific Blue性状
Liquid缓冲体系
PBS, 25% Glycerol, 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 | 稀释度 | 推荐种属 |
---|---|---|
FCM | 5 μl per million cells in 100μl volume | Hu |
CD11a, also known as Lymphocyte Function-Associated Antigen 1 (LFA-1) alpha chain or integrin alpha L, is an adhesion molecule primarily expressed on leukocytes such as Leu[A5] cells. It plays a crucial role in cellular adhesion by binding to intercellular adhesion molecules (ICAMs) like ICAM-1 (CD54), ICAM-2 (CD102), and ICAM-3 (CD105). Additionally, CD11a can interact with JAM-1, facilitating the passage of leukocytes across endothelial cells. CD11a has various functions in the immune system. For instance, in primary immune thrombocytopenia (ITP), CD11a is expressed on regulatory T cells (Tregs) and interacts with antigen-presenting cells (APCs) to participate in immune regulation. Furthermore, CD11a is associated with the progression of rheumatoid arthritis (RA) and is considered an important factor in the pathogenesis of the disease. In cancer therapy, CD11a also shows promising potential. Researchers have found that activating molecules like CD11a on the surface of macrophages can enhance their ability to kill cancer cells, providing a hopeful approach for cancer treatment.
流式分析
- Flow cytometric analysis of Human CD11a expression on human peripheral blood mononuclear cell populations. Human peripheral blood mononuclear cell populations were stained with either Pacific blue Mouse IgG1, κ Isotype Control (Black line histogram) or SDT Pacific blue Mouse Anti-Human CD11a antibody (Red line histogram) at 0.5 μg/test, cells without incubation with primary antibody and secondary antibody (Blue line histogram) was used as unlabelled control. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.
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