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宿主来源
Mouse抗原名称
CD11c分子别名
Integrin alpha-X; CD11 antigen-like family member C; Leu M5; Leukocyte adhesion glycoprotein p150/95 alpha chain; Leukocyte adhesion receptor p150/95; ITGAX细胞定位
Cell membraneAccession
P20702克隆号
S-R424抗体类型
Mouse mAb抗体同种型
IgG1,k反应种属 ?
Hu阳性样本
human PBMC纯化方式
Protein G浓度
0.05mg/ml标记
FITC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 5 μl per million cells in 100μl volume Hu
CD11c is a type I transmembrane glycoprotein of approximately 150 kDa, also known as integrin alpha X (Itgax). It is part of the complement receptor 4 (CR4) complex and, along with CR3 (also known as Mac-1 or CD11b/CD18), belongs to the β2-integrin family of adhesion molecules. CD11c is primarily expressed on dendritic cells (DCs), NK cells, a subset of intestinal intraepithelial lymphocytes (IELs), and some activated T cells. It is involved in cell adhesion, migration, and phagocytic functions, mediating the phagocytic process of DCs through its association with β2-integrin. Under conditions of early development and in certain neurodegenerative diseases such as Alzheimer's disease (AD), a subset of microglia in the central nervous system also expresses CD11c. CD11c+ microglia express genes such as Spp1, which encodes osteopontin (OPN), a cytokine-like phosphorylated protein involved in pathogenic and protective immune responses in peripheral lymphoid tissues. Additionally, CD11c serves as a marker for macrophages, whose expression aids researchers in identifying and characterizing these cells, thus contributing to a deeper understanding of their roles in immune and inflammatory processes.
流式分析
Flow cytometric analysis of Human CD11c expression on human PBMC (human peripheral blood mononuclear cell). Human PBMC were stained with Brilliant Violet 510™ Mouse Anti-Human CD14 antibody and either FITC Mouse IgG1, κ Isotype Control (Left panel) or SDT FITC Mouse Anti-Human CD11c Antibody (Right panel) at 0.25 μg/test. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.







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