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宿主来源
Mouse抗原名称
CD49a分子别名
Integrin alpha-1; CD49 antigen-like family member A; Laminin and collagen receptor; VLA-1; ITGA1细胞定位
MembraneAccession
P56199克隆号
S-5297抗体类型
Mouse mAb抗体同种型
IgG1,k同型对照
S0B5431反应种属 ?
Hu阳性样本
HeLa纯化方式
Protein G浓度
0.2 mg/ml标记
Biotin性状
Liquid缓冲体系
PBS pH7.4, 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
CD49a, also known as integrin α1 subunit or the α chain of VLA-1, is a transmembrane glycoprotein encoded by the ITGA1 gene. It is an important member of the integrin family, forming the α1β1 integrin complex through non-covalent association with the β1 subunit (CD29), serving as a cell surface receptor for collagen and laminin. This protein is expressed on various cell types, including activated T cells, monocytes, smooth muscle cells, and endothelial cells, with its extracellular domain containing a critical I-type domain that mediates cell adhesion to collagen and laminin in the extracellular matrix. Beyond its fundamental adhesive functions, CD49a has recently been established as a key marker for tissue-resident memory T cells (TRM) and type 1 innate lymphoid cells (ILC1), among other tissue-resident immune cell populations. Under inflammatory or infectious conditions, it is induced and upregulated by cytokines such as TGF-β and IL-12, promoting the long-term survival of CD8⁺ TRM cells in peripheral tissues like the skin and maintaining their dendritic morphology to facilitate local immune surveillance, while also participating in regulating the migration and function of uterine natural killer (uNK) cells. Furthermore, aberrant CD49a expression is associated with various pathological conditions, including fibrosis, inflammatory diseases, as well as tumor progression and drug resistance, making it a potential therapeutic intervention target.
流式分析
Flow cytometric analysis of CD49a expression on HeLa (Human cervix adenocarcinoma epithelial cell, right) / Raji (Human Burkitt's lymphoma B lymphocyte, left). HeLa cells and Raji cells were stained with either Biotin Mouse IgG1, k Isotype Control (black line histogram) or SDT Biotin Mouse Anti-Human CD49a Antibody (red line histogram) at 5 μl/test followed by Sav-iFluor 488, 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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