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宿主来源
Mouse抗原名称
CD1a分子别名
T-cell surface glycoprotein CD1a; T-cell surface antigen T6/Leu-6 (hTa1 thymocyte antigen)细胞定位
Cell membraneAccession
P06126克隆号
S-R527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
MOLT-4纯化方式
Protein G浓度
0.02mg/ml标记
PE-Cy7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 | 稀释度 | 推荐种属 |
---|---|---|
FCM | 5 μl per million cells in 100μl volume | Hu |
CD1a is a cell surface glycoprotein that is part of the CD1 family of antigen-presenting molecules. It is primarily expressed on Langerhans cells, a type of dendritic cell found in the epidermis of the skin, as well as on certain T-cell leukemias and thymocytes. CD1a is involved in the presentation of lipid antigens to T-cells, particularly to a subset of T-cells known as invariant natural killer T (iNKT) cells. CD1a plays a crucial role in immune responses, particularly in the initiation and amplification of local and systemic events during skin inflammation. It has been shown that CD1a can capture endogenous cellular lipids that broadly block T cell responses, suggesting its role in regulating immune reactions. In conditions such as atopic dermatitis and psoriasis, CD1a expression and reactivity have been linked to disease pathology. Moreover, CD1a has been implicated in the pathogenesis of various diseases, including mycobacterial infections and certain types of cancer. It can serve as a biomarker for disease diagnosis, monitoring, and personalized treatment strategies.
流式分析
Flow cytometric analysis of CD1a expression on MOLT-4 cells. Cells from the Human MOLT-4 (Human lymphoblastic leukemia T lymphoblast, Right) or HeLa (Human cervix adenocarcinoma epithelial cell, Left) cell line were stained with PE-Cy7 Mouse IgG1, κ Isotype Control (Black line histogram) and SDT PE-Cy7 Mouse Anti-Human CD1a antibody (Red line histogram) at 0.1 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.
实验方案
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