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宿主来源
Mouse抗原名称
CD45分子别名
Receptor-type tyrosine-protein phosphatase C; Leukocyte common antigen (L-CA); T200; Ptprc细胞定位
Cell membrane, SynapseAccession
P04157克隆号
OX-1抗体类型
Mouse mAb抗体同种型
IgG1,k反应种属 ?
Rt阳性样本
Wistar Rat splenocytes纯化方式
Protein G浓度
0.2 mg/ml标记
Pacific Blue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 1.25μl per million cells in 100μl volume Rt
CD45, also known as protein tyrosine phosphatase receptor type C (PTPRC) or leukocyte common antigen, is a transmembrane glycoprotein expressed on nearly all hematopoietic cells and plays a crucial role in the regulation of T and B cell antigen receptor-mediated activation. It is a type 1 transmembrane protein tyrosine phosphatase (PTPase) that is involved in the activation, development, tolerance, and survival of T and B-lymphocytes. CD45 is essential for the initiation of T cell receptor (TCR) signaling and modulates cytokine and chemokine production and signaling. It also negatively regulates monocytic cell differentiation and FLT3 signaling in vivo. The protein is involved in the nuclear apoptosis process and is vital for chromatin condensation and DNA fragmentation. Furthermore, CD45 is implicated in the interaction between T cells and macrophages and has been studied as a therapeutic target for immune diseases, including autoimmunity and organ transplantation. Disruption of the equilibrium between protein tyrosine kinase and phosphatase activity, which includes CD45, can result in immunodeficiency, autoimmunity, or malignancy.
流式分析
Flow cytometric analysis of Rat CD45 expression on Wistar Rat splenocytes. Wistar Rat splenocytes were stained with either Pacific Blue Mouse IgG1, κ Isotype Control (Black line histogram) or SDT Pacific Blue Mouse Anti-Rat CD45 Antibody (Red line histogram) at 1.25μl/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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