APC Mouse Anti-Human CD62L Antibody (S-937-77)
L-selectin,CD62 antigen-like family member L,Leukocyte adhesion molecule 1 (LAM-1),Leukocyte surface antigen Leu-8,Leukocyte-endothelial cell adhesion molecule 1 (LECAM1),Lymph node homing receptor,LNHR,LYAM1,SELL
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宿主来源
Mouse抗原名称
CD62L分子别名
L-selectin; CD62 antigen-like family member L; Leukocyte adhesion molecule 1 (LAM-1); Leukocyte surface antigen Leu-8; Leukocyte-endothelial cell adhesion molecule 1 (LECAM1); Lymph node homing receptor; LNHR; LYAM1; SELL细胞定位
Cell membraneAccession
P14151克隆号
S-937-77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
0.1 mg/ml标记
APC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 2μl per million cells in 100μl volume Hu
CD62L, also known as L-selectin, is a type-I transmembrane glycoprotein and cell adhesion molecule belonging to the selectin family, primarily expressed on the surface of leukocytes, including T cells, B cells, and natural killer cells. It plays a crucial role in leukocyte homing and immune cell localization by mediating the initial rolling and adhesion of white blood cells to endothelial cells during inflammation. CD62L is also a marker for central memory T cells, which have a higher expression level of this molecule, allowing them to quickly respond to antigen re-exposure. Additionally, CD62L is involved in the regulation of immune cell distribution in tissues, impacting the strength and duration of immune responses. In cancer therapy, manipulating CD62L expression can enhance T cell infiltration into the tumor microenvironment, improving the efficacy of immunotherapy.
流式分析
Flow cytometric analysis of Human CD62L expression on human PBMC (human peripheral blood mononuclear cells). Human PBMC were stained with Brilliant Violet 421™ Mouse Anti-Human CD4 Antibody and either APC Mouse IgG1, κ Isotype Control (Left panel) or SDT APC Mouse Anti-Human CD62L Antibody (Right panel) at 2μl/test. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.







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