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宿主来源
Rabbit抗原名称
CD43分子别名
Leukosialin; GPL115; Galactoglycoprotein (GALGP); Leukocyte sialoglycoprotein; Sialophorin; SPN细胞定位
MembraneAccession
P16150克隆号
S-R101抗体类型
Recombinant mAb抗体同种型
IgG同型对照
S0B0161反应种属 ?
Hu阳性样本
Human PBMC纯化方式
Protein A浓度
0.2 mg/ml标记
Alexa Fluor® 488性状
Liquid缓冲体系
PBS, 1% BSA, 0.09% sodium azide
储存条件
12 months from date of receipt / reconstitution, 2 to 8 °C as supplied
应用
ICFCM
稀释度
应用 稀释度 推荐种属 ICFCM 5μl per million cells in 100μl volume Hu
CD43, also known as Leukosialin or Sialophorin, is a type I transmembrane glycoprotein that is highly expressed on the surface of leukocytes (such as T cells, monocytes, and granulocytes) but is absent on resting naive B cells and erythrocytes. Structurally, it features a unique, negatively charged, rigid rod-like extracellular domain heavily modified by approximately 80 O-glycans, along with a cytoplasmic tail containing potential phosphorylation sites that can interact with cytoskeletal linker proteins (such as ERM family members). Functionally, CD43 plays a dual role as both an "anti-adhesion" molecule and a signaling regulator: its bulky extracellular domain serves as a physical barrier that negatively regulates integrin- and L-selectin-mediated cell adhesion and homing through steric hindrance, while its cytoplasmic domain transmits signals to finely regulate T cell activation, proliferation, apoptosis, and the contraction of immune responses. Furthermore, dysregulation of CD43 is closely associated with disease—it is defective or absent in patients with Wiskott-Aldrich syndrome. In various cancer cells, such as acute myeloid leukemia, highly expressed CD43 and its surface sialylated glycosylation modifications form a "glyco-immune barrier" that physically impedes contact between immune effector cells (including macrophages and NK cells) and tumor cells, thereby helping cancer cells achieve immune evasion. Given its central role in immune regulation and tumor immune escape, CD43 has emerged as a highly promising novel target for cancer immunotherapy.
流式分析
Flow cytometric analysis of Human PBMC fixed with 4% paraformaldehyde and permeabilized with 0.1% Tween. Cells were stained with Brilliant Violet 421™ Mouse anti-human CD3 Antibody (right panel) and either Alexa Fluor® 488 Rabbit IgG Isotype Control (left panel) or Alexa Fluor® 488 Rabbit Anti-Human CD43 Antibody (right panel) at 5 μl/test. Total viable cells, as determined by Fixable Viability Dye 662 (S0B88806), were used for analysis. Flow cytometry and data analysis were performed using Agilent NovoCyte Quanteon and FlowJo™ software.







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