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宿主来源
Mouse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-4602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
2 mg/ml标记
Unconjugated性状
Liquid缓冲体系
PBS pH7.4
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 1:400 Hu
CD43, also known as leukosialin or sialophorin and encoded by the SPN gene, is a highly glycosylated type I transmembrane sialoglycoprotein predominantly expressed on the surface of most hematopoietic cells, including T lymphocytes, monocytes, macrophages, granulocytes, and platelets, but notably absent on normal resting B cells. Structurally characterized by an extended extracellular domain rich in serine, threonine, and proline residues that are heavily O-glycosylated, CD43 functions primarily as an anti-adhesive molecule due to its large size and negative charge, which creates a steric and electrostatic barrier that prevents non-specific cell-cell interactions and facilitates cell motility during immune surveillance and inflammation. Beyond its physical role in modulating cell adhesion, CD43 acts as a critical signal transduction molecule; upon ligation or cross-linking, it triggers intracellular signaling cascades involving tyrosine kinases such as Lck and Fyn, thereby influencing T-cell activation, proliferation, apoptosis, and cytoskeletal reorganization. Clinically, CD43 serves as an important diagnostic marker in hematopathology, particularly for distinguishing certain T-cell neoplasms and myeloid disorders from B-cell malignancies, while its aberrant expression patterns have also been implicated in various pathological conditions, including autoimmune diseases and cancer metastasis, highlighting its multifaceted role in both physiological immune regulation and disease pathogenesis.
流式分析
Flow cytometric analysis of human PBMC labeled with anti-human CD43 antibody at 1/400 dilution (0.5 μg) / (right panel) compared with a Mouse IgG21, κ Isotype Control / (left panel). Goat Anti-Mouse IgG Alexa Fluor® 488 was used as the secondary antibody. Then cells were stained with CD19 - Brilliant Violet 421™ antibody separately. Flow cytometry and data analysis were performed using Agilent NovoCyte Quanteon and FlowJo™ software.







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