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宿主来源
Mouse抗原名称
Siglec-10分子别名
Sialic acid-binding Ig-like lectin 10; SLG2; SIGLEC10细胞定位
Secreted, Cell membraneAccession
Q96LC7克隆号
S-4483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
0.2 mg/ml标记
Biotin性状
Liquid缓冲体系
PBS pH7.4, 0.03% 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 5μl per million cells in 100μl volume Hu
Siglec-10 (Sialic acid-binding Ig-like lectin 10) is an inhibitory immune checkpoint receptor primarily expressed on the surface of human myeloid cells, including monocytes, macrophages, and dendritic cells, which plays a critical role in maintaining immune tolerance and preventing excessive inflammation. Structurally characterized by an N-terminal V-set Ig-like domain that specifically recognizes sialic acid residues on glycan chains, Siglec-10 transmits negative regulatory signals upon ligand binding through its cytoplasmic immunoreceptor tyrosine-based inhibitory motifs (ITIMs) and ITIM-like sequences, thereby recruiting phosphatases such as SHP-1 and SHP-2 to dampen downstream activating signaling pathways. This receptor is notably involved in distinguishing self from non-self by interacting with "self-associated molecular patterns" (SAMPs), a mechanism that suppresses immune responses against healthy host tissues but can be co-opted by tumors to evade immune surveillance; consequently, blocking the interaction between Siglec-10 and its sialylated ligands has emerged as a promising therapeutic strategy in cancer immunotherapy to reactivate anti-tumor immunity, while its dysfunction is also implicated in various inflammatory disorders and infectious diseases where pathogen mimicry of host glycans exploits this inhibitory pathway.
流式分析
Flow cytometric analysis of human Siglec-10 expression on human PBMC. Human PBMC were stained with APC Mouse Anti-Human CD19 Antibody and either Biotin Isotype Control (left panel) or SDT Biotin Mouse Anti-Human Siglec-10 Antibody (right panel) at 5μl/test followed by Sav-PE. Total viable cells, as determined by Fixable Viability Dye 452 (S0D0021), were used for analysis. Flow cytometry and data analysis were performed using Agilent NovoCyte Quanteon and FlowJo™ software.







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