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宿主来源
Mouse抗原名称
CD152(CTLA-4)分子别名
Cytotoxic T-lymphocyte protein 4; Cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4); CTLA4细胞定位
Cell membraneAccession
P16410克隆号
BN13抗体类型
Mouse mAb抗体同种型
IgG2a,k同型对照
Invivo mouse IgG2a isotype control反应种属 ?
Hu阳性样本
PHA-activated human PBMC纯化方式
Protein A浓度
5 mg/ml标记
Unconjugated性状
Liquid缓冲体系
PBS pH7.4
储存条件
2 to 8 °C for 2 weeks under sterile conditions;
-20 °C for 3 months under sterile conditions;
-80 °C for 24 months under sterile conditions.
Please avoid repeated freeze-thaw cycles.应用
ICFCM
in vitro neutralization
稀释度
应用 稀释度 推荐种属 FCM 1:500 Hu
CD152 is a 223-amino-acid transmembrane glycoprotein receptor expressed mainly on activated CD4+ and CD8+ T cells that functions as a critical negative regulator of immune responses by out-competing CD28 for binding to the costimulatory ligands CD80 (B7-1) and CD86 (B7-2) on antigen-presenting cells, thereby transducing inhibitory signals that attenuate T-cell proliferation, cytokine production, and cell cycle progression; the protein’s signal peptide is cleaved to yield a disulfide-linked homodimer whose extracellular Ig-like V-type domain mediates high-avidity ligand engagement, while its cytoplasmic tail contains a tyrosine-based motif that recruits phosphatases such as SHP-2 and PP2A to propagate inhibitory cascades, and genetic polymorphisms or therapeutic blockade of CD152 (e.g., the monoclonal antibody ipilimumab) can enhance antitumor immunity but also precipitate autoimmune toxicities, underscoring its pivotal role in maintaining immune homeostasis.
流式分析
Flow cytometric analysis of CD152 expression in activated human PBMC (human peripheral blood mononuclear cell). PHA-activated (2 days) human PBMC (right panel) or unstimulated (left Panel) were fixed with 4% PFA and permeabilization with the 0.1% Tween. Then cells were labeled with Human CD152 antibody at 1/500 dilution (1 μg). Goat Anti-Mouse IgG Alexa Fluor® 647 was used as the secondary antibody. Then cells were stained with Brilliant Violet 421™ Mouse Anti-Human CD3 antibody. Flow cytometry and data analysis were performed using Agilent NovoCyte Quanteon and FlowJo™ software.







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