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宿主来源
Rat抗原名称
CD86/B7-2分子别名
T-lymphocyte activation antigen CD86; Activation B7-2 antigen; Early T-cell costimulatory molecule 1 (ETC-1); Cd86细胞定位
Cell membraneAccession
P42082克隆号
GL-1抗体类型
Rat mAb抗体同种型
Rat IgG2a,k同型对照
Invivo rat IgG2a isotype control, anti-trinitrophenol反应种属 ?
Ms阳性样本
BALB/c mouse splenocytes纯化方式
Protein G浓度
5 mg/ml纯度
>95%(Determined by SDS-PAGE)内毒素含量
<1EU/mg标记
Unconjugated性状
Liquid缓冲体系
PBS pH7.4, containing no preservative
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
in vivo CD86 blockade
FCM
稀释度
应用 稀释度 推荐种属 FCM 1:500 Ms
CD86, also historically referred to as B7-2, is a type I transmembrane protein belonging to the immunoglobulin superfamily that serves as a critical costimulatory molecule primarily expressed on the surface of professional antigen-presenting cells (APCs) such as dendritic cells, macrophages, and B cells. Functioning as a ligand for the CD28 and CTLA-4 (CD152) receptors on T cells, CD86 plays a pivotal role in regulating the adaptive immune response by providing the necessary "second signal" required for naive T cell activation, proliferation, and differentiation upon engagement with CD28, while its interaction with CTLA-4 delivers an inhibitory signal that helps maintain immune tolerance and prevent autoimmunity. Although it shares functional redundancy with its counterpart CD80 (B7-1), CD86 is typically constitutively expressed at low levels and is upregulated more rapidly than CD80 following APC activation, making it the dominant costimulatory molecule during the early phases of immune responses, which underscores its significance as a therapeutic target in various clinical contexts, including cancer immunotherapy, autoimmune diseases, and transplant rejection management.
流式分析
Flow cytometric analysis of CD86/B7-2 expression in BALB/c mouse splenocytes. Mouse splenocytes were treated with 500ng/ml LPS for 3 days (right panel) or untreatred (left panel) and labeled with CD86/B7-2 antibody at 1/500 dilution (1 μg). Goat Anti-Rat 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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