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宿主来源
Armenian hamster抗原名称
TCR γ/δ分子别名
T cell receptor γ/δ; γ/δ TCR; TCR-γ/δ细胞定位
Cell membraneAccession
P03986, B7Z8K6克隆号
UC7-13D5抗体类型
Recombinant mAb抗体同种型
Armenian hamster IgG同型对照
Invivo Armenian Hamster IgG Isotype Control反应种属 ?
Ms阳性样本
C57BL/6 mouse splenocytes纯化方式
Protein G浓度
3.8 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 pH6,0, Contains no stabilizers or preservatives
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
Functional assays
in vivo cell specific depletion
in vitro cell specific stimulation/activation
FCM
稀释度
应用 稀释度 推荐种属 FCM 1μg per million cells in 100μl volume Ms
The TCR γ/δ protein is a distinctive T-cell receptor (TCR) expressed on the surface of γδ T cells, composed of a γ chain and a δ chain linked by disulfide bonds to form a heterodimer, belonging to the immunoglobulin superfamily. Unlike the conventional αβ TCR, the γδ TCR can directly recognize a broad range of antigens (e.g., phosphorylated metabolites, lipids, stress proteins) without requiring MHC presentation, granting it broader antigen specificity. Its variable (V) region diversity arises from V, (D), and J gene segment rearrangements, though it exhibits less diversity than the αβ TCR. γδ T cells are primarily found in mucosal tissues, skin, and the gut, playing crucial roles in early immune defense, tumor surveillance, and tissue repair. They can rapidly secrete cytokines (e.g., IFN-γ, IL-17) or exert cytotoxic effects, serving as key effector cells bridging innate and adaptive immunity.
流式分析
Flow cytometric analysis of C57BL/6 mouse splenocytes labelling mouse TCR γ/δ antibody at 1/500 dilution (1 μg) / (right panel) compared with an Amenian hamster IgG Isotype Control / (left panel). Goat Anti-Amenian hamster IgG Alexa Fluor® 488 was used as the secondary antibody. Then cells were stained with CD3 - Brilliant Violet 421™ antibody separately. Flow cytometry and data analysis were performed using Agilent NovoCyte Quanteon and FlowJo™ software. Total viable cells, as determined by Fixable Viability Dye 662 (S0D0016), were used for analysis.







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