Flow cytometric analysis of SD Rat splenocytes labelling TCR γ/δ antibody at 1/200 dilution (1 μg) / (Right panel) compared with a Mouse IgG1, κ Isotype Control / (Left panel). Goat Anti-Mouse IgG Alexa Fluor® 488 was used as the secondary antibody. Then cells were stained with CD3 - PE Antibody separately.
Product Details
Product Details
Product Specification
| Host | Mouse |
| Antigen | TCR γ/δ |
| Location | Cell membrane |
| Accession | A0A8I6G2Y5 |
| Clone Number | S-3864 |
| Antibody Type | Mouse mAb |
| Isotype | IgG1,k |
| Application | FCM |
| Reactivity | Rt |
| Positive Sample | SD Rat splenocytes |
| Purification | Protein G |
| Concentration | 2 mg/ml |
| Conjugation | Unconjugated |
| Physical Appearance | Liquid |
| Storage Buffer | PBS pH7.4 |
| Stability & Storage | 12 months from date of receipt / reconstitution, 2 to 8 °C as supplied |
Dilution
| application | dilution | species |
| FCM | 1:200 | Rt |
Background
TCR γ/δ protein is a heterodimeric receptor—composed of one γ and one δ chain, each with a variable (V) and constant (C) immunoglobulin-like domain plus a short cytoplasmic tail—whose extracellular V regions recognize phosphoantigens, stress molecules or butyrophilin family ligands without MHC restriction, while its membrane-proximal C regions associate with CD3δε, γε and ζζ signaling modules; upon ligand binding the γ/δ chains undergo conformational change that exposes CD3 ITAMs to Lck-mediated phosphorylation, recruiting ZAP-70 and triggering a Vav1–PLC-γ1 cascade that elevates intracellular Ca²⁺, activates PKC-θ, NFAT, NF-κB and AP-1, and thereby drives γδ T-cell cytotoxicity, cytokine release and tumor lysis.
Picture
Picture
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