Flow cytometric analysis of Rat CD3 expression on SD Rat splenocytes. SD Rat splenocytes were stained with either Alexa Fluor® 488 Mouse IgG2b Isotype Control (Black line histogram) or SDT Alexa Fluor® 488 Mouse Anti-Rat CD3 Antibody (Red line histogram) at 5 μl/test, cells without incubation with primary antibody and secondary antibody (Blue line histogram) was used as unlabelled control. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.
Product Details
Product Details
Product Specification
| Host | Mouse |
| Antigen | CD3 |
| Synonyms | T-cell surface glycoprotein CD3 gamma chain; T-cell receptor T3 gamma chain; Cd3g |
| Location | Cell membrane |
| Accession | Q64159、P19377 |
| Clone Number | S-3399 |
| Antibody Type | Mouse mAb |
| Isotype | IgG2b |
| Application | FCM |
| Reactivity | Rt |
| Positive Sample | SD Rat splenocytes |
| Purification | Protein A |
| Concentration | 0.2 mg/ml |
| Conjugation | Alexa Fluor® 488 |
| Physical Appearance | Liquid |
| Storage Buffer | PBS, 1% BSA, 0.3% Proclin 300 |
| Stability & Storage | 12 months from date of receipt / reconstitution, 2 to 8 °C as supplied |
Dilution
| application | dilution | species |
| FCM | 5μl per million cells in 100μl volume | Rt |
Background
CD3 is a multimeric protein complex that serves as a crucial T-cell co-receptor, composed of four distinct chains (CD3γ, δ, ε, ζ) that non-covalently associate with the T-cell receptor (TCR), where its cytoplasmic immunoreceptor tyrosine-based activation motifs (ITAMs) become phosphorylated upon antigen recognition to initiate downstream signaling cascades leading to T-cell activation, differentiation, and effector functions, making it an essential component of adaptive immunity and a valuable target for therapeutic interventions such as the immunosuppressive agent muromonab-CD3 and emerging bispecific antibodies in oncology.
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