| Field | Specification |
|---|---|
| Mfr No | |
| Clonality | |
| Conjugate | |
| Host | |
| Immunogen | Human peripheral blood T lymphocytes |
| Isotype | |
| Product Type | |
| Reactivity | |
| Storage | |
| Target |
Overview
CD16 PE is a Mouse monoclonal targeting CD16, supplied as a PE format for FC workflows. It supports measurement of Baboon, Cynomolgus monkey, Human, Rhesus target expression in common experimental systems.
Key elements and design rationale
- Clone: 3G8 — consistent clone identity can support panel reproducibility and cross-study comparisons.
- Isotype: IgG1, k — informs selection of matched controls and secondary reagents when relevant.
- Conjugate: PE — enables direct detection in fluorescence-based assays. Excitation is typically matched to Blue (488nm) lasers in cytometer configurations.
- Host species: Mouse — useful for panel design and control strategy planning.
- Reactivity: Baboon, Cynomolgus monkey, Human, Rhesus — interpret staining in the context of species-specific sequence and expression differences.
Key specifications such as clone identity, isotype, and fluorophore conjugation help researchers align panel design, control selection, and instrument configuration with the biological question and sample type.
Biological background
CD16 (3G8) binds to the 50-65 kDa transmembrane protein of IgG FcγRIII, an surface antigen commonly associated with human NK cells. Besides surface expression on NK cells, it is also expressed on activated monocytes, macrophages, on neutrophils and placental trophoblasts in humans. CD16 binds aggregated IgG or IgG-antigen complex which functions in NK cell activation, phagocytosis, and antibody-dependent cell-mediated cytotoxicity (ADCC). 3G8 is also useful in experiments related to immunohistochemical staining, immunoprecipitation, NK cell proliferation, blocking of phagocytosis and blocking of immunoglobulin binding tthrough FcγRIII.
Research relevance and current trends
- High-parameter immunophenotyping: combining CD16 with complementary lineage and activation markers to resolve complex cell states.
- Panel standardization and data comparability: increasing emphasis on consistent reagents, compensation-aware fluorophore choices, and shared gating strategies.
- Integration with single-cell multi-omics: pairing surface marker profiling with transcriptomic or proteomic readouts to connect phenotype to function.
Common research applications
- Flow cytometry: quantify CD16-positive populations and compare expression distributions across conditions or time points.
- Cell sorting: enrich CD16-defined subsets for downstream RNA/protein assays or functional readouts.
Changes in measured signal are typically interpreted in the context of cell subset frequency, activation/differentiation state, and sample processing effects rather than as a standalone readout.
Notes for experimental interpretation
- Fluorophore selection: consider brightness, spectral overlap, and instrument configuration; compensation and spillover can affect apparent population boundaries.
- Biology-driven confounders: activation state, differentiation, and isoform/PTM variation can shift epitope accessibility and apparent expression.
- Control concepts: include matched isotype and fluorescence-minus-one (FMO) controls where appropriate, and interpret results alongside biological positive/negative reference samples.
For antibody-based assays, monoclonal versus polyclonal format can influence epitope recognition breadth and signal consistency. Conjugated antibodies support direct detection and can simplify multicolor panel design when paired with appropriate controls and instrument settings.
Customization & Add-ons: Can’t find the antibody you need—or require a custom format for your assay? We can help you source the best match or support custom antibody solutions for diverse research needs, including species and isotype selection, conjugations and labeling (e.g., HRP/AP, biotin, fluorophores), purification grade options (Protein A/G, affinity purified), formulation preferences (buffer selection, carrier-free, glycerol-free), custom concentrations and aliquoting, low-endotoxin options for cell-based work, and application-focused QC/validation support (project dependent). Click Talk to a Scientist to submit a request, email us at support@biohippo.com, or explore our Research Services for additional support—our team will follow up with feasibility details and next steps.
