{"product_id":"cd16-ifluor700-bha19900989","title":"CD16 iFluor700","description":"\u003ch2\u003eOverview\u003c\/h2\u003e\u003cp\u003eCD16 iFluor700 is a Mouse monoclonal targeting CD16, supplied as a iFluor™ 700 format for FC workflows. It supports measurement of Baboon, Cynomolgus monkey, Human, Rhesus target expression in common experimental systems.\u003c\/p\u003e\u003ch2\u003eKey elements and design rationale\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003e\n\u003cstrong\u003eClone:\u003c\/strong\u003e 3G8 — consistent clone identity can support panel reproducibility and cross-study comparisons.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eIsotype:\u003c\/strong\u003e IgG1, k — informs selection of matched controls and secondary reagents when relevant.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eConjugate:\u003c\/strong\u003e iFluor™ 700 — enables direct detection in fluorescence-based assays. Excitation is typically matched to Red (633nm) lasers in cytometer configurations.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eHost species:\u003c\/strong\u003e Mouse — useful for panel design and control strategy planning.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eReactivity:\u003c\/strong\u003e Baboon, Cynomolgus monkey, Human, Rhesus — interpret staining in the context of species-specific sequence and expression differences.\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKey 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.\u003c\/p\u003e\u003ch2\u003eBiological background\u003c\/h2\u003e\u003cp\u003eCD16 (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.\u003c\/p\u003e\u003ch2\u003eResearch relevance and current trends\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003eHigh-parameter immunophenotyping: combining CD16 with complementary lineage and activation markers to resolve complex cell states.\u003c\/li\u003e\n\u003cli\u003ePanel standardization and data comparability: increasing emphasis on consistent reagents, compensation-aware fluorophore choices, and shared gating strategies.\u003c\/li\u003e\n\u003cli\u003eIntegration with single-cell multi-omics: pairing surface marker profiling with transcriptomic or proteomic readouts to connect phenotype to function.\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eCommon research applications\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003eFlow cytometry: quantify CD16-positive populations and compare expression distributions across conditions or time points.\u003c\/li\u003e\n\u003cli\u003eCell sorting: enrich CD16-defined subsets for downstream RNA\/protein assays or functional readouts.\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eChanges 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.\u003c\/p\u003e\u003ch2\u003eNotes for experimental interpretation\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003eFluorophore selection: consider brightness, spectral overlap, and instrument configuration; compensation and spillover can affect apparent population boundaries.\u003c\/li\u003e\n\u003cli\u003eBiology-driven confounders: activation state, differentiation, and isoform\/PTM variation can shift epitope accessibility and apparent expression.\u003c\/li\u003e\n\u003cli\u003eControl concepts: include matched isotype and fluorescence-minus-one (FMO) controls where appropriate, and interpret results alongside biological positive\/negative reference samples.\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eFor 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.\u003c\/p\u003e\u003c!-- Sources (internal): - UniProt Knowledgebase — UniProt — https:\/\/www.uniprot.org\/ - NCBI Gene — NCBI — https:\/\/www.ncbi.nlm.nih.gov\/gene\/ - HGNC gene nomenclature — HUGO Gene Nomenclature Committee — https:\/\/www.genenames.org\/ - Flow cytometry basics — NIH\/NCI (overview resources) — https:\/\/www.cancer.gov\/research\/resources - High-dimensional cytometry overview — Nature Methods (journal) — https:\/\/www.nature.com\/nmeth\/ --\u003e","brand":"Caprico","offers":[{"title":"50 Tests","offer_id":53072783016301,"sku":"4014192","price":295.0,"currency_code":"USD","in_stock":true},{"title":"100 Tests","offer_id":53072861725037,"sku":"4014195","price":475.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0949\/7424\/7277\/files\/20180731-CD16-iFluor700-3G8-14A6F1-1_0be0d2bb-1157-4bbf-8e98-7317023ac6f3.jpg?v=1772634936","url":"https:\/\/www.ebiohippo.com\/products\/cd16-ifluor700-bha19900989","provider":"BioHippo","version":"1.0","type":"link"}