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DURAClone IF Monocyte Activation

Monocyte activation leads to the differentiation of monocytes to macrophages or myeloid dendritic cells and an increase in their ability to phagocytose, present antigen and release pro-inflammatory cytokines. The DURAClone IF Monocyte panel assesses the inflammatory monocyte response indicating innate immune competence. It utilizes dry reagent technology that confers workflow improvements.

Panel of 4 markers in fluorochrome combinations that provide robust population identification, including CD14, CD45, HLA-DR, TNF alpha
Pre-formulated antibody panel in a unitized assay eliminating antibody cocktailing
25 tests per kit including 3 compensation kits with lot matched tandem dyes

For Research Use Only. Not for use in diagnostic procedures.

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Features Explore DURAClone IF Monocyte Activation Models Content and Resources Technical Documents Related Products

Features

Expert Panels

Proven marker combination to assess monocyte immune competency
Open channels to add drop-in markers to modify for different research questions
Designed for assay precision and lot-to-lot consistency

Efficiency

Eliminate time spent in titrating different antibody lots
Avoid waste that comes from preparing cocktail master mix
Simplify inventory management

Consistency

Unitized assays eliminate error prone pipetting steps
Includes lot matched tandem dyes for compensation controls for improved accuracy
Dry format maintains reagent performance better than liquid under stress conditions

Easy to Use

Ready to use assay with verified panel design
Includes sample preparation and staining procedure
Streamlined workflow, simultaneously stain cell surface and intracellular targets

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NOT ALL PRODUCTS ARE AVAILABLE IN ALL COUNTRIES. PRODUCT AVAILABILITY AND REGULATORY STATUS DEPENDS ON COUNTRY REGISTRATION PER APPLICABLE REGULATIONS The listed regulatory status for products correspond to one of the below: IVD: In Vitro Diagnostic Products. These products are labeled "For In Vitro Diagnostic Use." ASR: Analyte Specific Reagents. These reagents are labeled "Analyte Specific Reagent. Analytical and performance characteristics are not established." CE-IVD, CE: Products intended for in vitro diagnostic use and conforming to the In Vitro Diagnostic Regulation (IVDR) (EU) 2017/746. (Note: Devices may be CE marked to other directives.) RUO: Research Use Only. These products are labeled "For Research Use Only. Not for use in diagnostic procedures." LUO: Laboratory Use Only. These products are labeled "For Laboratory Use Only." No Regulatory Status: Non-Medical Device or non-regulated articles. Not for use in diagnostic or therapeutic procedures.