A variety of accessories and solutions to support flow cytometry procedures. Products may include buffer solutions and kits as well as instrument accessories to augment capacity.
Intended to fix and permeabilize cells to enable the staining of intracellular targets with minimal effect on the prior staining of cell surface antigens.
Fluorescent beads that enable the software to determine spillover values (SOVs) for fluorescence compensation and calculate a fluorescence compensation matrix during setup of BD™ flow cytometers.
Fluorescent beads that enable the software to determine spillover values (SOVs) for fluorescence compensation and calculate a fluorescence compensation matrix during setup of BD™ flow cytometers.
Fluorescent beads that enable the software to determine spillover values (SOVs) for fluorescence compensation and calculate a fluorescence compensation matrix during setup of BD™ flow cytometers.
Fluorescent beads that enable the software to determine spillover values (SOVs) for fluorescence compensation and calculate a fluorescence compensation matrix during setup of BD™ flow cytometers.
Fluorescent beads that enable the software to determine spillover values (SOVs) for fluorescence compensation and calculate a fluorescence compensation matrix during setup of BD™ flow cytometers.
Fluorescent beads that enable the software to determine spillover values (SOVs) for fluorescence compensation and calculate a fluorescence compensation matrix during setup of BD™ flow cytometers.
Fluorescent beads that enable the software to determine spillover values (SOVs) for fluorescence compensation and calculate a fluorescence compensation matrix during setup of BD™ flow cytometers.
Fluorescent beads that enable the software to determine spillover values (SOVs) for fluorescence compensation and calculate a fluorescence compensation matrix during setup of BD™ flow cytometers.
Fluorescent beads that enable the software to determine spillover values (SOVs) for fluorescence compensation and calculate a fluorescence compensation matrix during setup of BD™ flow cytometers.