Sentence examples for beads were detected using from inspiring English sources
Specific proteins bound to fluorescent beads were detected using a mix of protein-specific, biotinylated detector antibodies followed by incubation with streptavidin PE.
Fluorescence from the beads was detected using a BD Accury C6 flow cytometer system (Becton Dickinson, San Jose, CA, USA) and analyzed with FCAP Array Software.
After extensive washing, protein DNA binding on beads was detected using anti-DIG antibody conjugated to alkaline phosphatase, which was then measured by a chemiluminescent reaction using a luminometer.
Briefly, magnetic beads were coupled with the c-KIT monoclonal antibody (R&D Systems, Minneapolis, MN, USA; catalogue numbers MAB332) using the BioPlex amine coupling kit (Bio-Rad Laboratories), and c-KIT captured on the beads was detected using the c-KIT polyclonal antibody (R&D Systems; catalogue numbers BAF332).
Bead-pair angles were detected using back focal plane interferometry with a resolution of up to 1°, and controlled using a feedback algorithm with a precision of up to 2° and a bandwidth of up to 1.6 kHz.
Cytokine levels in sera and supernatants were detected using fluorescent beads coated with analyte-specific capture antibodies (BioSource, USA) according to the manufacturer's protocols.
Culture supernatants were collected after 48 hr of co-culture and cytokines in the supernatant were detected using Cytometric Bead Array or by ELISA.
These SNPs were detected using the Illumina Bead Station 500G system.
The beads were used to perform GTPase reaction and were detected using the GTPase-Glo system.
