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An electrochemical ELISA-like amplification strategy was set up using a secondary antibody conjugated to horseradish peroxidase (HRP).
Monoclonal antibody BM1234 was added to acetone/methanol-fixed P. falciparum cultures of the 3D7 strain, and its binding was detected by confocal fluorescence microscopy using a secondary antibody (green).
We have designed and optimized a classical ELISA in which Epi-hNE4 was coated directly on microtitre plates and the antibodies were detected using a secondary antibody labelled with peroxidase.
Bound antibodies are visualized using a secondary antibody conjugated to colloidal gold particles.
Antibody binding was visualised using a secondary antibody (polyclonal, Cy5TM-conjugated anti-mouse IgG from goat; Zymed).
After overnight coating of a 96-well plate with a primary antibody, TGF-β1 was detected in cell lysates using a secondary antibody.
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EnVision uses a secondary antibody against both rabbit and mouse that is directly labelled with HRP (horseradish peroxidase) reacting with DAB, whereas LSAB uses a secondary antibody against rabbit and mouse, labelled with biotin, then streptavidin-HRP is added and the staining is done with DAB.
After washing, Envision + polymer (ready to use; Dako) was used as a secondary antibody.
Primary antibodies were detected using a secondary HRP-conjugated antibody.
DakoEnVision™ + HRP-conjugated anti-mouse antibody was used as a secondary antibody, and no counterstain was employed.
was used as a secondary antibody.
More suggestions(15)
using a secondary Rabbit
using a secondary rabbit
using a primary antibody
using a radiolabelled antibody
using a secondary flash
using a secondary class
using a secondary plasma
using a secondary wastewater
using a secondary device
using a secondary electrode
using a secondary structure
using a secondary beam
using a monoclonal antibody
using a polyclonal antibody
using a secondary processor
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