Not exact matches
Typically, detection of biomolecules such as proteins are performed
using colorimetric assays or fluorescent
labelling with a
secondary antibody for detection, and requires complex optical detection equipment such as fluorescent microscopy or spectrophotometry.
Immunoreactions were developed
using a fluorescently
labeled secondary antibody, and samples visualized in a Leica Biosystems epifluorescent microscope or
using a
secondary antibody linked to horseradish peroxidase and developed with a 3,3 ′ - diaminobenzidine kit.
Immunofluorescent
labeling was performed
using anti-Olig2 (1 ∶ 4000, Chemicon) and anti-GFAP (1 ∶ 400, Cell Signaling) followed by fluorescently
labeled,
secondary anti-Ig
antibodies (Alexa 488 and 568 conjugates, Invitrogen) at a 1 ∶ 2000 dilution.
Antibody binding was visualized by chemiluminescence detection in a CCD - camera system using a peroxidase (HRP) labeled secondary a
Antibody binding was visualized by chemiluminescence detection in a CCD - camera system
using a peroxidase (HRP)
labeled secondary antibodyantibody.
Secondary labeling was carried out using isotype matched Alexa - fluor labeled secondary antibodies (AF488, 568 and 594, all from Invitrog
Secondary labeling was carried out
using isotype matched Alexa - fluor
labeled secondary antibodies (AF488, 568 and 594, all from Invitrog
secondary antibodies (AF488, 568 and 594, all from Invitrogen Corp).
Appropriately coupled
secondary antibodies (Molecular Probes) were
used for single and double
labeling.