Not exact matches
Generic
labeling of proteins is achieved through
fluorescent -
antibody binding.
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.
In the Nature Biotechnology study, the researchers used it to anchor proteins, and they also showed that the technique works on tissue that has been previously
labeled with either
fluorescent antibodies or proteins such as green
fluorescent protein (GFP).
Wellington and her colleagues detected the dormant cells with
fluorescent -
labelled antibodies which cling specifically to S. typhimurium.
Furthermore, once these proteins are identified, they can be selectively
labeled with
antibodies linked to green
fluorescent protein (GFP) and directly observed in a cell.
Control and gesicle - treated hiPS cells were assessed for AcGFP1 expression (green),
labeled with an
antibody specific to pluripotency marker Oct ‑ 4, visualized with a
fluorescent -
labeled secondary
antibody (red), and nuclear -
labeled with DAPI (blue).
Many popular methods, such as
antibody labeling, are used to add physical
fluorescent labels to specific cellular constituents.
Generation, purification, and testing of primary
antibodies Gold -, enzyme - and
fluorescent labeling of secondary
antibodies In situ hybridization Light - and electron microscopy
PromoKine offers a wide range of well proven products for cell biology research such as kits and reagents for cell analysis, apoptosis research, cell transfection,
fluorescent labeling, gene cloning & expression, mycoplasma detection and elimination as well as numerous
antibodies, ELISAs, cytokines and growth factors.
For colocalization of both tracers or one tracer together with ZENK signals, primary
antibodies (Egr - 1 / ZENK, 1 ∶ 500; CtB, 1 ∶ 300 in PBS - T) were detected by an appropriate secondary
antibody (polyclonal goat raised against rabbit IgG
labeled with
fluorescent dyes Alexa488; Molecular Probes Europe BV, Leiden, The Netherlands, 1 ∶ 400 in PBS - T).
Such an optical contrast exceeded the optical contrast of the
fluorescent labels (that were targeted to C4 - 2B and HS - 5 cells using the same prostate cancer - specific PSMA
antibody, see Figure 7B, D) by 31 times.