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Dylight 594 labeled anti digoxigenin antibody

Manufactured by Vector Laboratories
Sourced in Switzerland

The DyLight 594 Labeled Anti-Digoxigenin antibody is a detection reagent used in various biotechnological and immunological applications. It is a conjugate of an anti-digoxigenin antibody and the fluorescent dye DyLight 594. The primary function of this product is to enable the visualization and detection of digoxigenin-labeled targets in samples.

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2 protocols using dylight 594 labeled anti digoxigenin antibody

1

Telomere FISH Probing in Monosiga

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Unlabeled telomeric probes were generated using the primer dimer extension method described in Ijdo et al. (1991 (link)), but we used PrimeSTAR Max DNA polymerase (Clontech, R045A) instead of Taq polymerase for the PCR step. The purified PCR products were labeled with digoxigenin-11-dUTP, alkali stabile (Roche, 11093088910) using the DecaLabel DNA Labeling Kit (Thermo Scientific, K0621). The labeled probes were purified using columns from the QIAquick Gel Extraction Kit (Qiagen, 28704) and eluted into the final volume of 50 µl.
One liter of M. exilis culture was filtered to remove bacteria and the cells were pelleted by centrifugation for 10 min at 1,200 × g at 4 °C. FISH with digoxigenin-labeled probes was performed according to the previously described procedure (Zubáčová et al. 2011 (link)) except that the culture was not treated with colchicine and the stringency washes were performed at 45 °C. For probe detection, we used DyLight 594 Labeled Anti-Digoxigenin antibody (Vector Laboratories, DI-7594). Preparations were observed using an IX81 microscope (Olympus) equipped with an IX2-UCB camera. Images were processed using Cell-R software (Olympus) and Image J 1.42q. The number of signals from each nucleus was manually counted and the average number of signals was estimated from at least 50 nuclei.
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2

EBER-FISH Assay for EBV Detection

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To validate and confirm infection of AGS cells, EBER-FISH was performed using DIG-labeled probes specific for EBERs (PanPath, Budel, Netherlands). Hybridization was performed according to the manufacturer’s instructions. Briefly, inoculated cells were seeded on microscopy chamber slides (BD Falcon CultureSlides, BD Bioscience). At the indicated time points cells were fixed with 4% Roti-Histofix (Carl Roth AG, Arlesheim, Switzerland) for 15 min at room temperature (RT), washed with 1x PBS, rinsed with ddH2O and dehydrated in 100% EtOH. Subsequently, cells were hybridized with the EBER-probes for 2 h at 37°C in a moist environment. Slides were then washed with 1x PBS and incubated with the secondary Dylight594-labeled anti-Digoxigenin antibody (Vector Laboratories, RECATOLAB, S.A., Servion, Switzerland) for 30 min at RT, washed again with 1x PBS and rinsed with ddH2O. After removing most of the remaining liquid, slides were mounted with VECTASHIELD Mounting Medium (Vector Laboratories) containing 4’,6-diamidino-2-phenylindole (DAPI) to counterstain the nucleus. Slides were analyzed using a fluorescence microscope Axioskop 2 MOT plus (Carl Zeiss, Jena, Germany) and images were process with the AxioVision Rel. 4.8.2 software (Carl Zeiss).
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