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Donkey anti rabbit tritc

Manufactured by Thermo Fisher Scientific
Sourced in United States

Donkey-anti-rabbit TRITC is a secondary antibody conjugated with the fluorescent dye TRITC (Tetramethylrhodamine). It is designed to detect and bind to primary antibodies raised in rabbit. This product can be used in various immunodetection techniques, such as immunofluorescence, flow cytometry, and Western blotting, to visualize and locate rabbit-derived target proteins or antigens.

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2 protocols using donkey anti rabbit tritc

1

Cloning and Immunofluorescence of Dynactin-1

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The carboxyterminal part of dynactin-1-p150Glued was RT-PCR-cloned from human glioblastoma cDNA using primers attB1-dyn 2532 (5′-AAA AAG CAG GCT TCA CCA TGG CAG CTG CTG CTG CC-3′, sense) and attB2-dyn 3837 (AGA AAG CTG GGT GTT AGG AGA TGA GGC GAC TGT G-3′, antisense). AttB1 and attB2 sites were extended in a second PCR and products were cloned via pDONR201 in p3xflg-CMV (Invitrogen, Carlsbad, CA, USA) to generate p3xflg-CMV-dyn 2532–3837. Plasmids were transfected into COS1 cells in 8-well glass slides (Lab-Tek Chamber Slide™ System, Nunc, Roskilde, Denmark). Forty-eight hours later, cells were fixed with ice-cold acetone and incubated with nanobody C-C7 for 1 hr, followed by sequential incubations with mouse anti-VSV and goat-anti-mouse FITC (Invitrogen, Carlsbad, CA, USA). After washing, slides were stained with rabbit-anti-dynactin-1 which was detected with donkey-anti-rabbit TRITC (Invitrogen, Carlsbad, CA, USA). Images were processed on a Leica Discovery Fluorescence Microscope and a Leica confocal microscope.
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2

Cardiac Microtissue Immunostaining Protocol

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At the final time point of six days, cardiac microtissues were fixed in 4% paraformaldehyde. Immunostaining was performed as described previously [5 (link)] using the following antibodies: mouse anti-cardiac troponin T (cTNT) (Abcam; 1:100), mouse anti-α-actinin (Abcam, 1:20), rabbit anti-connexin 43 (Cx43) (Abcam, 1:500), goat anti-mouse-Alexa Fluor 488 (Jackson ImmunoResearch; 1:400) and donkey anti-rabbit-TRITC (Invitrogen; 1:400). Phalloidin (Invitrogen 1:100) was used to detect actin fibers. Cells were visualized using a fluorescence confocal microscope (Zeiss LSM-510).
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