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Rhodamine red

Manufactured by Zeiss
Sourced in Germany

Rhodamine red is a fluorescent dye commonly used in various laboratory applications. It is characterized by its bright red-orange emission spectrum when excited by appropriate light sources. The dye is known for its high quantum yield and photostability, making it a valuable tool for fluorescence-based techniques and imaging.

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2 protocols using rhodamine red

1

Visualizing Coronary Arteriole Proteins

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Coronary arterioles were embedded in OCT compound (Tissue-Tek; Electron Microscopy Sciences, Hatfield, PA, USA) and frozen sections (10 μm thickness) were fixed in 4% paraformaldehyde for immunohistochemical analysis as described previously [83 (link),84 (link)]. Immunolabelling was performed using a mouse monoclonal antibody against eNOS (610297, 1:100 dilution; BD Biosciences, Franklin Lakes, NJ, USA) and a rabbit polyclonal antibody against PKCβ2 (sc-210, 1:100 dilution; Santa Cruz Biotechnology, Dallas, TX, USA). The slides were then incubated with rhodamine red-labeled (Jackson Laboratories, West Grove, PA, USA) and FITC-labeled (Jackson Laboratories) secondary antibodies. Staining control tissues were exposed for the same duration to non-immune serum (Jackson Laboratories) in place of primary antibody. Slides were observed for red (rhodamine red for PKCβ2) and green (FITC for eNOS) images under a fluorescence microscope (Axiovert 200, Zeiss, Jena, Germany) and analyzed using ImageJ software (National Institutes of Health, Bethesda, MD, USA) as described previously [20 (link)].
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2

Localization of Vascular ETA Receptors

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To identify and localize vascular ETA receptors, coronary arterioles were embedded and frozen in OCT compound (Tissue-Tek) [41 (link)]. Frozen sections (10-μm thick) were fixed in 4% paraformaldehyde, and then immunolabeled with specific primary antibodies for ETA receptors (Sigma) and endothelial NOS (eNOS; Santa Cruz Biotechnology). Afterwards, the slides were incubated with rhodamine red-labeled (Jackson Laboratories) and FITC-labeled (Jackson Laboratories) secondary antibodies. Staining control tissues were exposed for the same duration to non-immune serum (Jackson Laboratories) in place of primary antibody. Slides were observed for red (rhodamine red for eNOS) and green (FITC for ETA) images, and analyzed using a fluorescence microscope (Axiovert 200, Zeiss). Merged images were created with ImageJ software.
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