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Anti digoxigenin rhodamine red

Manufactured by Roche
Sourced in United States

Anti-digoxigenin-rhodamine (red) is a fluorescent probe used in various laboratory techniques. It binds to digoxigenin, a hapten commonly used for labeling and detection in molecular biology applications. The rhodamine dye attached to the anti-digoxigenin provides a red fluorescent signal that can be detected and visualized.

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4 protocols using anti digoxigenin rhodamine red

1

Dual-Color Fluorescence In Situ Hybridization for Metaphase Chromosomes

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Dual-color FISH (fluorescence in situ hybridization) and the detection of metaphase chromosome specimens were performed according to a previous [36 (link)]. The second round of LA-PCR products labeled with DIG (Digoxigenin-11-dUTP, Roche) and specific Biotin (Biotin-16-dUTP) labeled bacterial artificial chromosome (BAC) clones (52D06) were used as probes, which were detected by Anti-Digoxigenin-Rhodamine (red) and FITC-Anti-Biotin (green) (Roche Diagnostics, USA), respectively. Cot-1 DNA was used to pre-hybridize for blocking the repetitive sequences. Chromosomes were counterstained by 4′, 6-diamidino-2-phenylindole (DAPI) in VECTASHIELD anti-fade solution (Vector Laboratories, Burlingame, CA). The hybridization signals were observed using a fluorescence microscope with a change-coupled device (CCD) camera (Zeiss Axiokop2 plus). The images were adjusted using Adobe Photoshop CS3 software.
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2

Chromosome Preparation and FISH Procedure

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Chromosome Preparation and the FISH procedure were conducted according to the previous protocols [45 (link), 46 ]. The probes were detected with anti-digoxigenin-rhodamine (red) (Roche, USA). Images were captured using a CCD camera attached to a Zeiss Imager M1 microscope. Images were processed using Photoshop CS3.
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3

Mitotic Chromosome FISH Protocol

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Mitotic chromosome preparation and FISH procedures were conducted using a modified protocol (Wang et al. 2001b ). Biotin-labeled and digoxigenin-labeled probes were detected by avidin-fluorescein (green) and anti-digoxigenin-rhodamine (red) (Roche Diagnostics, USA), respectively. Chromosomes were counterstained by

4’,6-diamidino-2-phenylindole

(DAPI)
in antifade VECTASHIELD solutions (Vector Laboratories, Burlingame, CA). The concentration of block DNA (genomic DNA) was 200 times that of the chromosome-specific BAC DNA. The hybridization signals were observed using a fluorescence microscope (Leica MRA2) with a

charge-coupled device

(CCD)
camera. Final image adjustments were performed using Adobe Photoshop CS3 software.
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4

Mitotic Chromosome FISH Assay

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Mitotic chromosomes preparation and FISH procedure were conducted using a modified protocol [61 ]. Biotin-labeled and digoxigenin-labeled probes were detected by avidin-fluorescein (green) and anti-digoxigenin-rhodamine (red) (Roche Diagnostics, USA), respectively. Chromosomes were counterstained by 4′,6-diamidino-2-phenylindole (DAPI) in the antifade VECTASHIELD solutions (Vector Laboratories, Burlingame, CA). For the probe-cocktail mixture, gDNA was used as block DNA. The dose of block DNA was 200 times of the chromosome-specific BAC DNA. The hybridization signals were observed using a fluorescence microscope (Leica MRA2) with a charge-coupled device (CCD) camera (Zeiss Axioskop2 plus). Final image adjustments were performed by using Adobe Photoshop CS3 software.
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