SYTO™ RNASelect™ Red
Invitrogen™

SYTO™ RNASelect™ Red

SYTO™ RNASelect™ Red is a cell-permeant, RNA-selective fluorescent dye for live or fixed eukaryotic cells. It allows researchers to visualize RNA-rich nucleoli and cytoplasmic RNA in a Texas Red/RFP compatible channel.
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Catalog NumberQuantity
S32710300 μL
S327113 x 300 μL
Catalog number S32710
Price (MXN)
-
Quantity:
300 μL

SYTO™ RNASelect™ Red is a cell-permeant, RNA-selective fluorescent dye for live or fixed eukaryotic cells. It allows researchers to visualize RNA-rich nucleoli and cytoplasmic RNA in a Texas Red/RFP compatible channel. Compared to SYTO™ RNASelect™ Green, it is compatible with 4% paraformaldehyde fixation rather than methanol fixation, and leaves GFP/FITC channels open for antibodies, fluorescent proteins, and other fluorescent probes in multiplex and high-content imaging.

This molecular probe is prepared as a ready-to-use 100x aqueous solution, appropriate for direct addition to either complete media or other buffers of your choice to then be used in staining cells.

Compatibility with 4% paraformaldehyde fixation and permeabilization expands the applicability of this RNA dye for immunofluorescence workflows, enabling its use in high content screening for nucleolar reorganization, cell stress assays, and deep learning computational models.

The staining patterns demonstrate high RNA specificity, with expected staining demonstrating bright nucleoli and diffuse ribosomal staining throughout the cytoplasm and is easily multiplexable with classic nuclear stains such as Hoechst 33342 or DAPI. This specificity is demonstrated by the sharp decrease in staining intensity upon treatment with RNase, all red signal is quickly depleted while the nuclear DNA dye staining remains intact.

Features

  • Suitable for both live and fixed cell workflows, connecting live cell observation with endpoint imaging.
  • Compatible with multiplex imaging outside of the Texas Red/RFP channels with various organelle markers such as Hoechst/DAPI, phalloidin, ER, lectins, or mitochondrial probes.
  • Applicable to high-content imaging and RNA based nucleolar morphology studies, including workflows where nucleolar signal is used for segmentation or comparative phenotyping.

For researchers familiar with SYTO™ 14, SYTO™ RNASelect™ Red offers a red channel option for RNA associated morphology in Cell Painting related or other multiplex imaging workflows.

This dye complements SYTO™ RNASelect™ Green in channel planning and fixation choice: SYTO™ RNASelect™ Green remains the better fit when the green channel is desired and the sample type requires methanol fixation, whereas SYTO™ RNASelect™ Red is appropriate when a red RNA channel or 4% PFA workflow is preferred.

Available as a single vial as S32710 and in a 3-pack format as S32711.

For Research Use Only.
Specifications
Cell PermeabilityLive and Fixed Cell Permeable
ColorRed
Concentration1 mM in 25% DMSO/DI H2O
Detection MethodFluorescence with Texas Red Filter Set
Dye TypeFluorogenic Organic Dye
Emission626 nm
Excitation Wavelength Range595 nm
For Use With (Application)Live Cell Imaging, Fixed Cell Imaging, High Content Screening, Fluorescence Microscopy
For Use With (Equipment)Fluorescence Microscope, Spectral Imaging Instrument, Flow Cytometer, High Content Imager
FormAqueous Liquid with 25% DMSO
FormatVial
No. of Tests300 Tests
Product LineSYTO RNASelect
Quantity300 μL
ReactivityRNA, Nucleolar Structure
Reagent TypeFluorogenic RNA Label
TargetRNA
TechniqueHigh Content Imaging, Fluorescence Microscopy
Validated ApplicationLive Cell Imaging, Fixed Cell Imaging, High Content Imaging
Volume (Metric)300 μL
Label TypeFluorescent Dye
Product TypeRNA-specific Label
Sub Cellular LocalizationNucleolus
Unit SizeEach
Contents & Storage
•1 Vial
•Store at 2°C to 30°C
•Protect from light
•Do not freeze

Frequently asked questions (FAQs)

How can I prepare my exosome sample (isolated using the Total Exosome Isolation reagent) for analysis by mass spectroscopy?

The Total Exosome Isolation reagent allows recovery of the entire exosome population from the sample, in contrast to ultracentrifugation protocols, which recover significantly less material. Thus, the pellet is larger. The purity of exosomes is very similar for cell media samples (reagent vs ultra); for more challenging samples such as serum (which are more viscous and have much higher protein content, etc.) the reagent recovers exosomes at a lower purity (few microvesicles and large protein complexes co-precipitate) compared to ultracentrifugation. Having said this, you can obtain enough material for all standard types of downstream analysis, such as qRT-PCR or Western blot with either method.