SYTO™ RNASelect™ Red
Invitrogen™

SYTO™ RNASelect™ Red

SYTO™ RNASelect™ Red fluorescent cell label offers RNA-selective bright red fluorescence in live or fixed cells, highlighting nucleoli and cytoplasmic RNA while preserving the green channel for multiplex imaging. Ideal for cell stress and deep-learning assays.
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Catalog NumberQuantity
S327113 x 1 mL
S327101 mL
Catalog number S32711
Price (CNY)
3,975.00
飞享价
Ends: 31-Dec-2026
5,445.00
Save 1,470.00 (27%)
Each
Quantity:
3 x 1 mL
Price (CNY)
3,975.00
飞享价
Ends: 31-Dec-2026
5,445.00
Save 1,470.00 (27%)
Each
SYTO™ RNASelect™ Red is a cell-permeant, RNA-selective fluorescent dye for live or fixed eukaryotic cells. It helps visualize RNA-rich nucleoli together with weaker nuclear and cytoplasmic RNA-associated signal in a Texas Red/RFP-compatible channel. Compared with SYTO™ RNASelect™ Green, it supports 4% paraformaldehyde workflows rather than methanol fixation and helps keep GFP/FITC channels open for antibodies, reporters, or other probes in multiplex and high-content imaging.

SYTO™ RNASelect™ is a bright photostable cell-permeant, RNA-selective fluorescent stain for imaging endogenous RNA organization in live or fixed eukaryotic cells. This molecular probe is a ready-to-use 100x aqueous solution to add directly to media or buffer to label cells.

Red-channel detection supports Texas Red filter sets, helping reserve GFP/FITC channels for antibodies, fluorescent proteins, or other structural markers.

Compatibility with 4% paraformaldehyde-based workflows and with downstream permeabilization or immunofluorescence workflows expands applications into high content screening for nucleolar reorganization, cell stress assays, and deep learning computational models.

Staining is with high-affinity with RNA specificity, with additional nuclear and cytoplasmic RNA-associated signal for visualization of RNA-rich cellular compartments.

RNase-responsive staining pattern supports use as an RNA-associated imaging readout, and can be multiplexed with other nucleic acid labels.

Features

  • Suitable for live-to-fixed workflows, connecting live-cell observation with endpoint imaging.
  • Compatible with multiplex imaging when paired with spectrally separated markers such as Hoechst/DAPI, phalloidin, ER, or mitochondrial probes.
  • Applicable to high-content imaging and RNA-focused 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.

Complements SYTO™ RNASelect™ Green in channel planning and fixation choice: SYTO™ RNASelect™ Green remains the better fit when methanol fixation is required, whereas SYTO™ RNASelect™ Red is appropriate when a red RNA channel or 4% PFA workflow is preferred.

Available 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
Quantity3 x 1 mL
ReactivityRNA, Nucleolar Structure
Reagent TypeFluorogenic RNA Label
TargetRNA
TechniqueHigh Content Imaging
Validated ApplicationLive Cell Imaging, Fixed Cell Imaging, High Content Imaging
Volume (Metric)900 μL
Label TypeFluorescent Dye
Product TypeRNA-specific Label
SubCellular LocalizationNucleolus
Unit SizeEach
Contents & Storage
•3 Vials
•Store at 2°C to 30°C
•Protect from light
•Do not freeze

Frequently asked questions (FAQs)

The process of purifying exosomes using ultra-centrifugation differs greatly among published papers. How can I determine which protocol is most suitable for my cell line?

There are some variations to the ultracentrifugation protocols, not based on the cell lines used so much as the experience in that particular lab, including what G-force they recommend, duration of ultra-centrifugation, straight sedimentation vs cushion vs sucrose gradients to obtain the top quality exosomes at reasonable yields. We often recommend protocols developed by Clothilde: C. Thery, S. Amigorena, G. Raposo and A. Clayton “Isolation and characterization of exosomes from cell culture supernatants and biological fluids.” Curr. Protoc. Cell. Biol., Chapter 3, Unit 3: 22, 2006.