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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货号数量
S327113 x 1 mL
S327101 mL
货号 S32711
价格(CNY)
3,975.00
飞享价
Ends: 31-Dec-2026
5,445.00
共减 1,470.00 (27%)
Each
数量:
3 x 1 mL
价格(CNY)
3,975.00
飞享价
Ends: 31-Dec-2026
5,445.00
共减 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.
规格
细胞渗透性Live and Fixed Cell Permeable
颜色Red
最大浓度1 mM in 25% DMSO/DI H2O
检测方法Fluorescence with Texas Red Filter Set
染料类型Fluorogenic Organic Dye
发射626 nm
激发波长范围595 nm
适用于(应用)Live Cell Imaging, Fixed Cell Imaging, High Content Screening, Fluorescence Microscopy
适用于(设备)Fluorescence Microscope, Spectral Imaging Instrument, Flow Cytometer, High Content Imager
形式Aqueous Liquid with 25% DMSO
产品规格Vial
测试数量300 Tests
产品线SYTO RNASelect
数量3 x 1 mL
反应性RNA, Nucleolar Structure
试剂类型Fluorogenic RNA Label
靶标RNA
技术High Content Imaging
经证实的应用Live Cell Imaging, Fixed Cell Imaging, High Content Imaging
容积(公制)900 μL
标签类型Fluorescent Dye
产品类型RNA-specific Label
亚细胞定位Nucleolus
Unit SizeEach
内容与储存
•3 Vials
•Store at 2°C to 30°C
•Protect from light
•Do not freeze

常见问题解答 (FAQ)

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.