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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카탈로그 번호수량
S327113 x 300 μL
S32710300 μL
카탈로그 번호 S32711
제품 가격(KRW)
-
수량:
3 x 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.
사양
세포 투과성Live and Fixed Cell Permeable
색상Red
농도1 mM in 25% DMSO/DI H2O
검출 방법Fluorescence with Texas Red Filter Set
염료 유형Fluorogenic Organic Dye
방출626 nm
여기 파장 범위595 nm
용도(애플리케이션)Live Cell Imaging, Fixed Cell Imaging, High Content Screening, Fluorescence Microscopy
용도(장비)Fluorescence Microscope, Spectral Imaging Instrument, Flow Cytometer, High Content Imager
형태Aqueous Liquid with 25% DMSO
형식Vial
테스트 수900 Tests
제품라인SYTO RNASelect
수량3 x 300 μL
반응성RNA, Nucleolar Structure
시약 유형Fluorogenic RNA Label
타겟RNA
기술High Content Imaging, Fluorescence Microscopy
검증된 애플리케이션Live Cell Imaging, Fixed Cell Imaging, High Content Imaging
부피(미터법)900 μL
라벨 유형Fluorescent Dye
제품 유형RNA-specific Label
Sub Cellular LocalizationNucleolus
Unit SizeEach
구성 및 보관
•3 Vials
•Store at 2°C to 30°C
•Protect from light
•Do not freeze

자주 묻는 질문(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.