LIVE/DEAD™ Fixable Dead Cell Stain Sampler Kit
LIVE/DEAD™ Fixable Dead Cell Stain Sampler Kit
Invitrogen™

LIVE/DEAD™ Fixable Dead Cell Stain Sampler Kit

LIVE/DEAD™ Fixable dead cell stains are used to determine the viability of cells prior to the fixation and permeabilization required자세히 알아보기
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카탈로그 번호수량
L349601 kit
카탈로그 번호 L34960
제품 가격(KRW)
692,000
온라인 행사
Ends: 31-Dec-2025
813,000
할인액 121,000 (15%)
Each
카트에 추가하기
수량:
1 kit
제품 가격(KRW)
692,000
온라인 행사
Ends: 31-Dec-2025
813,000
할인액 121,000 (15%)
Each
카트에 추가하기
LIVE/DEAD™ Fixable dead cell stains are used to determine the viability of cells prior to the fixation and permeabilization required for intracellular antibody staining or prior to elimination of biohazardous materials using formaldehyde fixation. The stains in the sampler kit have been optimized and validated for use in flow cytometry.

• Stable—dyes are freeze-dried in separate vials to maintain stability
• Robust—staining pattern is the same before and after fixation
• Bright signal—allows for easy distinction between live/dead cells in single channel

View a selection guide for all fixable viability dyes for flow cytometry.

Stable
Unlike products that are sold in solution, the LIVE/DEAD™ Fixable dead cell stains in this sampler kit have been conveniently packaged in eight 40-test vials to help ensure the stability and performance of the dye over time. Amine-reactive dyes in solution will lose their effectiveness over a short period of time, therefore it is recommended to use the vial completely once rehydrated or aliquot the solution and store at -80°C, avoiding freeze thaw cycles.

Robust
Dead cell discriminator stains can lose sensitivity after treatment with formaldehyde or ethanol-based fixatives required for intracellular phosphorylation studies. The LIVE/DEAD™ Fixable dead cell stains are amine-reactive dyes that bind covalently to intracellular and extracellular amines, allowing the staining pattern to be preserved following formaldehyde fixation.

Optimal brightness
The LIVE/DEAD™ Fixable dead cell stains were selected based on their fluorescent properties to provide a bright signal when excited with the optimal lasers. Since live and dead cells can be discriminated using a single dye and a single channel of a flow cytometer, these dead cell stains are an ideal choice for multi-color experiments.

How it works
In cells with compromised membranes, the dead cell stain reacts with free amines both in the cell interior and on the cell surface, yielding intense fluorescent staining. In viable cells, the dye's reactivity is restricted to the cell-surface amines, resulting in less intense fluorescence. The difference in intensity is typically greater than 50-fold between live and dead cells allowing for easy discrimination.

Colors available
LIVE/DEAD™ Fixable dead cell stains are available in a wide variety of colors to meet your multi-color panel needs. The sampler kit provides one vial (40 assays) of each of the eight dead cell stains available.

Find the LIVE/DEAD™ Fixable Dead Cell Stain that fits your needs:

• For UV lasers: blue
• For violet lasers: aqua, violet, or yellow
• For blue lasers: green or red
• For red lasers: far-red or near-IR
For Research Use Only. Not for use in diagnostic procedures.
사양
세포 투과성Impermeant
세포 유형Eukaryotic Cells
설명LIVE/DEAD™ Fixable Dead Cell Stain Sampler Kit
검출 방법Fluorescence
염료 유형Other Label(s) or Dye(s)
형태Solid
형식Tube(s)
수량1 kit
배송 조건Room Temperature
용해도DMSO (Dimethylsulfoxide)
색상Various
Emission450/451/526/575/520/615/665/775
Excitation Wavelength Range350/416/367/400/495/595/650/750 nm
용도(애플리케이션)Viability Assay
용도 (장비)Flow Cytometer
제품라인LIVE/DEAD, Molecular Probes
제품 유형Dead Cell Stain Sampler Kit
Unit SizeEach
구성 및 보관
Contians 8 vials (1 vial per color) of the LIVE/DEAD™ fixable dead cell stains and 500 μL DMSO.

Store at -20°C.

자주 묻는 질문(FAQ)

I need to use a dead cell control for my viability assay. Do you have a protocol for killing cells for this?

Heat killing is commonly used. Place your cells in a tube in buffer and heat at 60oC for 20 minutes. You can also kill your cells by fixing them with ice cold 70% ethanol for 15 minutes. The ethanol-killed cells can then be stored at -20oC until needed, at which point you wash out the ethanol and replace with buffer.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

Regarding the LIVE/DEAD Fixable Dead Cell Stain Kits, which can discriminate between live and dead cells using flow cytometry with one emission wavelength. Can these kits be used with microscopy?

This dye gives a dim surface label for live cells, but is internalized and gives a brighter signal for dead cells. Flow cytometry is a very sensitive technique and can easily distinguish between the two populations. Microscopy is not as sensitive and may not be able to distinguish the cells because of a less sensitive detector.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.