CellTrace™ Far Red Cell Proliferation Kit, for flow cytometry
CellTrace™ Far Red Cell Proliferation Kit, for flow cytometry
Invitrogen™

CellTrace™ Far Red Cell Proliferation Kit, for flow cytometry

CellTrace™ Far Red Cell Proliferation Kit is used for in vitro and in vivo labeling of cells to trace multiple자세히 알아보기
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카탈로그 번호수량
C3457220 Assays
C34564180 Assays
카탈로그 번호 C34572
제품 가격(KRW)
182,000
온라인 행사
Ends: 31-Dec-2025
214,000
할인액 32,000 (15%)
Each
카트에 추가하기
수량:
20 Assays
제품 가격(KRW)
182,000
온라인 행사
Ends: 31-Dec-2025
214,000
할인액 32,000 (15%)
Each
카트에 추가하기
CellTrace™ Far Red Cell Proliferation Kit is used for in vitro and in vivo labeling of cells to trace multiple generations using dye dilution by flow cytometry.

• Superior performance—bright, single-peak staining enables visualization of multiple generations
• Long-term signal stability—well-retained in cells for several days post stain
• Versatile—multiple colors available to easily combine with antibodies or markers of cell function, such as GFP
• Simple, robust staining protocol

View a selection guide for all CellTrace™ Cell Proliferation Kits for flow cytometry.

Superior fluorescent staining
Successful proliferation analysis by dye dilution requires an extremely bright dye to distinguish fluorescently labeled cells from auto-fluorescence after several cell divisions. The intense fluorescent staining provided by CellTrace™ Far Red dye enables the visualization of six or more generations of proliferating cells before the signal is overwhelmed by intrinsic cellular auto-fluorescence. This kit enables consistent, homogeneous staining results with very little fluorescence variation between cells in a population, so distinct generations can be seen without any requirement for complex modeling software.

Long-term signal retention
Unlike stains that label the lipid membrane of cells, CellTrace™ Far Red stain easily crosses the plasma membrane and covalently binds inside cells where the stable, well-retained fluorescent dye offers a consistent signal, even after several days in a cell culture environment. CellTrace™ Far Red dye binds covalently to all free amines on the surface and inside of cells and shows little cytotoxicity, with minimal observed effect on the proliferative ability or biology of cells.

Easy multiplexing with other fluorophores
The red excitation at 630 nm and emission at 661 nm of CellTrace™ Far Red dye make it ideal for multiplexing due to the limited spectral overlap with other common dyes (Alexa Fluor™ 488, FITC, and RPE) and fluorescent proteins (Green Fluorescent Protein (GFP) and mCherry).

Simple, robust staining protocol
The CellTrace™ Far Red Cell Proliferation Kit contains convenient single-use vials of dry dye to permit small-scale experiments without preparing excess quantities of dye. A stock solution is prepared by dissolving the contents of a vial in anhydrous DMSO prior to use. To stain 1 mL of cells in protein-free medium, 1 μL of this stock solution is typically used. Cells should be stained for 20 minutes at room temperature with gentle agitation. A brief wash with complete medium will then quench any dye remaining in solution.
For Research Use Only. Not for use in diagnostic procedures.
사양
검출 방법Fluorescence
염료 유형Contains 1 vial of CellTrace™ Far Red dye and 1 vial of DMSO (100μL)
형태Solid
형식Tube(s)
수량20 Assays
시약 유형CFSE & Related Compounds
배송 조건Room Temperature
용해도DMSO (Dimethylsulfoxide)
Emission633
용도 (장비)Flow Cytometer
제품라인CellTrace
제품 유형Cell Proliferation Kit
Unit SizeEach
구성 및 보관
Contains 1 vial of CellTrace™ Far Red dye and 1 vial of DMSO (100 μL).
  • Store in freezer -5°C to -30°C.
  • 자주 묻는 질문(FAQ)

    I want to do a cell migration study for around 4 hours and need to fluorescently label the cells with a dye. What do you recommend?

    Calcein, AM and FDA (fluorescein diaceate) are examples of some dyes used for this application. Since these dyes are not incorporated or covalently attached to any cellular components, they may have a short retention time as some cell types may actively efflux the dye out of the cells. The CellTracker and CellTrace dyes include either a mild thiol-reactive chloromethyl group or amine-reactive succinnimidyl ester group to allow for covalent binding to cellular components, providing for better retention. As with any reagent, one should empirically determine retention times for the cell type used.

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

    I labeled my cells with Calcein, AM, but when I imaged the next day, there was no fluorescence from Calcein. Why?

    Calcein, AM is a good choice for cell tracking and as a general cytoplasmic stain. However, it doesn't bind to anything and may be actively pumped out of the cells within a couple hours, which is likely what happened. The retention of Calcein within live cells is dependent upon the inherent properties of the cell type and culture conditions.

    For long-term imaging, you may wish to consider a reactive cytoplasmic stains such as CFDA, SE or the CellTracker and CellTrace dyes.

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

    Can the CellTrace Far Red dye be fixed with paraformaldehyde (PFA)?

    Yes, the CellTrace Far Red dye can be fixed with paraformaldehyde (PFA). The dye covalently binds to cells and will not wash out after permeabilization or fixation.

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

    I would like to label two cell populations with two different CellTrace reagents and then co-culture these cells. Will the CellTrace reagent leave the cells to stain other cells?

    We have not tested the use of the CellTrace reagents for co-culture applications. In theory, this may work, but you would have to test this on your cells of interest.

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

    With the CellTrace cell proliferation kits, for flow cytomtery, I am getting only one broad peak on my histogram instead of multiple peaks. What is causing this?

    A single broad peak is usually caused by using too high a concentration of dye and/or too long an incubation time.

    Find additional tips, troubleshooting help, and resources within our Flow Cytometry Support Center.

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