CellTrace™ Yellow Cell Proliferation Kit, for flow cytometry
CellTrace™ Yellow Cell Proliferation Kit, for flow cytometry
Invitrogen™

CellTrace™ Yellow Cell Proliferation Kit, for flow cytometry

CellTrace™ Yellow Cell Proliferation Kit is used for in vitro and in vivo labeling of cells to trace multiple generationsRead more
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Catalog NumberQuantity
C3457320 Assays
C34567180 Assays
Catalog number C34573
Price (MXN)
-
Quantity:
20 Assays

CellTrace™ Yellow Cell Proliferation Kit is used for in vitro and in vivo labeling of cells to trace multiple generations using dye dilution by flow cytometry. This reagent is specifically designed for excitation by either a 532-nm or 561-nm laser, and it can be easily multiplexed with reagents and antibodies excited by other commonly used lasers.

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
Simple—robust staining protocol

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 Yellow 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 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 Yellow 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 Yellow 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 yellow excitation at 546 nm and emission at 579 nm of CellTrace Yellow dye make it ideal for multiplexing due to the limited spectral overlap with other common dyes (e.g., Alexa Fluor™488 and FITC) and green fluorescent protein (GFP) .

Use the SpectraViewer to help you plan your experiments.

Simple, robust staining protocol
The CellTrace Yellow 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.
Specifications
Detection MethodFluorescence
Dye TypeCellTrace™ Yellow
FormSolid
FormatTube(s)
Quantity20 Assays
Reagent TypeCFSE & Related Compounds
Shipping ConditionRoom Temperature
SolubilityDMSO (Dimethylsulfoxide)
Emission579
Excitation Wavelength Range532 or 561, 532
For Use With (Application)Proliferation Assay
For Use With (Equipment)Flow Cytometer
Product LineCellTrace
Product TypeCell Proliferation Kit
Unit SizeEach
Contents & Storage
  • 1 vial CellTrace™ Yellow Dye
  • 100 μL DMSO
  • Store in freezer (-5°C to -30°C)

Frequently asked questions (FAQs)

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.

What cellular components do the CellTrace Proliferation dyes label?

The dyes provided in the CellTrace Proliferation kits are amine-reactive dyes that are considered general cytoplasmic stains. They may bind to various membrane proteins, organelles as well as components in the cytoplasm. They are not known to localize in any specific organelles.

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

With the CellTrace Yellow Cell Proliferation Kit, for flow cytometry, I do not see a clear discrimination between generations, only a single broad peak. Why is this occurring?

A single broad peak may be observed if the dye concentration used is too high or if the dye incubation period is too long. We recommend reducing the amount of dye used and/or the incubation period.

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

When would I use CellTrace Yellow Dye?

We recommend using the CellTrace Yellow Dye if you have either a 532 or 561 nm laser available on your flow cytometer and you want to use the other lasers and channels for other commonly used fluorophores.

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

Citations & References (6)

Citations & References
Abstract
Deriving Quantitative Cell Biological Information from Dye-Dilution Lymphocyte Proliferation Experiments.
Authors:Roy K, Shokhirev MN, Mitchell S, Hoffmann A,
Journal:Methods Mol Biol
PubMed ID:29388101
'The dye-dilution assay is a powerful tool to study lymphocyte expansion dynamics. By combining time course dye-dilution experiments with computational analysis, quantitative information about cell biological parameters, such as percentage of cells dividing, time of division, and time of death, can be produced. Here, we describe the method to generate ... More
Triple co-culture of human alveolar epithelium, endothelium and macrophages for studying the interaction of nanocarriers with the air-blood barrier.
Authors:Costa A, de Souza Carvalho-Wodarz C, Seabra V, Sarmento B, Lehr CM,
Journal:Acta Biomater
PubMed ID:31004840
'Predictive in vitro models are valuable alternatives to animal experiments for evaluating the transport of molecules and (nano)particles across biological barriers. In this work, an improved triple co-culture of air-blood barrier was set-up, being exclusively constituted by human cell lines that allowed to perform experiments at air-liquid interface. Epithelial NCI-H441 ... More
Isolation and Activation of Murine Lymphocytes.
Authors:Lim JF, Berger H, Su IH
Journal:J Vis Exp
PubMed ID:27842342
'B and T cells, with their extremely diverse antigen-receptor repertoires, have the ability to mount specific immune responses against almost any invading pathogen(1,2). Understandably, such intricate abilities are controlled by a large number of molecules involved in various cellular processes to ensure timely and spatially regulated immune responses(3). Here, we ... More
Superior properties of CellTrace Yellow™ as a division tracking dye for human and murine lymphocytes.
Authors:Tempany JC, Zhou JH, Hodgkin PD, Bryant VL,
Journal:Immunol Cell Biol
PubMed ID:29363164
The discovery of cell division tracking properties of 5-(and-6)-carboxyfluorescein diacetate succinimidyl ester (CFSE) by Lyons and Parish in 1994 led to a broad range of new methods and numerous important biological discoveries. After labeling, CFSE is attached to free amine groups and intracellular proteins in the cytoplasm and nucleus of ... More
Autoreactive, Low-Affinity T Cells Preferentially Drive Differentiation of Short-Lived Memory B Cells at the Expense of Germinal Center Maintenance.
Authors:Jain RW, Parham KA, Tesfagiorgis Y, Craig HC, Romanchik E, Kerfoot SM,
Journal:Cell Rep
PubMed ID:30566861
B cell fate decisions within a germinal center (GC) are critical to determining the outcome of the immune response to a given antigen. Here, we characterize GC kinetics and B cell fate choices in a response to the autoantigen myelin oligodendrocyte glycoprotein (MOG) and compare the response with a standard ... More