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CFSE Cell Division Tracker Kit

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  • ¥1190
  • biolegend
  • 423801
  • 美国
  • 2025年07月14日
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    • 文献和实验
    • 技术资料
    • 英文名

      CFSE Cell Division Tracker Kit

    • 库存

      大量

    • 供应商

      上海研卉生物科技

    • 规格

      1 kit

    CFSE Cell Division Tracker Kit
    Other Names
    5-(and 6)-Carboxyfluorescein diacetate succinimidyl ester Kit, CFDA SE Kit
    Description

    CFSE Cell Division Tracker Kit is composed of 5 vials, 100 µg per vial of CFSE (formally known as 5-(and 6)-Carboxyfluorescein diacetate succinimidyl ester of CFDA SE), and 500 µl of anhydrous DMSO. CFSE is able to passively diffuse into cells. Inside the cell, its acetate groups are cleaved by intracellular esterases, and the molecules are converted to fluorescent esters. CFSE is retained within the cell and covalently couples to intracellular molecules via its succinimidyl group. Due to this covalent coupling reaction, fluorescent CFSE can be retained within the cell for an extremely long period. Also, due to this stable linkage, once the dye has been incorporated within the cell, it is not transferred to adjacent cells. CFSE is widely used for cell proliferation assays and in vivo cell tracking.

    Preparation
    The CFSE Cell Division Tracker Kit is composed of lyophilized CFSE and anhydrous DMSO. For reconstitution, bring the kit to room temperature; add 36 µl of DMSO to one vial of CFSE dye until fully dissolved.
    Storage & Handling
    Store CFSE Cell Division Tracker Kit at -20°C upon receipt. Do not open vials until needed. Once the DMSO is added to the CFSE, use immediately, or store at -20°C in a dry place and protected from light, preferably in a dessicator or in a container with desiccant for no more than one month.
    Application

    ICFC - Quality tested
    In vivo cell tracking1 - Reported in the literature, not verified in house

    Recommended Usage

    This lot has been tested by flow cytometric analysis of in vitro cell proliferation assay. It can be used at concentrations ranging from 0.5 - 10 µM for cell labeling. It is recommended that the reagent be titrated for optimal performance for each cell type, culturing condition, or application.

    Application Notes

    The molecular weight of CFSE is 557.47. The excitation and emission wavelengths of CFSE-labeled cells are 492 nm and 517 nm, respectively. Each 100 µg vial of CFSE may be reconstituted with 36 µl of anhydrous DMSO to yield a stock concentration of 5 mM.

    Materials Provided:
    5 vials x 100 µg CFSE
    500 µl anhydrous DMSO

    CFSE Labeling Procedure:
    1. Prior to reconstitution, spin down the vial of lyophilized reagent in a microcentrofuge to ensure the reagent is at the bottom of the vial.
    2. Prepare stock solution by reconstituting 1 vial of lyophilized CFSE dye in 36 µL of DMSO to make a 5 mM solution.
    3. Prepare a 5 µM working solution by diluting 1 µL of 5 mM CFSE stock solution in 1 mL PBS for every 1 mL of cell suspension (or at an optimal working concentration as determined by titration).
    4. Spin down and resuspend cells at 10-100 x 106 cells/mL in the CFSE working solution.
    5. Incubate cells for 20 minutes at room temperature or 37°C and keep protected from light.
    6. Quench the staining by adding 5 times the original staining volume of cell culture medium containing 10% FBS.
    7. Pellet cells and resuspend in pre-warmed cell culture medium.
    8. Incubate cells for 10 minutes.
    9. After incubation, CFSE labeled cells are ready for downstream applications or analysis.

    Additional Product Notes

    View more applications data for this product in our Scientific Poster Library.


    Watch a Scientific Poster video of this product.

    Application References

    (PubMed link indicates BioLegend citation)
    1. Parish CR, et al. 2009. Curr. Protoc. Immunol. Unit4.9.
    2. Miller MJ, et al. 2002. Science 296:1869.
    3. Tai LH, 2013. Clin Cancer Res. 19:5104. PubMed
    4. Svajger U, et al. 2014. J Lukoc Biol. 95:33. PubMed
    Product Citations
    1. Soloff A, et al. 2017. J Appl Toxicol. 10.1002/jat.3465. PubMed
    2. Zupancic E, et al. 2017. Journal of Controlled Release. 10.1016/j.jconrel.2017.05.014. PubMed
    3. Nenasheva T, et al. 2017. PLoS One. 12(6):e0178983. PubMed
    4. Hawila E, et al. 2017. Cell Rep.. 10.1016/j.celrep.2017.10.104. PubMed
    5. Shifrut E et al. 2018. Cell. 175(7):1958-1971 . PubMed
    6. Page N, et al. 2018. Immunity. 48:937. PubMed
    7. Timilshina M, et al. 2020. Cell Reports. 27(10):2948-2961.e7.. PubMed
    8. Krueger CC, et al. 2019. Front Immunol. 10:1831. PubMed
    9. Kwee BJ, et al. 2019. Sci Adv. 5:eaav6313. PubMed
    10. Montel‐Hagen A et al. 2019. Cell stem cell. 24(3):376-389 . PubMed
    11. Sen S, et al. 2018. J Immunol. 201:440. PubMed
    12. Georgouli M et al. 2019. Cell. 176(4):757-774 . PubMed

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