CellVue® Burgundy Cell Labeling Kit

GPR: General Purpose Reagents. For Laboratory Use.

SKU# 88-0872

Cat. No. Size
88-0872-16 Mini
88-0872-17 Midi
Please inquire about custom configurations or bulk packaging.

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Data for CellVue® Burgundy Cell Labeling Kit.

Labeling of mouse spleen cells with 2 µM CellVue® Burgundy for 5 minutes at room temperature in...View More

  • Data for CellVue® Burgundy Cell Labeling Kit.
Description

Description: CellVue® dyes are lipophilic dyes that can be used to label the cell membrane for the purpose of identifying and tracking labeled cells. Cell labeling is rapid and stable and can be combined with fluorescently labeled antibodies and other markers of cellular function for flow cytometric analysis and fluorescent microscopy. Mini CellVue® Kits are supplied with one vial of dye stock (1 mM in ethanol) and one vial of labeling vehicle (Diluent C); Midi CellVue® Kits are supplied with two vials of dye stock (1 mM in ethanol) and six vials of Diluent C.

CellVue® Burgundy is a far-red/near-infrared fluorescent cell labeling reagent. It is optimally excited at 683 nm and has a peak emission of 707 nm. CellVue® Burgundy can be excited by the red laser line (633 nm), however, it can be detected equally in filter sets designed for Alexa Fluor® 700 and APC-eFluor® 780 or similar fluorochromes. Therefore, it is not recommended to use antibodies conjugated to these fluorochromes when using CellVue® Burgundy. CellVue® Burgundy can be used in combination with APC.

Details
Legal CellVue® is a trademark of PTIR.
Reported Applications Flow Cytometric Analysis, Immunocytochemistry, Microscopy, Cell Labeling
Documentation
TDS Link Download TDS
References

References: Roy EJ, Sivaguru M, Fried G, Gray BD, Kranz DM. Imaging membrane intercalating near infrared dyes to track multiple cell populations. J Immunol Methods. 2009 Aug 31;348(1-2):18-29.

Westhorpe CL, Zhou J, Webster NL, Kalionis B, Lewin SR, Jaworowski A, Muller WA, Crowe SM. Effects of HIV-1 infection in vitro on transendothelial migration by monocytes and monocyte-derived macrophages. J Leukoc Biol. 2009 Jun;85(6):1027-35.


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