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SCT047

BioTracker Cystine-FITC Live Cell Dye

Live cell imaging dye that measures cystine uptake at the single cell level used to detect glutathione (GSH) synthesis, reactive oxygen species (ROS) detoxification, T-cell activation and B-cell development.

Sinónimos:

Cellular cystine uptake detection, Live cell imaging probe

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NACRES:
NA.47
UNSPSC Code:
12352207
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assay

≥98% (H-NMR), ≥98% (HPLC), ≥98% (LC/MS), ≥98% (elemental analysis)

technique(s)

cell based assay: suitable

detection method

fluorometric

shipped in

ambient

storage temp.

-10 to -25°C

General description

Uptake of cystine allows accumulation of cysteine that is necessary for glutathione synthesis and reactive oxygen species (ROS) detoxification. After the uptake of cystine into the cytoplasm, the reducing intracellular environment leads to a separation of one cystine molecule into two cysteine molecules. A key function of cysteine is to maintain the cellular pools of glutathione (GSH). Cystine uptake is also required for T-cell activation and B-cell development.

The BioTracker Cystine-FITC dye is a live cell green fluorescent imaging probe that measures cystine uptake at the single cell level. The probe has been used to measure T-cell activation using traditional and imaging flow cytometry methods.

Spectral Properties
Absorbance: 450nm
Emission: 525nm

Application

Live cell fluorescent imaging
Research Category
Cell Imaging
Research Sub Category
Live Cell Dye

Physical form

Lyophilized

Preparation Note

Store BioTracker Cystine-FITC Live Cell Dye at -20°C, desiccate and protect from light
Note: Centrifuge vial briefly to collect contents at bottom of vial before opening.

Analysis Note

Purity: ≥ 98% confirmed by HNMR, LC-MS and HPLC and elemental analysis
Molar Mass: 625.65 g/mol

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Este artículo
SCT046SCT044SCT059
technique(s)

cell based assay: suitable

technique(s)

cell based assay: suitable

technique(s)

cell based assay: suitable

technique(s)

cell based assay: suitable

storage temp.

-10 to -25°C

storage temp.

-10 to -25°C

storage temp.

-10 to -25°C

storage temp.

-

assay

≥98% (H-NMR), ≥98% (LC/MS), ≥98% (HPLC), ≥98% (elemental analysis)

assay

≥98% (H-NMR), ≥98% (HPLC), ≥98% (LC/MS), ≥98% (elemental analysis)

assay

≥98% (H-NMR), ≥98% (HPLC), ≥98% (LC/MS), ≥98% (elemental analysis)

assay

≥98% (H-NMR), ≥98% (HPLC), ≥98% (LC/MS), ≥98% (elemental analysis)

shipped in

ambient

shipped in

ambient

shipped in

ambient

shipped in

-

detection method

fluorometric

detection method

fluorometric

detection method

fluorometric

detection method

fluorometric


Clase de almacenamiento

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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Peter J Siska et al.
Journal of immunological methods, 438, 51-58 (2016-09-07)
T and B lymphocytes undergo metabolic re-programming upon activation that is essential to allow bioenergetics, cell survival, and intermediates for cell proliferation and function. To support changes in the activity of signaling pathways and to provide sufficient and necessary intracellular



Número de artículo de comercio global

SKUGTIN
SCT04704054839532412

Questions

  1. How should I dissolve the reagent when I want to add it to the cell experiment?

    1 answer
    1. The following protocol is recommended:
      1. Before opening the vial, spin down the solid to the bottom by a
      microcentrifuge or by a desktop centrifuge.
      2. Warm the vial to room temperature and add DMSO to prepare a
      1000X stock solution of 1-5 mM (freeze aliquots at -20°C).
      3. Dilute in cell culture media at a final concentration of 1-5 µM and add
      to cells in culture. Incubate at 37°C for 20-45 minutes.
      4. Wash cells with PBS buffer before imaging.

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