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Merck

PKH67GL

Kit linker cellulare PKH67 fluorescente verde per la marcatura generale della membrana cellulare

Distributed for Phanos Technologies

Sinonimo/i:

Green PKH membrane labeling kit

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1 KIT

1.820,00 €

1.820,00 €


Per informazioni sulla disponibilità, contatta il Servizio Clienti.


Informazioni su questo articolo

NACRES:
NA.32
UNSPSC Code:
12352207

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Nome del prodotto

Kit linker cellulare PKH67 fluorescente verde per la marcatura generale della membrana cellulare, Distributed for Phanos Technologies

packaging

pkg of 1 kit

storage condition

protect from light

fluorescence

λex 490 nm; λem 502 nm (PKH67 dye)

detection method

fluorometric

shipped in

ambient

storage temp.

room temp

Quality Level

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Questo articolo
MINI67PKH26GLMINI26
packaging

pkg of 1 kit

packaging

pkg of 1 kit

packaging

pkg of 1 kit

packaging

pkg of 1 kit

storage condition

protect from light

storage condition

protect from light

storage condition

protect from light

storage condition

protect from light

fluorescence

λex 490 nm; λem 502 nm (PKH67 dye)

fluorescence

λex 490 nm; λem 502 nm (PKH67 dye)

fluorescence

λex 551 nm; λem 567 nm (PKH26 dye)

fluorescence

λex 551 nm; λem 567 nm (PKH26 dye)

detection method

fluorometric

detection method

fluorometric

detection method

fluorometric

detection method

fluorometric

shipped in

ambient

shipped in

ambient

shipped in

ambient

shipped in

ambient

storage temp.

room temp

storage temp.

room temp

storage temp.

room temp

storage temp.

room temp

Application

Il kit PKH67 Green Fluorescent Cell Linker per la marcatura aspecifica della membrana cellulare è stato utilizzato:
  • per marcare e quindi studiare gli esosomi espulsi dalle cellule nel cancro della mammella triplo negativo[1]
  • per marcare le cellule apoptotiche[2] al fine di studiare il ruolo del recettore ανβ5 nel legame e nell′internalizzazione delle cellule apoptotiche[3]
  • nell′imaging in fluorescenza.[4]

Il kit serve alla marcatura generale delle membrane cellulari. Il PKH67 ha una coda di carbonio alifatica più lunga del PKH1 e del PKH2, gli altri due coloranti verdi precedentemente descritti per il tracking cellulare in vitro e in vivo. Sulla base della maggiore lunghezza della coda, gli studi in-house hanno mostrato costantemente un trasferimento cellula-cellula ridotto per il PKH67 rispetto al PKH2.
È stata osservata una lenta perdita di fluorescenza negli studi condotti in vivo con PKH1 e PKH2. Il PKH67 può mostrare proprietà simili dal momento che questo comportamento sembra essere caratteristico dei coloranti linker cellulari verdi ma non di quelli rossi. La correlazione tra la ritenzione della membrana cellulare in vitro e l′emivita della fluorescenza in vivo nelle cellule che non si dividono prevede un′emivita della fluorescenza in vivo di 10-12 giorni per il PKH67. Altri coloranti linker cellulari con emivite analoghe sono stati utilizzati per monitorare il traffico di linfociti e macrofagi in vivo nell′arco di 1-2 mesi. Questo suggerisce che il PKH67 potrebbe essere utile anche per gli studi di tracking in vivo di durata moderata.

Other Notes

Per ulteriori dettagli tecnici sui coloranti linker cellulari fluorescenti PKH e CellVue®, inclusa un′ampia bibliografia, fare clic qui.

Legal Information

CellVue is a registered trademark of Phanos Technologies

pictograms

FlameExclamation mark

signalword

Danger

hcodes

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2

Classe di stoccaggio

3 - Flammable liquids

flash_point_f

57.2 °F - closed cup

flash_point_c

14 °C - closed cup


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Exosomes from triple-negative breast cancer cells can transfer phenotypic traits representing their cells of origin to secondary cells
O Brien K, et al.
European Journal of Cancer, 49(8), 1845-1859 (2013)
Anjali P Kusumbe et al.
Stem cells (Dayton, Ohio), 27(3), 498-508 (2009-03-04)
Recruitment and localization of endothelial precursors within tumors is a potential area for the development of therapeutics, because their functional contribution to tumor vasculature is realized to be important for cancer cell survival. However, the exact nature of the recruited
Hybrid microscaffold-based 3D bioprinting of multi-cellular constructs with high compressive strength: A new biofabrication strategy
Yu Jun T, et al.
Scientific Reports, 6, 39140-39140 (2016)
Dandan Ma et al.
Cells, 9(4) (2020-04-01)
Human salivary histatin 1 (Hst1) and Hst2 exhibit a series of cell-activating properties (e.g., promoting adhesion, spreading, migration and metabolic activity of mammalian cells). In contrast, Hst5 shows an anti-fungal property but no cell-activating properties. Previous findings suggest that their
alpha v beta 5 integrin recruits the CrkII-Dock180-Rac1 complex for phagocytosis of apoptotic cells
Albert, Matthew L and Kim, Jong-Ii and Birge, Raymond B
Nature Cell Biology, 2(12), 899-899 (2000)

Articoli

Lipophilic cell tracking dyes enable cancer biologists to track tumor and immune cell functions both in vitro and in vivo. Read the article to choose a right membrane dye kit for cell tracking and proliferation monitoring.

Optimal staining is a key component for studying tumorigenesis and progression. Learn useful tips and techniques for dye applications, including examples from recent studies.

PKH and CellVue® Fluorescent Cell Linker Kits provide fluorescent labeling of live cells over an extended period of time, with no apparent toxic effects.

PKH dyes are easy to use and achieve stable, uniform, and reproducible fluorescent labeling of live cells. PKH dyes are non-toxic membrane stains which produce high signal to noise ratio.

Domande

1–10 di 12 domande  
  1. I mark mitochondria for injection with PKH26 Red Fluorescent Cell Linker Kit for General Cell Membrane Labeling. I want to use another dye to mark another type of mitochondria and inject them together in the same fish egg. Is PKH67 ok for this like PKH26?

    1 risposta
    1. Yes, Product PKH67 would be suitable for this application. In this paper, both Products PKH26 and PKH67 are used in a similar application:
      https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5679712/

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  2. What can be the alternative for removing excess dye after labeling of exosomes using PKH67 dye apart from ultracentrifugation?

    1 risposta
    1. Excess dye is bound to serum or albumin which is added to the cell/dye mixture as a stop reaction. The recommended clean up or dye removal is by standard centrifugation (400 x g for 10 minutes, wash, and repeat). See the Product Information Sheet, page 3, bullet point 8 for more information:
      https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/product/documents/984/984/pkh67glbul.pdf

      Alternate methods for excess dye removal have not been investigated.

      Utile?

  3. Can we remove the excess PKH67 DYE used for the labeling of exosomes using exosome spin column rather than ultracentrifugation.

    1 risposta
    1. The recommended exosome labeling protocol has been optimized to assure the best possible results. The use of exosome spin columns with the PKH and CellVue products has not been validated. See below for a link to our exosome labeling protocol. A spin column method may not offer the best results.

      https://www.sigmaaldrich.com/technical-documents/protocol/cell-culture-and-cell-culture-analysis/imaging-analysis-and-live-cell-imaging/exosome-labeling-pkh

      Utile?

  4. When using Product PKH67GL, PKH67 Green Fluorescent Cell Linker Kit for General Cell Membrane Labeling, how long will the cells remain stained after treatment?

    1 risposta
    1. Labeled cells that have been washed can be visualized in culture up to 100 days after staining (for non-dividing cells). The dye itself is stable and will divide equally when the cells divide. After staining with PKH dyes, you can observe as many as 8 divisions depending on how brightly the cells were stained initially and the amount of surface area on the cells. Most commonly, 4-6 divisions can be visualized.

      Utile?

  5. What is the excitation and emission spectra for Product PKH67GL, Green Fluorescent Cell Linker Kit?

    1 risposta
    1. The spectra can be found on the product insert.The product has a maximum excitation at 490 nm and maximum emission at 502 nm.

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  6. Are cells lost during the PKH67 Green Fluorescent Cell Linker Kit for General Cell Membrane Labeling staining process?

    1 risposta
    1. Over-labeling of the cells will result in loss of membrane integrity and reduced cell recovery.  Methods for improving cell viability can be found on the troubleshooting guide.

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  7. What method of fixation can be used for tissue/cells with the PKH Fluorescent Cell Linker Kit for General Cell Membrane Labeling dyes?

    1 risposta
    1. A protocol for visualization of tissue sections can be found in the technical bulletin.  For visualization of stained cells by immunofluorescence or flow cytometry, the cells can be fixed in 2% paraformaldehyde for 15 minutes. The use of other organic solvents will extract the dye from the cells.  If internal labeling is desired, the cells can be permeabilized with saponin (50-75 μg/mL). Here is the link to the Troubleshooting Guide.

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  8. Will Product PKH67, Green Fluorescent Cell Linker Kit, stain dead cells?

    1 risposta
    1. As long as the cell has an intact membrane, the PKH76 dye can label the cell.

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  9. What is the difference between Green Fluorescent Cell Linker Kits PKH2 and PKH67?

    1 risposta
    1. PKH2 was one of the early PKH dyes.  The PKH67 dye has a longer aliphatic tail.  There is reduced cell-celldye transfer for PKH67 as compared with PKH2.

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  10. How many cells can be stained with Product PKH67GL, Green Fluorescent Cell Linker Kit?

    1 risposta
    1. This kit can stain 50 × 107 cells if used as directed (1 × 107 cells stained with 2 × 10-6 M PKH67).

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