This product will not prevent mitosis. However, if verapamil is used during the experiment (included in the kit to help with probe retention), it can inhibit mitosis in a dose-dependent manner.
SCT120
Colorante per nuclei verde BioTracker 488
Live cell imaging green nuclear staining dye with greater photostability than traditional blue fluorescent nuclear stains such as DAPI and Hoechst 33342.
Sinonimo/i:
Live cell imaging probe, Live cell nuclear imaging probe
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368,00 €
Spedizione prevista il28 aprile 2025Dettagli
Scegli un formato
About This Item
368,00 €
Spedizione prevista il28 aprile 2025Dettagli
Prodotti consigliati
tecniche
cell based assay: suitable
Metodo di rivelazione
fluorometric
Condizioni di spedizione
ambient
Descrizione generale
Il colorante verde per nuclei BioTracker 488 è un colorante per il DNA verde, fluorescente e permeabile alla membrana cellulare che colora specificamente i nuclei delle cellule sia vive che fissate. Ha un'eccellente specificità per il DNA, non richiede passaggi di lavaggio ed ha una bassa tossicità, per consentire l'imaging delle cellule vive. E′ fornito con un flaconcino di verapamil, un inibitore della pompa di efflusso che può aiutare a migliorare la ritenzione del colorante e la colorazione delle cellule vive in alcuni tipi cellulari.
N.B.: Il colorante nucleare BioTracker mostra anche una fluorescenza blu nel canale DAPI, e potrebbe non essere adatto per l'imaging multicolore con sonde blu.
Proprietà spettrali
Assorbanza: 500 nm
Emissione: 515 nm
Applicazioni
Imaging di cellule
Colorante per cellule vive
Componenti
2) 1 provetta da100µL di Verapamil HCL (100mM in DMSO) (CS224592)
Qualità
Assorbanza: 500 nm
Emissione: 515 nm
Stato fisico
Stoccaggio e stabilità
N.B: prima dell′apertura, centrifugare brevemente per raccogliere il contenuto sul fondo della provetta.
Esclusione di responsabilità
Avvertenze
Warning
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Acute Tox. 4 Oral - Aquatic Chronic 2
Codice della classe di stoccaggio
10 - Combustible liquids
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Could the BioTracker 488 Green Nuclear Dye SCT120 prevent mitosis in 2D in vitro cultures?
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Does the fluorescence intensity increase by chromosome condensation similarly to DAPI or Hoechst?
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This product has not been tested for an increase in fluorescence intensity with chromosome condensation.
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Is there any toxicity data available for extended (>48h) live cell staining?
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The dye with verapamil showed no obvious toxicity in MCF-7 cells over the course of 72 hours. It may be different for different cell lines and different experimental conditions.
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Is it possible to use SCT120 BioTracker 488 Green Nuclear Dye and PKH26 Red Fluorescent Cell Linker for in vivo applications, and what is their stability duration?
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The PKH series of dyes are designed for membrane labeling and can be used to track cells through several divisions. The intensity of the dye decreases by half with each cell division, so the duration of visibility will depend on the cell division rate of the specific cell type.
Regarding SCT120 nuclear dye, there is limited information about the viability of cells after staining or the photostability of the dye once the cells have been stained.
Currently, there is no available information on the compatibility or effects of using SCT120 in conjunction with PKH26GL for dual staining of cells.
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How can I optimize staining using SCT120?
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The recommended protocol for using SCT120 is as follows:
1. Dilute the BioTracker™ Nuclear Dye from its 1000X stock solution to a working concentration of 1X in cell culture medium. To achieve this, one could add 1 µL of dye to 1 mL of culture medium. It is important to note that the optimal concentration of the probe may vary depending on the cell type. Optionally, verapamil can be included in the staining solution to enhance probe retention in live cells. The ideal concentration of verapamil will likely be different across cell types, and it is suggested to test concentrations ranging from 10-100 µM.
2. Discard the culture medium from the cells and replace it with the diluted BioTracker™ Nuclear Dye solution. Incubate the cells at 37°C for a minimum of 10 minutes.
To optimize staining, consider the following adjustments:
• Probe Dilution: Although the standard dilution is 1:1000, experimenting with other dilutions such as 1:500 or 1:750 could be beneficial. Observe the results and, if necessary, test additional dilutions to find the most effective concentration.
• Verapamil Concentration: The suggested range for verapamil is between 10 to 100 µM. Trial with two or three different dilutions within this spectrum may help to refine the staining process.
• Incubation Time: Initially, a 10-minute incubation is recommended. However, extending this period to 20, 40, or even 60 minutes at 37°C could improve staining results. If positive changes are noted, further experimentation with the duration may be warranted to optimize the staining signal.
It is vital to only change one variable at a time during these optimizations. Altering multiple factors simultaneously, such as the dye dilution, verapamil concentration, and incubation time, would make it difficult to identify which specific change led to any observed improvements. Additionally, checking cell viability before staining is advisable. Using Trypan Blue to determine cell viability might provide insights into the overall health and suitability of the cells for staining.
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Will SCT120, BioTracker 488 Green Nuclear Dye SCT work with the FITC channel?
Will SCT120, BioTracker 488 Green Nuclear Dye SCT work with the FITC channel?
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Yes, for SCT120 we do recommend analyzing the cells using the FITC channel.
Please refer to the product's data sheet, found in the DOCUMENTATION section of the Product Detail Page: https://www.sigmaaldrich.com/product/mm/sct120#product-documentation
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Could you please provide the chemical structure and formula for BIOTRACKER 488 GREEN NUCLEAR DYE, if available?
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This information is considered proprietary.
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Hi I was wondering if this stain would work in a 100% alcoholic liquid, or whether it requires protons to fluoresce?
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The dye has not been validated for DNA binding under 100% alcoholic liquid. It does not require protons to fluoresce.
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