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DAPI Staining Kit

Catalog Number: orb219885

DispatchUsually dispatched within 5-10 working days
$ 90.00
Catalog Numberorb219885
CategoryTools
DescriptionDAPI (4',6-diamidino-2-phenylindole) is a blue-fluorescent DNA stain that exhibits -20-fold enhancement of fluorescence upon binding to AT regions of dsDNA.It is used extensively in fluorescence microscopy. As DAPI can pass through an intact cell membrane, it can be used to stain both live and fixed cells, though it passes through the membrane less efficiently in live cells and therefore the effectiveness of the stain is lower.
Tested applicationsICC, IF
StorageStore at -20°C for one year.
NoteFor research use only
Application notesDAPI (4,6-diamidino-2-phenylindole) is a cell permeable fluorescent minor groove-binding probe for DNA. It binds to the double-stranded DNA (especially to AT rich DNA), and forming a stable fluoresces complex. DAPI throughout the live and dead cell membrane that can be utilized for DAN detect for chromosome DAN, Yeast DNA, chloroplast DNA, Virus DNA and so on. DAPI-DNA complex shows light blue flourescence color with excitation light 364 nm and emission light 454 nm.Experiment Notes: This product is 1 mg/ml Chromogen. Solute it with suitable density for applies. Recommend density for tissue staining is 1-2 ug/ml (on the 0.5 ug/ml, flourescence become light saturation). For cell culture the density is 0.1 ug/ml.
Expiration Date12 months from date of receipt.

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Huanli Zhao 1, Xuejun Wu 2, Shumeng Yang 3, Lili Jiang 4, Huiying Yu 3, Yubin L Formononetin Alleviates the Inflammatory Response Induced by Carotid Balloon Injury in Rats via the PP2A/MAPK Axis Immunol Invest, (2025)

Applications

IF

Reactivity

Rat

M El Assar, B García-Gómez, JM La Fuente, M Alonso-Isa, JI Martínez-Salamanca Targeting TRPC-5 Channel Inhibition to Improve Penile Vascular Function in Erectile Dysfunction International Journal of Molecular Sciences, (2025)

DAPI Staining Kit

Immunofluorescent analysis staining in HeLa cells. Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with the primary antibody in 3% BSA-PBS and incubated overnight at 4 °C in a humidified chamber. Cells were washed with PBST and incubated with a FITC-conjugated secondary antibody (green) in PBS at room temperature in the dark. DAPI was used to stain the cell nuclei (blue).