Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Catalog Number | Quantity | Product Type | Dye Type |
---|---|---|---|
H3570 | 10 mL | Nucleic Acid Stain | Hoechst 33342, trihydrochloride trihydrate |
62248 | 1 mL | DAPI | DAPI |
D21490 | 10 mg | DAPI | DAPI, FluoroPure grade |
D3571 | 10 mg | DAPI | DAPI |
D1306 | 10 mg | DAPI | DAPI |
H3569 | 10 mL | Nucleic Acid Stain | Hoechst 33258, pentahydrate (bis-benzimide) |
H1398 | 100 mg | Nucleic Acid Stain | Hoechst 33258, pentahydrate (bis-benzimide) |
H21491 | 100 mg | Nucleic Acid Stain | Hoechst 33258, pentahydrate (bis-benzimide), FluoroPure grade |
62249 | 5 mL | Nucleic Acid Stain | Hoechst 33342 |
H1399 | 100 mg | Nucleic Acid Stain | Hoechst 33342, trihydrochloride trihydrate |
H21492 | 100 mg | Nucleic Acid Stain | Hoechst 33342, trihydrochloride trihydrate, FluoroPure grade |
DAPI is a fluorescent dye commonly used in molecular biology and cell biology research. DAPI is known for its ability to bind to DNA, specifically to the minor groove of double-stranded DNA. This dye emits blue fluorescence when excited by ultraviolet light, allowing researchers to visualize and stain DNA in various biological samples.
Hoechst dyes are DNA-specific fluorescent stains that bind to the minor groove of double-stranded DNA. They emit blue fluorescence when excited by ultraviolet light. These dyes are widely used for staining DNA in various biological samples.
The FluoroPure™-grade of Hoechst and DAPI powders are manufactured using stringent purification processes to minimize impurities that could interfere with fluorescence imaging. This ensures that the DAPI and Hoechst provides reliable and consistent results with minimal background noise. The >98% purity of FluoroPure grade reagents make them particularly suitable for demanding applications such as super-resolution microscopy and live-cell imaging, where precise and accurate visualization of DNA is essential.
DAPI (4',6-Diamidino-2-Phenylindole):
DAPI 4',6-diamidino-2-phenylindole is a blue fluorescent probe that fluoresces brightly upon selectively binding to the minor groove of double stranded DNA, where its fluorescence is approximately 20-fold greater than in the non-bound state. Its selectivity for DNA and high cell permeability allows efficient staining of nuclei with little background from the cytoplasm and efficient contrasting in IHC staining and spatial transcriptomics and proteomics tissue imaging. DAPI is a classic nuclear counterstain for immunofluorescence microscopy, as well as an important component of high-content screening methods requiring cell-based quantitation of DNA content and segmentation (ex/em 341/452 nm).
DAPI as a dilactate powder is more water soluble than the dihydrochloride salt, and therefore a better choice for preparing stock solutions in water.
To make a 5 mg/mL DAPI stock solution (14.3 mM for the dihydrochloride or 10.9 mM for the dilactate), dissolve the contents of one vial (10 mg) in 2 mL of deionized water (dH2O) or dimethylformamide (DMF). The less water-soluble DAPI dihydrochloride may take some time to completely dissolve in water and sonication may be necessary.
Note: Neither of these DAPI derivatives is very soluble in PBS for Stock Solution.
Dilute the DAPI Stock Solution 1:5000 (or 1:1000 for the 1 mg/mL DAPI 62248) in ultrapure water or PBS (1 μg/mL DAPI). Filter the working solution to remove dye aggregates that can result in punctate signal.
Hoechst 33342, Trihydrochloride, Trihydrate and Hoechst 33258, Pentahydrate (bis-Benzimide):
Our Hoechst dyes are renowned fluorophores widely used for DNA staining in both living and fixed cells. With their exceptional affinity and specificity towards DNA, these dyes serve as excellent targeting agents that can be conjugated to various molecules, allowing them to be tethered to DNA.
The Hoechst dyes typically include Hoechst 33258, Hoechst 33342, and Hoechst 34580. Developed by the German company Hoechst AG in the early 1970s, these bisbenzimide dyes have been widely used for DNA staining ever since.
Excited by UV light, Hoechst dyes emit a broad spectrum of blue light. Upon binding to DNA, their fluorescence increases approximately 30-fold, ensuring a strong signal-to-noise ratio. This fluorescence enhancement is the result of suppressed rotational relaxation and hydration reduction upon DNA binding (ex/em 360/460 nm).
Hoechst dyes are non-intercalating, binding specifically to the minor groove of DNA at A–T-rich regions. This unique binding mechanism allows for precise and reliable DNA staining.
Whether you're working with living or fixed cells, our Hoechst dyes are compatible with immunohistochemistry applications. Additionally, the binding of Hoechst 33342 to DNA induces minimal cytotoxicity, ensuring the viability of your cells.
While all three Hoechst dyes have similar applications, they do possess slight differences in their properties. Hoechst 33342, for example, is significantly more cell-permeable due to the addition of a lipophilic ethyl group, making it the preferred choice for living cell staining. On the other hand, Hoechst 34580, with its dimethylamine group instead of the phenol, exhibits a shifted emission maximum at 490 nm, compared to the 461 nm of Hoechst 33258 and Hoechst 33342.
Hoechst 33258, Pentahydrate is also known as bis-Benzimide.
Application of DAPI and Hoechst Fluorescent Dyes:
DAPI is considered a semi-permeant/impermeant nucleic acid stain. Staining of nucleic is dependent upon the cell line in its performance. Some cell lines will label with DAPI, others not at all, and others label inconsistenly. Instead, we recommend using either Hoechst 33342 or Hoechst 33258, which have the same wavelength and binding mode as DAPI (at the A-T minor groove) but are readily cell-permeant.
Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.
You can use a combination of two dyes with overlapping blue emission. For cytoplasm, you can label the cell with CellTracker Blue CMAC. This can be combined with Hoechst 33342 for nuclei. Both dyes are imaged using a standard DAPI filter set.
Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.
We do not recommend doing this. DAPI is considered to be a semi-permeant/impermeant nucleic acid stain. DAPI staining of live cells may be inconsistent. It is best used as a counterstain for fixed samples. Other cell permeable nucleic acid stains, such as Hoechst or the SYTO dyes may affect cellular function.
For mammalian cells, we recommend using the CellLight Nucleus transduction reagents, available in CFP, GFP and RFP. With these reagents, the cells are transduced overnight in a single labeling step and the next day the nuclei will fluoresce. The label may be retained for 3-5 days and should not affect cell function. Cytoplasmic cell tracking dyes such as the CellTracker dyes may also be used.
Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.
Platelet cells don't have DNA, while bacteria do. Therefore, a cell-permeant, DNA-selective dye would preferentially stain the bacteria with limited staining of the platelets. We recommend using Hoechst 33342 dye.
Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.
DAPI is a very common blue-fluorescent dye for nuclear counterstaining and gives very bright labeling on nuclei in fixed and permeabilized cells and tissues. However, it is considered to be a semi-permeant to impermeant stain and provides inconsistent staining of live cells. Hoechst 33342 dye is cell-permeant and stains with the same binding mechanism and fluorescent color; it is preferred for live-cell imaging and is just as good as DAPI for fixed cell labeling.
Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.
Share catalog number, name or link