This bisbenzimide dye, Hoechst 34580, is related to the important minor-groove binding, dsDNA-selective dyes Hoechst 33258 and Hoechst 33342. HoechstRead more
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Catalog number H21486
Price (USD)
276.00
Each
Add to cart
Price (USD)
276.00
Each
Add to cart
This bisbenzimide dye, Hoechst 34580, is related to the important minor-groove binding, dsDNA-selective dyes Hoechst 33258 and Hoechst 33342. Hoechst 34580 has somewhat longer-wavelength spectra than the other Hoechst dyes when bound to nucleic acids [Howard Shapiro, personal communication].
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Excitation Wavelength Range392⁄440
Dye TypeHoechst 34580
FormatTube(s)
For Use With (Equipment)Fluorescence Microscope
Quantity5 mg
Detection MethodFluorescence
FormSolid
Shipping ConditionRoom Temperature
Solubilitywater, DMF or DMSO (Dimethylsulfoxide)
Product TypeNucleic Acid Stain
SubCellular LocalizationNucleic Acids, Nucleus
Unit SizeEach
Contents & Storage
Contains 1 vial of Hoechst 34580 (5 mg). Store in freezer -25°C and protect from light.
Frequently asked questions (FAQs)
Is DAPI a good live-cell nuclear label?
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.
I want to label the nuclei of live cells and track them over time. Can I use DAPI for this?
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.
DAPI and Hoechst dyes are quite similar to each other. Why would I choose one over the other?
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.