Hoechst 33258

Discontinued Product

5824 has been discontinued.
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Hoechst 33258 | CAS No. 23491-45-4 | Fluorescent DNA Stains
1 Image
Description: Fluorescent dye for staining DNA

Chemical Name: 4-[6-(4-Methyl-1-piperazinyl)[2,6'-bi-1H-benzimidazol]-2'-yl]phenol trihydrochloride

Purity: ≥98%

Product Details
Citations (2)
Reviews

Biological Activity

Hoechst 33258 is a fluorescent dye. Binds the minor groove of DNA at A and T rich regions. Can be used as indicator of apoptosis.

Optical Data for Hoechst 33258

λabs 352 nm
λem 461 nm
Application Flow Cytometry

Plan Your Experiments

Use our spectra viewer to interactively plan your experiments, assessing multiplexing options. View the excitation and emission spectra for our fluorescent dye range and other commonly used dyes.

Spectral Viewer

Spectral Viewer

Technical Data

M.Wt:
533.88
Formula:
C25H24N6O.3HCl
Solubility:
Soluble to 20 mM in DMSO and to 100 mM in water
Purity:
≥98%
Storage:
Store at -20°C
CAS No:
23491-45-4

The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.

Product Datasheets

Reconstitution Calculator
Molarity Calculator

Reconstitution Calculator

The reconstitution calculator allows you to quickly calculate the volume of a reagent to reconstitute your vial. Simply enter the mass of reagent and the target concentration and the calculator will determine the rest.

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Molarity Calculator

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*When preparing stock solutions always use the batch-specific molecular weight of the product found on the vial label and CoA (available online).

Citations for Hoechst 33258

The citations listed below are publications that use Tocris products. Selected citations for Hoechst 33258 include:

2 Citations: Showing 1 - 2

  1. Mitotic replisome disassembly depends on TRAIP ubiquitin ligase activity.
    Authors: Moreno Et al.
    Life Sci Alliance  2019;2
  2. CXCR4/SDF1 signalling promotes sensory neuron clustering in vitro.
    Authors: Terheyden-Keighley Et al.
    Biol Open  2018;7

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