Hoechst 33258 analog 2

CAS No. 23491-54-5

Hoechst 33258 analog 2 ( —— )

Catalog No. M27036 CAS No. 23491-54-5

Hoechst 33258 analog 2 is part of a family of blue fluorescent dyes used to stain DNA.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    Hoechst 33258 analog 2
  • Note
    Research use only, not for human use.
  • Brief Description
    Hoechst 33258 analog 2 is part of a family of blue fluorescent dyes used to stain DNA.
  • Description
    Hoechst 33258 analog 2 is part of a family of blue fluorescent dyes used to stain DNA.(In Vitro):The dyes Hoechst 33258 and Hoechst 33342 are the ones most commonly used and they have similar excitation/emission spectra. Both dyes are excited by ultraviolet light at around 350 nm, and both emit blue/cyan fluorescent light around an emission maximum at 461 nm. Unbound dye has its maximum fluorescence emission in the 510-540 nm range. Hoechst dyes are soluble in water and in organic solvents such as dimethylformamide or dimethyl sulfoxide. Concentrations can be achieved of up to 10 mg/mL. Aqueous solutions are stable at 2-6 °C for at least six months when protected from light. For long-term storage, the solutions are instead frozen at ≤-20 °C. Although the dyes can bind to all nucleic acids, AT-rich double-stranded DNA strands enhance fluorescence considerably. Hoechst dyes are cell-permeable and can bind to DNA in live or fixed cells.
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    BCRP; Parasite
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    23491-54-5
  • Formula Weight
    422.5
  • Molecular Formula
    C26H26N6
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    CN1CCN(CC1)c1ccc2nc([nH]c2c1)-c1ccc2nc([nH]c2c1)-c1cccc(C)c1
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Robinson MW, et, al. The comparative metabolism of triclabendazole sulphoxide by triclabendazole-susceptible and triclabendazole-resistant Fasciola hepatica. Parasitol Res. 2004 Feb;92(3):205-10.
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