DAPI is stable in dilute solutions, and can be added directly to antifade mounting medium for long-term use; we also offer EverBrite™ Mounting Media with DAPI (see Below we provide two protocols for staining live cells with DAPI or Hoechst. Certificate No. Wegen seiner geringen kurzfristigen Giftigkeit kann Hoechst 33342 (und ähnliche Farbstoffe wie Hoechst 33258 oder H 34580) [3] zur Zellzahlkontrolle in Lebendzell-Experimenten eingesetzt werden.
2013 Jan;139(1):195-204. doi: 10.1007/s00418-012-1039-8. Please enable it to take advantage of the complete set of features! This property has been used to identify Q-bands in chromosomes (Q-bands: AT-rich chromosome regions … Mit Hoechst 33342 angefärbte Zellkerne der Larven von Platynereis dumerilii. Direct addition of 10X probe is a convenient staining method that doesn’t require medium exchange, but care must be taken to mix immediately yet gently to avoid high transient probe concentration or disruption of cells by pipetting. Hoechst 33528 is slightly more water soluble than Hoechst 33342, but both dyes are highly cell membrane permeant and widely used in cell cycle studies and as nuclear counterstains for live or fixed cells. They are typically used for staining at 1 ug/mL. However, for some cell types, morphology or viability may be affected by medium exchange. 1985 Jan;60(1):7-11. doi: 10.3109/10520298509113885. A comparison of four DNA stains considered to be AT-specific with chromosomes from a clonal Chinese hamster cell line B14F28-C5 have been made. … DAPI is somewhat less cell membrane permeant than Hoechst dyes, and must be used at a higher concentration (usually 10 ug/mL) for live cell staining. It emits blue fluorescence light around an emission maximum at 461 nm when bound to DNA. Hoechst 33342 binds preferentially to adenine-thymine (A-T) regions of DNA. DAPI staining is specific and highly reproducible in this line. DAPI. The UV-excited fluorescent dye DAPI has been used as a cell marker since the 1980s [3]. All payment in US dollars must be payable on a US bank. Staining by medium exchange results in uniform exposure of cells to probe. Nuclear Stains & DNA/RNA Dyes It can be used for fixed cell staining at 1 ug/mL. These include Hoechst 33342, Hoechst 33258, 4′,6-diamidino-2-phenylindole (DAPI), mithramycin, propidium iodide, 7-amino-actinomycin D, SYTOX green, DRAQ5, and TO-PRO-3 iodide. They are typically used for staining at 1 ug/mL. Authors F Otto, K C Tsou. Endogenous nuclear topoisomerase I activity in HL-60 cells was inhibited by treatment with Hoechst 33342 but not Hoechst 33258. Therefore, they can be used to stain cells without a wash step. Note that we do not recommend adding highly concentrated dye directly to cells in culture, as this will result in local areas of high dye exposure. This site needs JavaScript to work properly. Epub 2015 Jun 24.Jaworska A, Wojcik T, Malek K, Kwolek U, Kepczynski M, Ansary AA, Chlopicki S, Baranska M.Mikrochim Acta.
We offer a wide selection of fluorescent organelle stains and other probes for live or fixed cells. PMID: 2579484 DOI: 10.3109/10520298509113885 Abstract A comparison of four DNA stains considered to be AT-specific with chromosomes from a clonal Chinese hamster cell line B14F28-C5 have been made. The staining is very stable and non-toxic to live cells for several days or longer.DAPI and Hoechst are minor-groove binding dyes; DAPI has higher affinity for A/T-rich regions of DNA than G/C-rich DNA. Since the Hoechst 33342 dye is specific for DNA binding, ribonuclease treatment is not needed to avoid nonspecific RNA staining. Epub 2019 May 15.Biol Reprod.
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