Hoechst 33342

製品コードS0485 バッチS048501

印刷

化学情報

 Chemical Structure Synonyms Pibenzimol, bisBenzimide H 33342, HOE 33342, HO342 Storage
(From the date of receipt)
3 years -20°C powder
化学式

C27H28N6O

分子量 452.55 CAS No. 23491-52-3
Solubility (25°C)* 体外 Water 90 mg/mL (198.87 mM)
DMSO 10 mg/mL (22.09 mM)
Ethanol Insoluble
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.

溶剤液(一定の濃度)を調合する

生物活性

製品説明 Hoechst 33342 (Pibenzimol, bisBenzimide H 33342, HOE 33342, HO342) is a membrane-permeant fluorescent stain that can stain live cells. Hoechst 33342 binds to adenine-thymine-rich regions of DNA in the minor groove and greatly increases the fluorescence. It allows easy visualization of the nucleus in interphase cells and chromosomes in mitotic cells.
in vitro

1.1 Preparation of the stock solution
Dissolve 10 mg of Hoechst in 5 mL DMSO
Note: It is recommended to store the stock solution at 4℃ or -20℃ away from light and avoid repetitive freeze-thaw cycles.
1.2 Preparation of Hoechst working solution
Dilute the stock solution in serum-free cell culture medium or PBS to obtain final concentration 10 μg/mL Hoechst working solution.
Note: Please adjust the concentration of Hoechst working solution according to the actual situation.
1.Cell staining
2.1 Suspension cells(6-well plate)
a. Centrifuge at 1000 g at 4℃ for 3-5 minutes and then discard the supernatant. Wash twice with PBS, 5 minutes each time. The cell density is 1×106/mL.
b. Add 1 mL of working solution, and then incubate at room temperature for 3-10 minutes.
c. Centrifuge at 400 g at 4℃ for 3-4 minutes and then discard the supernatant.
d. Wash twice with PBS, 5 minutes each time.
e. Resuspend cells with serum-free cell culture medium or PBS. Observation by fluorescence microscopy or flow cytometry.
2.2 Adherent cells
a. Culture adherent cells on sterile coverslips.
b. Remove the coverslip from the medium and aspirate excess medium.
c. Add 100 μL of working solution, gently shake it to completely cover the cells,and then incubate at room temperature for 3-10 minutes.
d. Wash twice with medium, 5 minutes each time.Observation by fluorescence microscopy or flow cytometry.

プロトコル(参考用のみ)

Selleckの高級品が、幾つかの出版された研究調査結果(以下を含む)で使われた:

Novel therapeutic targets, including IGFBP3, of umbilical cord mesenchymal stem cell-conditioned medium in intrauterine adhesion [ Biol Open, 2024, bio.060141] PubMed: 38224009
Stress relief as a natural resilience mechanism against depression-like behaviors [ Neuron, 2023, S0896-6273(23)00668-2] PubMed: 37776853
Low-dose X-ray irradiation combined with FAK inhibitors improves the immune microenvironment and confers sensitivity to radiotherapy in pancreatic cancer [ Biomed Pharmacother, 2022, 151:113114] PubMed: 35594704
A Novel Polysaccharide From Chuanminshen violaceum and Its Protective Effect Against Myocardial Injury [ Front Nutr, 2022, 9:961182] PubMed: 35911096

長期の保管のために-20°Cの下で製品を保ってください。

人間や獣医の診断であるか治療的な使用のためにでない。

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