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Hoechst 33258 trihydrochloride

,23491-45-4
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  • ¥435 - 1084
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  • HY-15558A
  • 2025年12月05日
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    • 文献和实验
    • 技术资料
    • 保存条件

      4°C, sealed storage, away from moisture and light

    • 英文名

      bisBenzimide H 33258 trihydrochloride; H 33258 trihydrochloride

    • 库存

      货期:1-2天

    • 供应商

      MedChemExpress LLC

    • CAS号

      23491-45-4

    • 规格

      10 mM * 1 mL/25 mg/50 mg/100 mg

    规格:10 mM * 1 mL产品价格:¥820.0
    规格:25 mg产品价格:¥435.0
    规格:50 mg产品价格:¥623.0
    规格:100 mg产品价格:¥1084.0

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    Hoechst 33258 trihydrochloride

    CAS No. : 23491-45-4

    MCE 国际站:Hoechst 33258 trihydrochloride

    产品活性:Hoechst 33258 trihydrochloride 是 Hoechst 系列的标记染料。Hoechst 系列是活细胞核标记染料。Hoechst 通过结合 DNA 双链中的小沟而结合核酸。Hoechst 倾向于结合富含 A/T 的 DNA 链。同时,富含 A/T 的双链 DNA 使荧光强度显著增强。Hoechst 可穿过细胞膜,结合活细胞或固定细胞。Hoechst 染料的荧光强度随着溶液 pH 升高而增强。

    研究领域:Others

    作用靶点:Fluorescent Dye

    In Vitro: Preparation of Hoechst working solution
    1.1 Preparation of stock solution
    Take 10 mg and dissolve in 5 mL DMSO
    Note: It is recommended that the stock solution be stored at 4℃ or - Store at 20℃ in the dark and avoid repeated freezing and thawing.
    1.2 Preparation of Hoechst working solution
    The diluted stock solution was dissolved in serum-free cell culture medium or PBS to obtain Hoechst working solution with a final concentration of 10 μg/mL.
    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 for 3-5 min at 4℃ and discard the supernatant. Wash 2 times with PBS, 5 minutes each. The cell density was 1×106/mL.
    b. Add 1 mL of working solution and incubate at room temperature for 3-10 minutes.
    c. Centrifuge at 400 g for 3-4 minutes at 4℃ and discard the supernatant.
    d. Wash 2 times with PBS, 5 min each.
    e. Resuspend cells in serum-free cell culture medium or PBS. Fluorescence microscopy or flow cytometry observation.
    2.2 Adherent cells
    a. Adherent cells were cultured on sterile coverslips.
    b. Remove the coverslip from the medium and aspirate excess medium. c. Add 100 μL of working solution, shake gently to completely cover the cells, and incubate at room temperature for 3-10 minutes.
    d. Wash 2 times with medium, 5 min each. Fluorescence microscope or flow cytometry observation.

    Store
    4°C, 1 year. Avoid light

    Precautions
    1. Please adjust the concentration of Hoechst working solution according to the actual situation.
    2. This product is for R&D use only, not for medicine, household or other purposes.
    3. For your safety and health, please wear a lab coat and disposable gloves for operation.

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    图标文献和实验
    相关实验
    • Hoechst 33258染色

      Hoechst 33258染色1.原理 Hoechst 33258Hoechst 33342均为非嵌人性荧光染料。它们在活细胞中 DNA聚AT序列富集区域的小沟处与DNA结合。活细胞或固定细胞均可从低浓度溶液中 摄取该染料。从而使细胞核着色。故又把此类染料称为DNA探针。Hoechst 33342和Hoechst 33258均可溶于水并在水溶液中保持稳定。Hoechsr-DNA的激发和发射波长分别550nm和460nm。在荧光显微镜紫外光激发时,Hoechst-DNA发出亮

    • Testing for Mycoplasma by Indirect DNA Stain (Hoechst 33258 stain)

      Materials Media� pre-warmed to 37ºC (refer to the ECACC Cell Line Data Sheet for the correct medium) 70% ethanol in water (Prod. No. R8382 ) Methanol (Prod. No. 175 ) Acetic Acid Glacial (Prod. No. A6283 ) Hoechst 33258

    • Vital Staining of Chromosomes with Hoechst 33258

        Vital Staining of Chromosomes with Hoechst 33258 Materials 1. Hoechst 33258, 10 mg/ml stock in DMSO. 2. Culture medium. 3. 15 ml sterile conical tube. Procedure 1. In a 15 ml conical tube, add 1 volume Hoechst 33258

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